MEDICAL BULLETIN BOARD

Redhill Biopharma Extends Talicia® Unrestricted National and Regional Commercial Coverage to over 40 Million Additional Americans

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Talicia® unrestricted access in the U.S. now extends to over 70% of commercial lives covered Approximately 35% of Americans are affected by H. pylori infection, a Group 1 carcinogen and the strongest risk factor for gastric cancer; eradication of H. pylori has been shown to reduce the risk of gastric cancer by up to 75% Talicia addresses the high and growing resistance of H. pylori bacteria to commonly used antibiotics

TEL AVIV, Israel and RALEIGH, N.C., RedHill Biopharma Ltd. (Nasdaq: RDHL) (“RedHill” or the “Company”), a specialty biopharmaceutical company, today announced that it has increased unrestricted national and regional commercial coverage for Talicia® (omeprazole magnesium, amoxicillin and rifabutin)[i] to more than 40 million additional Americans.

“With this addition of unrestricted coverage for over 40 million more lives, Talicia is now available to over 70% of commercial lives. The unrestricted commercial coverage achieved for Talicia to date far exceeds our expectations at such an early stage following the product’s launch. We continue to work diligently to increase unrestricted coverage of Talicia, in an effort to make a significant difference in ending sub-optimal treatment of H. pylori,” said Rick Scruggs, RedHill’s Chief Commercial Officer. “Antibiotic resistance is a major issue in the treatment of H. pylori infections and yet, despite current guideline recommendations from the American College of Gastroenterology calling for use of the most effective first-line treatment, physicians are still prescribing treatment regimens containing antibiotics such as clarithromycin that face high levels of bacterial resistance. This growth in unrestricted commercial access helps change that dynamic by increasing access to Talicia to more than 167 million Americans.”

RedHill has previously announced listings of Talicia as a preferred brand on the national formularies of Prime Therapeutics, EnvisionRx, and Express Scripts.

About Talicia
(omeprazole magnesium, amoxicillin and rifabutin)

Talicia is the only rifabutin-based therapy approved for the treatment of H. pylori infection and is designed to address the high resistance of H. pylori bacteria to clarithromycin-based standard-of-care therapies. The high rates of H. pylori resistance to clarithromycin have led to significant rates of treatment failure with clarithromycin-based standard-of-care therapy and are a strong public health concern, as highlighted by the FDA and the World Health Organization (WHO) in recent years.

Talicia is a novel, fixed-dose, all-in-one oral capsule combination of two antibiotics (amoxicillin and rifabutin) and a proton pump inhibitor (PPI) (omeprazole). In November 2019, Talicia was approved by the U.S. FDA for the treatment of H. pylori infection in adults. In the pivotal Phase 3 study, Talicia demonstrated 84% eradication of H. pylori infection in the intent-to-treat (ITT) group vs. 58% in the active comparator arm (p<0.0001). Minimal to zero resistance to Talicia was detected in RedHill’s pivotal Phase 3 study. Further, in an analysis of data from this study, it was observed that subjects who were confirmed adherent[ii] to their therapy had response rates of 90.3% in the Talicia arm vs. 64.7% in the active comparator arm[iii].

Talicia is eligible for a total of eight years of post-approval U.S. market exclusivity under both its Qualified Infectious Disease Product (QIDP) designation and New Clinical Investigation exclusivities. In addition, Talicia is protected by a robust U.S. patent portfolio which provides patent protection until at least 2034, with additional patents and applications pending and granted in various territories worldwide.

About H. pylori

H. pylori bacterial infection affects approximately 35%[iv] of the U.S. population, with an estimated two million patients treated annually[v]. Worldwide, more than 50% of the population is affected by H. pylori infection, which is classified by the WHO as a Group 1 carcinogen, remains the strongest known risk factor for gastric cancer[vi] and a major risk factor for peptic ulcer disease[vii] and gastric mucosa-associated lymphoid tissue (MALT) lymphoma[viii]. More than 27,000 Americans are diagnosed with gastric cancer annually[ix], while eradication of H. pylori has been shown to reduce the risk of gastric cancer by up to 75%[x]. Eradication of H. pylori is becoming increasingly difficult, with current standard-of-care therapies failing in approximately 25-40% of patients who remain H. pylori-positive due to high resistance of H. pylori to antibiotics commonly used in standard combination therapies[xi].

About RedHill Biopharma

RedHill Biopharma Ltd. (Nasdaq: RDHL) is a specialty biopharmaceutical company primarily focused on gastrointestinal and infectious diseases. RedHill promotes the gastrointestinal drugs, Movantik® for opioid-induced constipation in adults[xii], Talicia® for the treatment of Helicobacter pylori (H. pylori) infection in adults[xiii], and Aemcolo® for the treatment of travelers’ diarrhea in adults[xiv]. RedHill’s key clinical late-stage development programs include: (i) RHB-204, with an ongoing Phase 3 study for pulmonary nontuberculous mycobacteria (NTM) disease; (ii) opaganib (Yeliva®), a first-in-class SK2 selective inhibitor targeting multiple indications with a Phase 2/3 program for COVID-19 and Phase 2 studies for prostate cancer and cholangiocarcinoma ongoing; (iii) RHB-104, with positive results from a first Phase 3 study for Crohn’s disease; (iv) RHB102 (Bekinda®), with positive results from a Phase 3 study for acute gastroenteritis and gastritis and positive results from a Phase 2 study for IBS-D; (v) RHB-107 (upamostat), a Phase 2-stage serine protease inhibitor with a planned Phase 2/3 study in symptomatic COVID-19 and targeting multiple other cancer and inflammatory gastrointestinal diseases; and (vi) RHB-106, an encapsulated bowel preparation.

More information about the company is available at:
redhillbio.com

IMPORTANT SAFETY INFORMATION

Talicia contains omeprazole, a proton pump inhibitor (PPI), amoxicillin, a penicillinclass antibacterial, and rifabutin, a rifamycin antibacterial. It is contraindicated in patients with known hypersensitivity to any of these medications, any other components of the formulation, any other beta-lactams or any other rifamycins.

Talicia is contraindicated in patients receiving delavirdine, voriconazole or rilpivirine-containing products.

Serious and occasionally fatal hypersensitivity reactions have been reported with omeprazole, amoxicillin and rifabutin.

Acute Tubulointerstitial Nephritis has been observed in patients taking PPIs and penicillins.

Clostridioides difficile-associated diarrhea has been reported with use of nearly all antibacterial agents and may range from mild diarrhea to fatal colitis. Talicia may cause fetal harm and is not recommended for use in pregnancy. It may also reduce the efficacy of hormonal contraceptives. An additional non-hormonal method of contraception is recommended when taking Talicia. Talicia should not be used in patients with hepatic impairment or severe renal impairment.

Cutaneous lupus erythematosus and systemic lupus erythematosus have been reported in patients taking PPIs. These events have occurred as both new onset and exacerbation of existing autoimmune disease.

The most common adverse reactions (≥1%) were diarrhea, headache, nausea, abdominal pain, chromaturia, rash, dyspepsia, oropharyngeal pain, vomiting, and vulvovaginal candidiasis.

To report SUSPECTED ADVERSE
REACTIONS, contact RedHill Biopharma INC.
at 1-833-ADRHILL (1-833-237-4455) or FDA at
1-800-FDA-1088 or fda.gov/medwatch.

Full prescribing information for Talicia is
available at:
Talicia.com

This press release contains “forward-looking statements” within the meaning of the Private Securities Litigation Reform Act of 1995. Such statements may be preceded by the words “intends,” “may,” “will,” “plans,” “expects,” “anticipates,” “projects,” “predicts,” “estimates,” “aims,” “believes,” “hopes,” “potential” or similar words. Forward-looking statements are based on certain assumptions and are subject to various known and unknown risks and uncertainties, many of which are beyond the Company’s control and cannot be predicted or quantified, and consequently, actual results may differ materially from those expressed or implied by such forward-looking statements. Such risks and uncertainties including, without limitation, the risk that the Company will be unable to secure additional pharmacy benefit management’s formulary coverage for Talicia®, as well as other risks and uncertainties associated with (i) the initiation, timing, progress and results of the Company’s research, manufacturing, pre-clinical studies, clinical trials, and other therapeutic candidate development efforts, and the timing of the commercial launch of its products and ones it may acquire or develop in the future; (ii) the Company’s ability to advance its therapeutic candidates into clinical trials or to successfully complete its pre-clinical studies or clinical trials, including the development of a commercial companion diagnostic for the detection of MAP; (iii) the lack of sufficient financial resources which may result in material adverse impact on the Company’s research, manufacturing, preclinical studies, clinical trials, and other therapeutic candidate development activities including delay or termination of preclinical or clinical activities or of any other such activities (iv) the Company’s ability to advance its therapeutic candidates into clinical trials or to successfully complete its preclinical studies or clinical trials (v) the extent and number and type of additional studies that the Company may be required to conduct and the Company’s receipt of regulatory approvals for its therapeutic candidates, and the timing of other regulatory filings, approvals and feedback; (vi) the manufacturing, clinical development, commercialization, and market acceptance of the Company’s therapeutic candidates and commercial products; (vi) the Company’s ability to successfully commercialize and promote Talicia®, and Aemcolo® and Movantik®; (vii) the Company’s ability to establish and maintain corporate collaborations; (viii) the Company’s ability to acquire products approved for marketing in the U.S. that achieve commercial success and build its own marketing and commercialization capabilities; (ix) the interpretation of the properties and characteristics of the Company’s therapeutic candidates and the results obtained with its therapeutic candidates in research, pre-clinical studies or clinical trials; (x) the implementation of the Company’s business model, strategic plans for its business and therapeutic candidates; (xi) the scope of protection the Company is able to establish and maintain for intellectual property rights covering its therapeutic candidates and commercial products and its ability to operate its business without infringing the intellectual property rights of others; (xii) parties from whom the Company licenses its intellectual property defaulting in their obligations to the Company; (xiii) estimates of the Company’s expenses, future revenues, capital requirements and needs for additional financing; (xiv) the effect of patients suffering adverse experiences using investigative drugs under the Company’s Expanded Access Program; (xv) competition from other companies and technologies within the Company’s industry; and (xvi) the hiring and maintaining employment of executive managers. More detailed information about the Company and the risk factors that may affect the realization of forward-looking statements is set forth in the Company’s filings with the Securities and Exchange Commission (SEC), including the Company’s Annual Report on Form 20-F filed with the SEC on March 4, 2020. All forwardlooking statements included in this press release are made only as of the date of this press release. The Company assumes no obligation to update any written or oral forward-looking statement, whether as a result of new information, future events or otherwise unless required by law.

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MEDICAL BULLETIN BOARD

Fujifilm Earns Fda “breakthrough Device” Designation for Endosurgical Image Enhancement Technology

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Company announces development of new image processing technologies designed to enhance visualization during therapeutic procedures

Lexington, MA – FUJIFILM Medical Systems U.S.A., Inc., a leading provider of endoscopic imaging solutions, announced that the U.S. Food and Drug Administration (FDA) granted its Breakthrough Device Designation – reserved for medical devices that provide for more effective treatment or diagnosis of life-threatening or irreversibly debilitating diseases or conditions – for Fujifilm’s new, in-development, endoscopic light and image processing technology. Although not yet 510(k) cleared, the goal of Fujifilm’s indevelopment image processing technology is to arm surgeons with the resources needed to care for patients at risk for ischemic states of the gastrointestinal tract.

“Leveraging our 80+ year imaging legacy, we develop technologies designed to enhance visualization and guide healthcare providers as they make critical clinical decisions caring for their patients,” says Taisuke Fujita, General ManagerEndoscopy, FUJIFILM Medical Systems U.S.A., Inc. “We’re proud to receive this designation through the FDA’s Breakthrough Devices Program on the heels of several advancements in 2019, and we look forward to bringing more innovations to the endoscopic and endosurgical markets in the years to come.”

Fujifilm’s new image processing technology is being developed to enhance endosurgical visualization and will be an upgrade to the ELUXEO Surgical System-the company’s in-market video imaging system which leverages 4-LED multi-light technology to enable advanced visualization modes including White Light Endoscopy, Linked Color Imaging (LCI), and Blue Light Imaging (BLI). These imaging modes are designed to improve visualization, detection, and characterization during procedures.

In gastrointestinal procedures such as colorectal surgeries, anastomosis is performed following resections, sometimes resulting in a serious complication – anastomotic leaks. One of the major causes of anastomotic leaks is necrosis of ischemic tissue where the anastomosis is performed, and Fujifilm’s new technology is designed to assist physicians in identifying ischemic areas of tissue.

Anastomotic leaks can result in septic complications, and are shown to have a 10% higher mortality rate as compared to patients who did not develop anastomotic leaks (14% vs. 4%). In a Medicare data analysis of more than 200,000 patients who underwent colorectal surgery between January 1, 2013 and August 31, 2015, care admission costs for patients with anastomotic leaks were reported more than $30,500 greater and the length of stay was 12 days longer as compared to those without. The commercial analysis of both the bariatric and colorectal populations trended similarly to the Medicare population in regards to all outcomes measured. These staggering statistics have led industry to research and develop technologies to prevent and/or reduce anastomotic leaks.

“For decades Fujifilm has invested in the research and development of technologies to improve patient outcomes and reduce healthcare costs, and in recent years, we’ve elevated our focus in endosurgery,” says Stephen Mariano, Vice President of Global Endosurgical R&D, FUJIFILM Medical Systems U.S.A., Inc. “We look forward to working with the FDA as we prioritize the development and access of some of our exciting endosurgical innovations.”

About Fujifilm

FUJIFILM Medical Systems U.S.A., Inc. is a leading provider of innovative diagnostic imaging products and medical informatics solutions that meet and exceed the evolving needs of healthcare facilities today and into the future. It’s ever expanding medical imaging solutions span digital radiography (DR), detectors, portables and suites, mammography systems with digital breast tomosynthesis, computed tomography solutions for oncology and radiology applications, technologically advanced flexible and surgical endoscopy and fluoroscopy solutions. Fujifilm enables interoperability through its Systems Integration offering as well as its comprehensive, AI-supported Synapse® Enterprise Imaging portfolio, which includes the TeraMedica Division of Fujifilm. Fujifilm’s in vitro diagnostics (IVD) portfolio includes clinical lab reagents, and biomarkers to assess the risk for the development of hepatocellular carcinoma in patients with chronic liver disease. FUJIFILM Medical Systems U.S.A., Inc. is headquartered in Lexington, Massachusetts.

For more information, please visit:
fujifilmhealthcare.com

FUJIFILM Holdings Corporation, Tokyo, Japan, brings cutting edge solutions to a broad range of global industries by leveraging its depth of knowledge and fundamental technologies developed in its relentless pursuit of innovation. Its proprietary core technologies contribute to the various fields including healthcare, graphic systems, highly functional materials, optical devices, digital imaging and document products. These products and services are based on its extensive portfolio of chemical, mechanical, optical, electronic and imaging technologies. For the year ended March 31, 2020, the company had global revenues of $22.1 billion, at an exchange rate of 109 yen to the dollar. Fujifilm is committed to responsible environmental stewardship and good corporate citizenship.

For more information, please visit:
fujifilmholdings.com

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FROM THE LITERATURE

Cognitive Deficit and White Matter Changes in Celiac Disease

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To validate previous reports over the presence and prevalence of brain injury in patients with celiac disease, neuropsychological dysfunction in patients with celiac disease included in the National UK Biobank was carried out, containing experimental medical data from 500,000 adults in the United Kingdom.

Biobank participants with celiac disease (N = 104; mean age 63 years; 65% female) were matched with healthy individuals (N = 198; mean age 63 years; 67% female) for age, sex, level of education, body mass index and diagnosis of hypertension. All participants were otherwise healthy.

Scores were compared from five cognitive tests and multiple choice responses in 6 questions about mental health between groups using the t test and chi-squared analyses. Groupwise analyses of MRI brain data included a study of diffusion tensor imaging metrics (mean diffusivity, fractional anisotropy, radial diffusivity, axial diffusivity), voxelbased morphometry and Mann-Whitney U comparisons of Fazekas grades.

Compared with controlled individuals, participants with celiac disease had significant deficits in reaction time and significantly higher proportions had indications of anxiety, depression, thoughts of self-harm and healthrelated unhappiness. Tract-based spatial statistics analysis showed significantly increased axial diffusivity in widespread locations, demonstrating white matter changes in brains of participants with celiac disease. Voxel-based morphometry and Fazekas grade analyses did not differ significantly between groups.

It was concluded in an analysis of data from the UK Biobank that participants were found with celiac disease to have cognitive deficit, indications of worsened mental health, and white matter changes, based on analyses of brain images. These findings support the concept that celiac disease is associated with neurological and psychological features.

Croall, I., Sanders, D., Hadjivassiliou, M., Hoggard, N. “Cognitive Deficit and White Matter Changes in Persons With Celiac Disease: A Population-Based Study.” Gastroenterology 2020; Vol. 158, pp. 2112-2122.

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FROM THE LITERATURE

Family History of Colorectal Cancer and Prevalence of Advanced Colorectal Neoplasia in Screening

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To evaluate the clinical significance of family history (FH) of colorectal cancer (CRC) in first degree relatives (FDRs) in screening stratified by different age groups, investigation of the relationship between FH and the presence of advanced colorectal neoplasia (ACN), and screened individuals in different age groups were evaluated.

Data from screened individuals aged 40 to 45 years (N = 2263), and 55 to 69 years (N = 2621), who underwent their first-ever screening colonoscopy, were analyzed. The relationship between FH and ACN was examined and a multivariate logistic regression analysis incorporating other baseline characteristics was performed.

Among individuals age 40 to 55 years, the prevalence of ACN was significantly higher in 249 individuals with affected FDRs than in those without (5.6% vs 1.6%), with an adjusted odds ratio of 3.7. The prevalence was particularly high in those having FDRs with CRC mortality (7.3%). Among individuals age 55 to 69 years, the prevalence of ACN was not significantly different between 291 individuals with affected FDRs and those without (5.8% vs 5.8%). However, individuals with two FDRs with CRC and mortality showed a high prevalence of ACN (17.4% and 42.9%, respectively).

It was concluded that an FH of CRC in FDRs was associated with a higher prevalence of ACN in younger individuals with a particularly high impact of FH on CRC mortality. In contrast, the impact of FH was weaker in older individuals, except those having two FDRs with CRC on mortality.

Sekiguchi, M., Kakujawa, Y., Nakamura, K., et al. “Family History of Colorectal Cancer and Prevalence of Advanced Colorectal Neoplasia in Asymptomatic Screened Populations in Different Age Groups.” Gastrointestinal Endoscopy 2020; Vol. 91, pp. 1361-1370.

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FROM THE LITERATURE

Famotidine Use in COVID-19

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To compare outcomes in patients hospitalized with Coronavirus (COVID-19), receiving famotidine therapy with those not receiving famotidine, a retrospective, propensity-matched observational study of consecutive COVID-19 positive patients was carried out between 2/24/2020 and 5/13/2020.

Of 878 patients in the analysis, 83 (9.5%), received famotidine. In comparison to patients not treated with famotidine, the patients treated with famotidine were younger (63.5 vs. 67.5 years), but did not differ with respect to baseline demographics or preexisting comorbidities. Use of famotidine was associated with a decreased risk of in-hospital mortality (OR 0.37), and combined death or intubation (OR 0.47). Propensity score matching to adjust for age difference between groups did not alter the effect on either outcome. In addition, patients receiving famotidine despite lower levels of serum markers for severe disease, including lower median peak CRP levels (9.4 vs. 12.7 mg/ dL), lower median procalcitonin levels (0.16 vs. 0.30 ng/mL), and a nonsignificant trend to lower median mean ferritin levels (797.5 vs. 964 ng/mL).

Logistic regression analysis demonstrated that famotidine was an independent predictor of both lower mortality and combined death/ intubation, whereas older age, BMI greater than 30 kg, chronic kidney disease, national early warning score, and higher neutrophil/ lymphocyte ratio were all predictors of adverse outcomes.

It was concluded that famotidine use in hospitalized patients with COVID-19 is associated with a lower risk of mortality, lower risk of combined outcome of mortality and intubation, and lower levels of serum markers for severe disease in hospitalized patients with COVID-19.

Mather, J., Seip, R., McKay, R. “Impact of Famotidine Use on Clinical Outcomes of Hospitalized Patients With COVID-19.” American Journal of Gastroenterology 2020; Vol. 115, pp. 1617-1623.

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FROM THE LITERATURE

Minimally Invasive Endoscopic Management of Gastroesophageal Reflux

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Endoscopic management of gastroesophageal reflux disease (GERD) is being employed increasingly. A scoping review was published, assessing the volume of available evidence on the benefits of endoscopic and minimally invasive surgical therapies for GERD.

Criteria were used to perform an extensive literature search of data regarding the reported benefits of endoscopic therapies and GERD randomized control studies were utilized when available. However, data from observed observational studies were also reviewed.

A formal review of evidence was performed in 22 studies. Inclusion and exclusion criteria and study duration were noted and tabulated. Assessment of outcomes was based on symptoms and objective criteria reported by investigators reported outcomes for the interventions tabulated under the heading of subjective (symptom scores), quality of life metrics, and change in proton pump inhibitor use, objective metrics (pH parameters, endoscopic signs and lower esophageal sphincter pressure changes).

Adverse events were noted and tabulated. The majority of studies showed symptomatic and objective improvement of GERD with device therapies. Adverse events were minimal. However, normalization of acid exposure occurred in about 50% of patients and for some modalities, long-term durability is uncertain.

It was concluded that this scoping review revealed that the endoluminal and minimallyinvasive surgical devices for GERD therapy are a promising alternative to proton pump inhibitor therapy. Their place in the treatment algorithm for GERD will be better defined when important clinical parameters, especially durability of effect, are better understood.

Vaezi, M., Shaheen, N., Muthusamy, V. “State of Evidence in Minimally-Invasive Management of Gastroesophageal Reflux: Findings of a Scoping Review.” Gastroenterology 2020; Vol. 159, pp. 1504-1525.

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FROM THE LITERATURE

Response to Bariatric Surgery in Non-Alcoholic Steatohepatitis

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To determine the long-term effects of bariatric surgery for patients with non-alcoholic steatohepatitis (NASH), sequential liver samples were evaluated that were collected at the time of bariatric surgery and 1 and 5 years later to assess the long-term effects of that surgery in patients with NASH.

A prospective study of 180 severely obese patients with biopsy-proven NASH defined by the NASH clinical research network histologic scores was performed. Patients underwent bariatric surgery at a single center in France and were followed for 5 years. Liver samples were obtained from 125 of 169 patients (76%), having reached 1 year in 64 of 94 patients (68%), having reached 5 years after surgery. The primary endpoint was resolution of NASH without worsening of fibrosis at 5 years. Secondary endpoints were improvement in fibrosis (reduction of 1 or greater stage at 5 years and regression of fibrosis and NASH at 1 and 5 years).

At 5 years after bariatric surgery, NASH was resolved without worsening fibrosis in samples from 84% of patients (N=64). Fibrosis decreased compared with baselines, in samples from 70.2% of patients. Fibrosis disappeared from samples from 56% of all patients and from samples from 45.5% of patients with baseline bridging fibrosis. Persistence of NASH was associated with no decrease in fibrosis unless weight loss (reduction in BMI of 6.3 kg/m² in patients with persistent NASH vs. reduction of 13.4 kg/m² with resolution of NASH). Resolution of NASH was observed at 1 year after bariatric surgery in biopsies from 84% of patients with no significant recurrence between 1 and 5 years. Fibrosis began to decrease from year 1 after surgery and continued to decrease until 5 years.

It was concluded in a long-term followup study of patients with NASH who underwent bariatric surgery, observation revealed resolution of NASH in liver samples from 84% of patients 5 years later. The reduction of fibrosis is progressive, beginning the first year and continuing through 5 years.

Lassailly, G., Caiazzo, R., NtandjaWandji, L. et al. “Bariatric Surgery Provides Long-Term Resolution of Nonalcoholic Steatohepatitis and Regression of Fibrosis.” Gastroenterology 2020; Vol. 159, pp. 1290-1301.

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FROM THE LITERATURE

Hemochromatosis and Hepatic Malignancy

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The predominant cause of hereditary hemochromatosis is HFE p.C282Y homozygous pathogenic variant. Liver carcinoma and mortality risks are increased in individuals with clinically diagnosed hereditary hemochromatosis, but risks are unclear in mostly diagnosed HFE p.C282Y homozygousidentified community genotyping.

To estimate the incidence of primary hepatic carcinoma and death by HFE variant status, a cohort study of 451,186 UK Biobank participants of European ancestry aged 40 to 70 years old, followed up from baseline assessment (2006-2010), until January 2018 was carried out.

Men and women with HFE p.C282Y and p.H63D genotypes was compared with those with neither HFE variants. Two linked coprimary outcomes (incident primary liver carcinoma and death from any cause), were ascertained from followup by way of inpatient hospital records, national cancer registry, and death certificate records, and from primary care data among a subset of participants for whom data was available. Associations between genotype and outcomes were tested using Cox regression adjusted for age, assessment center, genotyping array, and population genetic substructure.

Kaplan-Meier lifetable probabilities of incident diagnoses were estimated from age 40 to 75 years by HFE genotype and sex. A total of 451,186 participants had a mean age of 56.8 years; 54.3% women, and were followed up for a median of 8.9 years. Among the 1294 male p.C282Y homozygotes, there were 21 incident hepatic malignancies, 10 of which were in participants without a diagnosis of hemochromatosis in baseline and pC2827 homozygous men had a higher risk of hepatic malignancies (HR 10.5), and all cause of mortality (N = 88; HR 1.2) compared with men with neither HFE variant.

In lifetable projections for male p.C282Y homozygotes to 75 years, the risk of primary hepatic malignancy was 7.2% compared with 0.6% for men with neither variant and the risk of death was 19.5%, compared with 15.1% among men with neither variant.

Among female p.C282Y homozygotes (N = 1596), there were 3 incident hepatic malignancies and 60 deaths, but the associations between homozygosity and hepatic malignancy and death were not statistically significant (HR 2.1 and 1.2, respectively).

It is concluded that among men with HFE p.C282Y homozygosity, there was a significant increased risk of incident primary hepatic malignancy and death. Compared with men without p.C282Y or p.H63D variant, there was not a significant association for women. The effects of early diagnosis and treatment require further research.

Atkins, J., Pilling, L., Masoli, J., et al. “Association of Hemochromatosis HFE pC282Y Homozygosity With Hepatic Malignancy.” JAMA 2020; Vol. 324, pp. 20, 2048-2057.

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FRONTIERS IN ENDOSCOPY, SERIES #68

Endoscopic Ultrasound Guided Tissue Acquisition from Unusual Targets:A Review of Less Commonly Biopsied Sites

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Since the first described case of endoscopic ultrasound fine needle aspiration (EUS-FNA) nearly 30 years ago, EUS guided tissue acquisition has become a preferable diagnostic method that allows for high resolution imaging of the gastrointestinal tract and nearby structures as well as the means for biopsy in real time. The aim of this review is to assess the diagnostic accuracy and safety profiles of less commonly biopsied sites under EUS guidance, which includes lesions of the head and neck, the lungs, the adrenal glands and the pelvis.

INTRODUCTION

Endoscopic guided ultrasound (EUS) has become an invaluable tool for providing highresolution imaging of the gastrointestinal tract as well as adjacent structures while providing the ability of real-time tissue acquisition via endoscopic ultrasound fine needle aspiration (EUS-FNA) and endoscopic ultrasound fine needle biopsy (EUSFNB). Common indications for EUS guided tissue acquisition include: pancreatic lesions, biliary strictures, liver lesions, mediastinal and abdominal lymph node assessment, splenic masses, and subepithelial gastrointestinal tumors.1 This article aims to review unusual or less common indications for EUS and unusual sites for EUS guided biopsies including head and neck masses, adrenal gland lesions, and lesions of the pelvis with a particular emphasis on diagnostic accuracy and safety profiles associated with tissue acquisition from these sites.

Head and Neck Malignancies

The utility and high diagnostic accuracy of EUS in detecting mediastinal masses has been welldescribed.2,3 However, there is less research regarding EUS-guided tissue acquisition in patients with lesions of the head and neck. Most research examining EUS-FNA in this region describes how EUS may be used to stage malignancies that originate in the head and neck. For example, one study showed that EUS-FNA may play a role in staging squamous cell carcinoma of the head and neck, and their mediastinal spread. The study included cancers originating in the salivary gland, oropharynx, larynx and thyroid. Although the study only included 17 patients, it found that EUS was able to diagnose and stage head and neck malignancies by demonstrating esophageal invasion, lymph node involvement and, on two occasions, provide the initial tissue diagnosis.4 Similarly, a prospective study conducted in Japan showed that EUS can have greater diagnostic specificity and accuracy than MRI or barium swallow study for assessing the esophopharyngeal involvement of thyroid cancer.5 Of the 52 patients included in this analysis, EUS had a specificity and accuracy of 82.9% and 82.7%, respectively, for determining invasion into the muscularis propria when compared to MRI (which had corresponding rates of 60% and 65.4%, respectively) or barium swallow study (58.8% and 60%, respectively).4 However, the authors noted that diagnostic accuracy was decreased for thyroid cancer invasion of the upper lobe.4

Another retrospective study of 100 cases analyzed the frequency of thyroid gland masses among patients undergoing routine EUS.6 Twelve cases were identified with abnormal lesions of the thyroid with three patients receiving a new diagnosis of thyroid cancer; two with papillary thyroid cancer and one with poorly differentiated thyroid cancer.5 Ultimately, the authors concluded that routine EUS examination of the thyroid should be performed to identify potentially unexpected thyroid lesions.

EUS-FNA can also be utilized to directly biopsy the thyroid gland itself. The authors of the aforementioned study noted that of their twelve identified cases, only two cases underwent EUSFNA. The remaining cases were either referred for transcutaneous ultrasound guided biopsy or followed clinically.5

A small number of case reports exist describing direct tissue acquisition from the thyroid gland via EUS-FNA. One representative case report describes a case of 3x4cm mass in the left thyroid lobe that was not amenable to conventional, transcutaneous ultrasound guided biopsy due to a large amount of adjacent blood vessels, per the authors report. The authors noted that technical success was achieved and the patient was diagnosed with Hurtle cell neoplasm of the thyroid.7 Another case report, published in 2004, described a patient with a 5.7cm x 3.9cm superior mediastinal mass, who was ultimately diagnosed with a benign nodular goiter after undergoing EUS-FNA.8 In 2014, a case of primary papillary thyroid cancer was diagnosed via EUS-FNA after the authors initially noted a 1.7cm x 1.5cm hypoechoic lesion upon withdrawal of the echoendoscope during an evaluation for mediastinal adenopathy.9

EUS-FNA has also been used to diagnose a parathyroid adenoma in a case report detailing a patient who presented with pancreatitis as well as a mass extending from the right inferior aspect of the thyroid gland into the mediastinum. The diagnosis of parathyroid adenoma was confirmed from EUS-FNA biopsy and the patient subsequently underwent surgical resection.10

Head and Neck Infections

Case reports have also described EUS-FNA as a useful technique for diagnosing abscesses in the head and neck. One such report described a case of a soft tissue mass, approximately 5cm x 3cm, located between C7 and T1. Following EUS-FNA, the patient was diagnosed with a paraspinal abscess and underwent successful treatment with surgical drainage and debridement and long-term parenteral antibiotics.11 Similarly, parapharyngeal abscesses have also been drained using EUS via a transoral approach in place of the traditional ultrasound guided transcutaneous drainage.12

Lung Masses

Traditionally, tissue biopsy from the lung is acquired via bronchoscopy or endobronchial ultrasound (EBUS), usually performed by interventional pulmonologists, interventional radiologists or thoracic surgeons. EUS has been shown to provide tissue diagnosis in cases where bronchoscopy samples were non-diagnostic or where lesions were not within reach of a bronchoscope.13

The literature contains a relative paucity of studies regarding EUS-guided tissue acquisition from the lung, most likely due to concerns about inadvertently causing a pneumothorax. A study of 32 patients found a high diagnostic accuracy of EUS-FNA for establishing the diagnosis of lung cancer in 31 patients (97%) with periesophageal lung lesions.14 The authors reported no significant adverse events following EUS-FNA.13 Another study published in 2019, which included 19 patients, found a similar efficacy with diagnostic EUS-FNA in 100% of cases, without reported complications.15 In seven cases, EUS-FNA had the added advantage of obtaining tissue from distant metastatic sites (adrenal glands, mediastinal lymph nodes and liver metastasis), during the same session.14

A review of the literature yielded an additional 15 patients who underwent EUS-FNA for lung lesions and nodules as reported in case reports or as a subset of larger cohorts.16,17,18 Additionally, two cases of successful endoscopic ultrasound fine needle biopsy (EUS-FNB) of periesophageal, intraparenchymal, lung masses have been described, neither of which were associated with adverse events.19 (Figure 1) This last study suggests that intraparenchymal lesions can be biopsied without causing a pneumothorax, although the rate with which this adverse event arises in this setting remains unknown given the small number of patients treated in this manner to date.

Lastly, one case of pulmonary aspergillosis diagnosed by EUS-FNA has been reported. The authors describe 74-year-old patient with a history of acute myeloid leukemia who presented with febrile neutropenia as well as a 3cm x 2.2cm mass in the right upper lung on CT imaging. After EUS-FNA, microbiology ultimately proved positive for Aspergillus fumigatus.20 No post procedural complications were noted, including pneumothorax, and the patient improved after treatment with antifungals.19

Adrenal Glands

As mentioned above, EUS-FNA has been used to diagnose adrenal metastasis in primary lung cancers during the same session.14 Comparatively more evidence is available to document the utility of EUS-FNA with regards to identifying and sampling adrenal lesions. A recent meta-analysis documented the high diagnostic accuracy for EUSFNA for detection of adrenal gland lesions. The study included a total of 360 adrenal lesions, of which 137 were sampled and found to be positive for malignancy. Reported sensitivity and specificity of EUS-FNA for detecting metastatic adrenal gland lesions were 95% and 99%, respectively.21 Of the 25 articles included for meta-analysis, none reported adverse events associated with EUS-FNA for adrenal gland lesions.20 Similarly, a review article, which included 17 original articles and a total of 416 cases also found a low rate of adverse events with a single reported case of adrenal hemorrhage.22 Due to anatomical constraints, the majority of tissue acquisition was obtained from the left adrenal gland. However, in 40 cases from the studies mentioned above, the right adrenal was sampled successfully.20, 21 (Figure 2)

A recent national, multisite study of EUS guided tissue acquisition conducted in Spain found comparable results with regards to diagnostic yield and safety for EUS-FNA of the adrenal glands. The study included a total of 204 cases of tissue acquisition from the adrenal glands obtained in 200 patients. The authors found a diagnostic yield of 91.17%, inclusive of malignant plus benign diagnostic results, with no significant difference between FNA (n=153) or FNB (n=31). Fourteen of the reported cases were obtained from the right adrenal gland. The authors state that no serious adverse events occurred during the study. In two cases, patients were diagnosed with previously undiscovered pheochromocytomas. The patients did not have prior urine studies but did not suffer puncture associated hypertensive events. The authors concluded that urine studies may not be needed, especially in cases with known primary malignancy.23

Pelvic Masses

EUS guided biopsy can be used for a number of intrapelvic pathologies including: malignancy, cysts, abscesses and even endometriosis.24,25,26,27,28 (Figure 3) Several single-center retrospective studies exist in the literature documenting the diagnostic efficacy and safety of EUS guided tissue acquisition for pelvic masses.23,24,25 The largest of these studies included a total of 127 patients with pelvic lesions, of which 44 cases had surgical pathology available for comparision.25 The authors concluded that EUS-FNA of pelvic lesions to have a sensitivity of 89.3%, specificity of 100%, and a diagnostic accuracy of 93.2%.25 Of the cases included for analysis, 45% were positive for malignancy, 4.7% were considered suspicious/ atypical and 50.3% were negative for malignancy.25 Among malignant cases, adenocarcinoma was identified in 18%, undifferentiated carcinoma in 16%, squamous cell carcinoma in 4%, neuroendocrine tumor in 2%, urothelial carcinoma in 2%, gastrointestinal stromal tumor in 1% and non-Hodgkin lymphoma in 1%.25 No complications were noted during the study.

One study of 20 patients with pelvic lesions who underwent EUS-FNA found similar sensitivities and specificities (90% and 100%, respectively) when compared to available surgical pathology.24 No early or late complications were noted during this study.24 Another study included 29 patients with pelvic masses, of whom 17 had surgical pathology available for comparison, which found EUS-FNA to have a sensitivity of 88% and a specificity of 100%.23 The authors also included 5 cases where EUS-FNB was also performed, which had a lower sensitivity of 67% and a specificity of 100%.23 Two patients with cystic lesions developed abscesses after undergoing EUS-FNA, both of which required antibiotic treatment and percutaneous drainage.23

DISCUSSION

Since the initial case report of EUS guided FNA of a pancreatic head lesion in 1992,29 EUS guided tissue acquisition has expanded its utility to a broad range of clinical scenarios. EUS guided tissue acquisition can be used to biopsy virtually any target within close proximity of the gastrointestinal tract including disparate sites all over the mediastinum, abdomen and pelvis. This review has detailed some unusual or less commonly biopsied sites including: thyroid, parathyroid, head and neck masses, lung masses, adrenal glands and pelvic masses. Given the diversity of biopsy sites presented here, successful EUS guided tissue acquisition should involve a detailed understanding of individual patient anatomy and, when appropriate, interdisciplinary discussion with interventional radiology, as well as relevant medical and surgical specialties.30 As EUS guided FNA and FNB continue to be implemented in novel ways, additional research is needed for to further assess the safety profile and diagnostic accuracy of EUS guided tissue acquisition

References

  1. Cazacu IM, Luzuriaga Chavez AA, Saftoiu A, Vilmann P, Bhutani MS. A quarter century of EUS-FNA: Progress, milestones, and future directions. Endosc Ultrasound. 2018 May-Jun;7(3):141-160.
  2. Devereaux BM, Leblanc JK, Yousif E, Kesler K, Brooks J, Mathur P, Sandler A, Chappo J, Lehman GA, Sherman S, Gress F, Ciaccia D. Clinical utility of EUS-guided fineneedle aspiration of mediastinal masses in the absence of known pulmonary malignancy. Gastrointest Endosc. 2002 Sep;56(3):397-401.
  3. Eloubeidi MA, Khan AS, Luz LP, Linder A, Moreira DM, Crowe DR, Eltoum IA. Combined use of EUS-guided FNA and immunocytochemical stains discloses metastatic and unusual diseases in the evaluation of mediastinal lymphadenopathy of unknown etiology. Ann Thorac Med. 2012 Apr;7(2):84-91.
  4. Wildi SM, Fickling WE, Day TA, Cunningham CD 3rd, Schmulewitz N, Varadarajulu S, Roberts SS, Ferguson B, Hoffman BJ, Hawes RH, Wallace MB. Endoscopic ultrasonography in the diagnosis and staging of neoplasms of the head and neck. Endoscopy. 2004 Jul;36(7):624-30.
  5. Koike E, Yamashita H, Noguchi S, Ohshima A, Yamashita H, Watanabe S, Uchino S, Arita T, Kuroki S, Tanaka M. Endoscopic ultrasonography in patients with thyroid cancer: its usefulness and limitations for evaluating esophagopharyngeal invasion. Endoscopy. 2002 Jun;34(6):457-60.
  6. Alkhatib AA, Mahayni AA, Chawki GR, Yoder L, Elkhatib FA, Al-Haddad M. Endoscopic evaluation of thyroid gland among patients with nonthyroid cancers. Endosc Ultrasound. 2016 Sep-Oct;5(5):328-334.
  7. Sawhney MS, Nelson DB, Debol S. Gastrointest Endosc. The ever-expanding spectrum of GI endoscopy: EUSguided FNA of thyroid cancer. 2007 Feb;65(2):319-20; discussion 320. Epub 2006 Nov 1.
  8. Dewitt J, Youssef W, Leblanc J, McHenry L, McGreevy K, Chappo J, Cramer H, Sherman S. EUS-guided FNA of a thyroid mass. Gastrointest Endosc. 2004 Feb;59(2):307- 10.
  9. Jalil AA, Elkhatib FA, Mahayni AA, Alkhatib AA. Primary papillary thyroid carcinoma diagnosed using endoscopic ultrasound with fine needle aspiration. Clin Endosc. 2014 Jul;47(4):350-2.
  10. Balekuduru AB, Rao PS, Subbaraj SB. Endoscopic Ultrasound-guided Transesophageal Biopsy of Parathyroid Adenoma. J Dig Endosc. 2017;8:187-9.
  11. Clary K, Varadarajulu S, Canon C, Jhala N, Jhala DN. Diagnosis of paraspinal abscess by EUS-guided FNA. Gastrointest Endosc. 2007 Apr;65(4):729-31.
  12. Balekuduru AB, Dutta AK, Subbaraj SB. Endoscopic ultrasound-guided transoral drainage of parapharyngeal abscess. Digestive Endosc. 2016; 28: 755-759.
  13. Fickling W, Wallace MB. Gastrointest Endosc. EUS in lung cancer. 2002 Oct;56(4 Suppl):S18-21.
  14. Annema JT, Veseliç M, Rabe KF. EUS-guided FNA of centrally located lung tumours following a non-diagnostic bronchoscopy. Lung Cancer. 2005 Jun;48(3):357-61; discussion 363-4. Epub 2005 Jan 21.
  15. Chira RI, Chira A, Ichim VA, Nagy GA, Florea A, Crisan D, Popovici B. Endoscopic ultrasound-guided aspiration (EUS-FNA) of paraesophageal lung tmors – diagnostic yield and added value. Med Ultrason. 2019 Nov 24;21(4):377-381.
  16. Dincer HE, Gliksberg EP, Andrade RS. Endoscopic ultrasound and/or endobronchial ultrasound-guided needle biopsy of central intraparenchymal lung lesions not adjacent to airways or esophagus. Endosc Ultrasound. 2015 Jan-Mar;4(1):40-3.
  17. Bugalho A, Ferreira D, Eberhardt R, Dias SS, Videira PA, Herth FJ, Carreiro L. Diagnostic value of endobronchial and endoscopic ultrasound-guided fine needle aspiration for accessible lung cancer lesions after non-diagnostic conventional techniques: a prospective study. BMC Cancer. 2013 Mar 19;13:130.
  18. Lin LF, Huang PT, Tsai MH, Chen TM, Ho KS. Role of endoscopic ultrasound-guided fine-needle aspiration in lung and mediastinal lesions. J Chin Med Assoc. 2010 Oct;73(10):523-9.
  19. Adler DG, Gabr M, Taylor LJ, Witt B, Pleskow D. Initial report of transesophageal EUS-guided intraparenchymal lung mass core biopsy: Findings and outcome in two cases. Endosc Ultrasound. 2018 Nov-Dec;7(6):413-417.
  20. Rodrigues-Pinto E, Lopes S, Principe F, Costa J, Macedo G. Pulmonary aspergillosis diagnosed by endoscopic ultrasound fine-needle aspiration. Endosc Ultrasound. 2016 Jan-Feb;5(1):58-60.
  21. Patel S, Jinjuvadia R, Devara A, Naylor PH, Anees M, Jinjuvadia K, Al-Haddad M. Performance characteristics of EUS-FNA biopsy for adrenal lesions: a meta-analysis. Endosc Ultrasound. 2019 May-Jun;8(3):180-187.
  22. Rashmee Patil, Mel A. Ona, Charilaos Papafragkakis, Sushil Duddempudi, Sury Anand, Laith H. Jamil Endoscopic ultrasound-guided fine-needle aspiration in the diagnosis of adrenal lesions. Ann Gastroenterol. 2016 JulSep; 29(3): 307–311. Published online 2016 May 20.
  23. Martin-Cardona A, Fernandez-Esparrach G, Subtil JC, Iglesias-Garcia J, Garcia-Guix M, Barturen Barroso A, Gimeno-Garcia AZ, Esteban JM, Pardo Balteiro A, Velasco-Guardado A, Vazquez-Sequeiros E, Loras C, Martinez-Moreno B, Castellot A, Huertas C, MartinezLapiedra M, Sanchez-Yague A, Teran A, Morales-Alvarado VJ, Betes M, de la Iglesia D, Sánchez-Montes C, Lozano MD, Lariño-Noia J, Gines A, Tebe C, Gornals JB. EUSguided tissue acquisition in the study of the adrenal glands: results of a nationwide multicenter study. PLoS One. 2019 Jun 6;14(6):e0216658.
  24. Mohamadnejad M, Al-Haddad MA, Sherman S, McHenry L, Leblanc JK, DeWitt J. Utility of EUS-guided biopsy of extramural pelvic masses. Gastrointest Endosc. 2012 Jan;75(1):146-51.
  25. Rzouq F, Brown J, Fan F, Oropeza-Vail M, Sidorenko E, Gilroy R, Esfandyari T, Bonino J, Olyaee M. The utility of lower endoscopic ultrasound-guided fine needle aspiration for the diagnosis of benign and malignant pelvic diseases. J Clin Gastroenterol. 2014 Feb;48(2):127-30.
  26. Hassan GM, Paquin SC, Albadine R, Gariépy G, Soucy G, Nguyen BN, Sahai AV. Endoscopic-guided FNA of pelvic lesions: a large single-center experience. Cancer Cytopathol. 2016 Nov;124(11):836-841.
  27. Adler DG, Lanke G. Clinical Update on the Role of EUS in Pelvic Abscess. Practical Gastroenterology. 2020 Mar.
  28. Pishvaian AC, Ahlawat SK, Garvin D, Haddad NG. Role of EUS and EUS-guided FNA in the diagnosis of symptomatic rectosigmoid endometriosis. Gastrointest Endosc. 2006 Feb;63(2):331-5.
  29. Vilmann P, Jacobsen GK, Henriksen FW et al. Endoscopic ultrasonography with guided fine needle aspiration biopsy in pancreatic disease. Gastrointest Endosc. 1992;38:172-3.
  30. Fujii LL, Levy MJ.Basic techniques in endoscopic ultrasound-guided fine needle aspiration for solid lesions: adverse events and avoiding them. Endosc Ultrasound. 2014 Jan;3(1):35-45.

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A CASE REPORT

Incidental Pancreatic Neuroendocrine Neoplasm Diagnosed by Confocal Laser Endomicroscopy: A Case Report and Brief Literature Review

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While a majority of the pancreatic cystic lesions (PCL) are benign incidentalomas, many of them can be neoplastic and preneoplastic. Endoscopic ultrasound-guided fine needle aspiration is commonly utilized for the diagnosis of these lesions; however, the sensitivity and specificity are suboptimal. Confocal laser endomicroscopy (CLE) is a more reliable diagnostic tool that is being increasingly used for the diagnosis of PCL. Cystic neuroendocrine neoplasms (NEN) of the pancreas are thought to contribute to a very small proportion of all PCL. Nonetheless, they have been found more commonly in recent studies than previously reported. Here, we present a case report of a patient with cystic NEN in the pancreatic tail that was incidentally found, and CLE was used for diagnosis.

INTRODUCTION

With widespread use of abdominal imaging for diagnostic and screening purposes, the prevalence of pancreatic cystic lesions (PCL) has surged, ranging from less than 1% in an earlier study to 2.6% in a more recent report.1,2 Endoscopic ultrasound-guided fine needle aspiration (EUS-FNA) is utilized for the diagnosis of these lesions, however, the diagnostic yield is often limited by inadequate cells for analysis in the cystic fluid aspirated. Confocal laser endomicroscopy (CLE), also known as optical biopsy, is a technique that utilizes low frequency laser beam to obtain real-time pictures of the tissues that mimics histological images. While there is emerging evidence of the application of CLE in the diagnosis of mucinous PCL with sensitivity, specificity and accuracy of approximately 90%, there are only few reports of the use of CLE in the diagnosis of cystic neuroendocrine neoplasms (NEN) of the pancreas.3-5

Here, we present the case history of a patient with incidentally detected PCL who underwent CLE and was diagnosed to have a NEN of the pancreas.

Case Report

A 76-year-old male with past medical history of arthritis, diabetes type II, hypertension and neuropathy, presented to emergency department for evaluation of acute onset right flank pain and nausea, without vomiting. Physical exam revealed normal vital signs and positive findings included tenderness in the right costovertebral angle. There was no history of weight loss or fever. There was no history of tobacco, alcohol, or drug use. Family history was significant for multiple types of cancer in siblings, including skin, breast, pancreas, and bladder.

Computed tomography (CT) of the abdomen and pelvis revealed right nephrolithiasis with hydronephrosis, and an incidental finding of a lowdensity lesion in the tail of the pancreas measuring 1.7 x 2.1 x 2.3 cm3 (Figure 1). Magnetic resonance cholangiopancreatography (MRCP) showed a round rim-enhancing cyst along the pancreatic tail measuring 17 mm x 17 mm axially and 21 mm craniocaudally without definitive communication with the pancreatic duct (Figure 2). Lab results were unremarkable other than elevated serum lipase of 186 U/L and CA19-9 of 54.7 IU/ml.

Following treatment of his nephrolithiasis he was referred for an endoscopic ultrasound (EUS) for further evaluation of the pancreatic lesion.

EUS with CLE, FNA and Wall Biopsy

EUS showed normal main pancreatic duct and a 20.5 mm x 19.4 mm well circumscribed anechoic cystic lesion with atypical wall thickening in the tail of the pancreas without internal septations, solid component or mural nodules within the cyst. Under ultrasound guidance, a 19 g Boston Scientific needle was used for cyst puncture. This has been illustrated in Figure 1. Advanced imaging with CLE (Cellvizio) was performed. The wall of the cyst was surveyed and cluster of cells with trabecular pattern was seen consistent with NEN, as shown in Figure 2. Biopsy of the wall was performed with micro-forceps and the cyst was aspirated.

Pathology revealed neuroendocrine cell proliferation with cells positive for synaptophysin (Figure 3), chromogranin, and pancytokeratin by immunostains, Ki-67 proliferation was 1% and mitosis was not identified favoring welldifferentiated neuroendocrine tumor, WHO grade 1.

DISCUSSION

PCL are common and often asymptomatic with a majority discovered as incidental finding on imaging for other indications. They encompass pancreatic pseudocysts, intraductal papillary mucinous neoplasms, serous cystadenomas, and rarely cystic NEN. Imaging features are not characteristic of any cyst and in the absence of specific findings, like presence of a solid component or involvement of the main pancreatic duct, decision to defer further follow up or treatment cannot be made with confidence. Cystic NEN of pancreas account for less than 1% of all PCL (10-17% of NEN).6,7 The prevalence increases with age, the highest being in those 80 years and older (8.7%).1

Current guidelines recommend further evaluation and surveillance of PCL in medically fit patients other than asymptomatic pseudocysts and serous cystadenomas which have very low to no malignant potential. Given rarity of cystic NEN there is no clear guidance, and EUS-FNA is suggested. However, the yield of EUS-FNA is offset by low cellularity and nonspecific nature of the commonly used biomarkers, like carcinoembryonic antigen (CEA).8

CLE has developed as a real-time diagnostic tool for PCL. There is limited data on the utility of CLE in cystic NEN due to infrequent finding of these lesions. Nonetheless, the results from other cystic lesions can be extrapolated to these tumors. Our case report illustrates that not all PCL are benign and pancreatic NEN can present as an incidental cyst. The findings on CLE were characteristic of a cystic pancreatic NEN which was verified on histopathology.

CONCLUSION

Cystic NEN are uncommon, however, they are being recognized more frequently than before, and can present as an incidental cyst typically in the pancreatic body or tail. CLE can provide real-time diagnosis of PCL including cystic NEN. Current evidence for CLE in PCL is evolving and the initial results are encouraging. Future investigations of larger scale are expected to support this novel diagnostic modality as a standard of care.

References

  1. Laffan TA, Horton KM, Klein AP, et al. Prevalence of Unsuspected Pancreatic Cysts on MDCT. American Journal of Roentgenology. 2008/09/01 2008;191(3):802-807. doi:10.2214/AJR.07.3340
  2. Spinelli KS, Fromwiller TE, Daniel RA, et al. Cystic pancreatic neoplasms: observe or operate. Ann Surg. May 2004;239(5):651-7; discussion 657-9. doi:10.1097/01. sla.0000124299.57430.ce
  3. Krishna SG, Brugge WR, Dewitt JM, et al. Needle-based confocal laser endomicroscopy for the diagnosis of pancreatic cystic lesions: an international external interobserver and intraobserver study (with videos). Gastrointest Endosc. Oct 2017;86(4):644-654.e2. doi:10.1016/j.gie.2017.03.002
  4. Krishna SG, Swanson B, Hart PA, et al. Validation of diagnostic characteristics of needle based confocal laser endomicroscopy in differentiation of pancreatic cystic lesions. Endosc Int Open. Nov 2016;4(11):E1124-e1135. doi:10.1055/s-0042-116491
  5. Napoléon B, Lemaistre AI, Pujol B, et al. A novel approach to the diagnosis of pancreatic serous cystadenoma: needle-based confocal laser endomicroscopy. Endoscopy. Jan 2015;47(1):26-32. doi:10.1055/s-0034-1390693
  6. Ahrendt SA, Komorowski RA, Demeure MJ, Wilson SD, Pitt HA. Cystic pancreatic neuroendocrine tumors: is preoperative diagnosis possible? J Gastrointest Surg. Jan-Feb 2002;6(1):66-74. doi:10.1016/s1091-255x(01)00020-8
  7. Kawamoto S, Johnson PT, Shi C, et al. Pancreatic neuroendocrine tumor with cystlike changes: evaluation with MDCT. AJR Am J Roentgenol. 2013;200(3):W283-W290. doi:10.2214/AJR.12.8941
  8. Elta GH, Enestvedt BK, Sauer BG, Lennon AM. ACG Clinical Guideline: Diagnosis and Management of Pancreatic Cysts. Am J Gastroenterol. Apr 2018;113(4):464-479. doi:10.1038/ ajg.2018.14

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