Literature DB >> 21960285

Endoscopic management of duodenal adenomas in familial adenomatous polyposis--a single-center experience.

Sathya Jaganmohan1, Patrick M Lynch, Ramu P Raju, William A Ross, Jeffrey E Lee, Gottumukkala S Raju, Manoop S Bhutani, Jason B Fleming, Jeffrey H Lee.   

Abstract

BACKGROUND: Duodenal lesions (DLS) are common in patients with familial adenomatosis polyposis (FAP), and screening for duodenal adenocarcinoma (DA) is currently recommended. Endoscopic treatment of DLS is controversial. AIM: To report management and outcomes of endoscopic therapy for DLS in patients with FAP.
METHODS: The records of patients with FAP who underwent endoscopic surveillance or therapy for DLS over a 15-year period were reviewed. Endoscopic intervention included endoscopic surveillance with biopsies, argon plasma coagulation (APC), endoscopic mucosal resection (EMR), EMR with APC, and ampullectomy. Main outcome measurements were recurrence and histology of DLS after endoscopic therapy, complications of endoscopic therapy, and need for duodenectomy.
RESULTS: Seventy-one patients with FAP and DLS were identified from our endoscopy database as undergoing upper endoscopy for screening and/or surveillance (1995-2009). Mean follow up was 4.5 years (1-15 years). Seventy of the seventy-one (98.5%) patients had multiple flat DLS. Most of the patients were followed with yearly biopsies. APC was performed in 17 patients and EMR was performed in eight patients; in five of the eight EMR patients, APC was also performed to treat the edges of EMR site. During the follow up, 17/55 (31%) patients had histological progression (HP). HP was seen in 5/16 (31%) patients who underwent APC (one was lost to follow-up) and 12/40 (30%) patients followed with biopsies alone. Recurrence of lesions was noted in all patients. Two patients underwent duodenectomy. None of the patients developed DA during follow up.
CONCLUSIONS: Endoscopic surveillance with directed endotherapy for DLS in FAP is feasible and safe when diligently performed.

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Year:  2011        PMID: 21960285     DOI: 10.1007/s10620-011-1917-2

Source DB:  PubMed          Journal:  Dig Dis Sci        ISSN: 0163-2116            Impact factor:   3.199


  22 in total

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Review 2.  The role of endoscopy in ampullary and duodenal adenomas.

Authors:  Douglas G Adler; Waqar Qureshi; Raquel Davila; S Ian Gan; David Lichtenstein; Elizabeth Rajan; Bo Shen; Marc J Zuckerman; Robert D Fanelli; Trina Van Guilder; Todd H Baron
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3.  Immunohistochemical characteristics of duodenal adenomas in familial adenomatous polyposis with special reference to cell kinetics.

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4.  Randomized, placebo-controlled trial of gastric acid-lowering therapy on duodenal polyposis and relative adduct labeling in familial adenomatous polyposis.

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5.  Periampullary adenomas and adenocarcinomas in familial adenomatous polyposis: cumulative risks and APC gene mutations.

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6.  Randomized controlled trial of the effect of sulindac on duodenal and rectal polyposis and cell proliferation in patients with familial adenomatous polyposis.

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9.  Safety and outcome of endoscopic snare excision of the major duodenal papilla.

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10.  Photodynamic therapy for polyps in familial adenomatous polyposis--a pilot study.

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  12 in total

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Review 2.  Hereditary Colorectal Polyposis and Cancer Syndromes: A Primer on Diagnosis and Management.

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3.  Prospective study of acute complication rates and associated risk factors in endoscopic therapy for duodenal adenomas.

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4.  Rare combination of familial adenomatous polyposis and gallbladder polyps.

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5.  Role of endoscopy in patients with familial adenomatous polyposis.

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Review 6.  Duodenal adenocarcinoma: Advances in diagnosis and surgical management.

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Review 7.  Duodenal adenoma surveillance in patients with familial adenomatous polyposis.

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Review 9.  Endoscopic management of duodenal adenomatosis in familial adenomatous polyposis-A case-based review.

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10.  Risk factors for advanced duodenal and ampullary adenomatosis in familial adenomatous polyposis: a prospective, single-center study.

Authors:  M Sulbaran; F G Campos; U Ribeiro; H S Kishi; P Sakai; E G H de Moura; L Bustamante-López; M Tomitão; S C Nahas; I Cecconello; A V Safatle-Ribeiro
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