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Megaduodenum associated with gastric strongyloidiasis

Gastric strongyloidiasis and megaduodenum are rare diseases. Gastrointestinal (GI) strongyloidiasis has many clinical features. One of them is megaduodenum. We describe a case of a 32-years-old man who has come to us from an endemic area for Strongyloides stercoralis. He had had megaduodenum diagnos...

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Autores principales: da Silva, Amanda Pinter Carvalheiro, Boteon, Yuri Longatto, Tercioti, Valdir, Lopes, Luiz Roberto, de Souza Coelho Neto, João, Andreollo, Nelson Adami
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4446660/
https://www.ncbi.nlm.nih.gov/pubmed/25951613
http://dx.doi.org/10.1016/j.ijscr.2014.11.066
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author da Silva, Amanda Pinter Carvalheiro
Boteon, Yuri Longatto
Tercioti, Valdir
Lopes, Luiz Roberto
de Souza Coelho Neto, João
Andreollo, Nelson Adami
author_facet da Silva, Amanda Pinter Carvalheiro
Boteon, Yuri Longatto
Tercioti, Valdir
Lopes, Luiz Roberto
de Souza Coelho Neto, João
Andreollo, Nelson Adami
author_sort da Silva, Amanda Pinter Carvalheiro
collection PubMed
description Gastric strongyloidiasis and megaduodenum are rare diseases. Gastrointestinal (GI) strongyloidiasis has many clinical features. One of them is megaduodenum. We describe a case of a 32-years-old man who has come to us from an endemic area for Strongyloides stercoralis. He had had megaduodenum diagnosed in his childhood. We submitted him to two surgeries. He has recovered just after the second surgery, a Roux-en-Y partial gastrectomy. After that, his follow-up was uneventful and the patient has gained 10 kg in weight. Histopathology confirmed gastric strongyloidiasis. In conclusion, if patients arrive from an endemic area of S. stercoralis and if they present GI symptoms or a previous diagnosis of megaduodenum, they must be considered for a histological evaluation for gastric strongyloidiasis.
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spelling pubmed-44466602015-05-29 Megaduodenum associated with gastric strongyloidiasis da Silva, Amanda Pinter Carvalheiro Boteon, Yuri Longatto Tercioti, Valdir Lopes, Luiz Roberto de Souza Coelho Neto, João Andreollo, Nelson Adami Int J Surg Case Rep Article Gastric strongyloidiasis and megaduodenum are rare diseases. Gastrointestinal (GI) strongyloidiasis has many clinical features. One of them is megaduodenum. We describe a case of a 32-years-old man who has come to us from an endemic area for Strongyloides stercoralis. He had had megaduodenum diagnosed in his childhood. We submitted him to two surgeries. He has recovered just after the second surgery, a Roux-en-Y partial gastrectomy. After that, his follow-up was uneventful and the patient has gained 10 kg in weight. Histopathology confirmed gastric strongyloidiasis. In conclusion, if patients arrive from an endemic area of S. stercoralis and if they present GI symptoms or a previous diagnosis of megaduodenum, they must be considered for a histological evaluation for gastric strongyloidiasis. Elsevier 2014-11-28 /pmc/articles/PMC4446660/ /pubmed/25951613 http://dx.doi.org/10.1016/j.ijscr.2014.11.066 Text en © 2014 The Authors http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/3.0/).
spellingShingle Article
da Silva, Amanda Pinter Carvalheiro
Boteon, Yuri Longatto
Tercioti, Valdir
Lopes, Luiz Roberto
de Souza Coelho Neto, João
Andreollo, Nelson Adami
Megaduodenum associated with gastric strongyloidiasis
title Megaduodenum associated with gastric strongyloidiasis
title_full Megaduodenum associated with gastric strongyloidiasis
title_fullStr Megaduodenum associated with gastric strongyloidiasis
title_full_unstemmed Megaduodenum associated with gastric strongyloidiasis
title_short Megaduodenum associated with gastric strongyloidiasis
title_sort megaduodenum associated with gastric strongyloidiasis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4446660/
https://www.ncbi.nlm.nih.gov/pubmed/25951613
http://dx.doi.org/10.1016/j.ijscr.2014.11.066
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