Nodular Lymphoid Hyperplasia in a Patient Initially Believed to Have Familial Adenomatous Polyposis

A 50-year-old male was initially thought to have familial adenomatous polyposis (FAP) after innumerable small nodules in the upper GI tract were discovered upon endoscopic retrograde cholangiopancreatography for common bile duct stone extraction. ERCP was unsuccessful due to inability to find the ma...

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Detalles Bibliográficos
Autores principales: Altafi, Soheil, Volfson, Ariy, McKinley, Matthew J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American College of Gastroenterology 2014
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4435284/
https://www.ncbi.nlm.nih.gov/pubmed/26157834
http://dx.doi.org/10.14309/crj.2014.10
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author Altafi, Soheil
Volfson, Ariy
McKinley, Matthew J.
author_facet Altafi, Soheil
Volfson, Ariy
McKinley, Matthew J.
author_sort Altafi, Soheil
collection PubMed
description A 50-year-old male was initially thought to have familial adenomatous polyposis (FAP) after innumerable small nodules in the upper GI tract were discovered upon endoscopic retrograde cholangiopancreatography for common bile duct stone extraction. ERCP was unsuccessful due to inability to find the major papilla amongst the nodules found in the duodenum. Biopsy of the nodules was consistent with nodular lymphoid hyperplasia. The patient was later found to have common variable immunodeficiency.
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spelling pubmed-44352842015-07-08 Nodular Lymphoid Hyperplasia in a Patient Initially Believed to Have Familial Adenomatous Polyposis Altafi, Soheil Volfson, Ariy McKinley, Matthew J. ACG Case Rep J Case Report A 50-year-old male was initially thought to have familial adenomatous polyposis (FAP) after innumerable small nodules in the upper GI tract were discovered upon endoscopic retrograde cholangiopancreatography for common bile duct stone extraction. ERCP was unsuccessful due to inability to find the major papilla amongst the nodules found in the duodenum. Biopsy of the nodules was consistent with nodular lymphoid hyperplasia. The patient was later found to have common variable immunodeficiency. American College of Gastroenterology 2014-01-10 /pmc/articles/PMC4435284/ /pubmed/26157834 http://dx.doi.org/10.14309/crj.2014.10 Text en Copyright © Altafi et al. This is an open-access article. This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/4.0/
spellingShingle Case Report
Altafi, Soheil
Volfson, Ariy
McKinley, Matthew J.
Nodular Lymphoid Hyperplasia in a Patient Initially Believed to Have Familial Adenomatous Polyposis
title Nodular Lymphoid Hyperplasia in a Patient Initially Believed to Have Familial Adenomatous Polyposis
title_full Nodular Lymphoid Hyperplasia in a Patient Initially Believed to Have Familial Adenomatous Polyposis
title_fullStr Nodular Lymphoid Hyperplasia in a Patient Initially Believed to Have Familial Adenomatous Polyposis
title_full_unstemmed Nodular Lymphoid Hyperplasia in a Patient Initially Believed to Have Familial Adenomatous Polyposis
title_short Nodular Lymphoid Hyperplasia in a Patient Initially Believed to Have Familial Adenomatous Polyposis
title_sort nodular lymphoid hyperplasia in a patient initially believed to have familial adenomatous polyposis
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4435284/
https://www.ncbi.nlm.nih.gov/pubmed/26157834
http://dx.doi.org/10.14309/crj.2014.10
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AT mckinleymatthewj nodularlymphoidhyperplasiainapatientinitiallybelievedtohavefamilialadenomatouspolyposis

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