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Non-familial juvenile polyposis of the stomach with gastric cancers: a case report

BACKGROUND: Juvenile polyposis is an autosomal dominant inherited disease characterized by the development of numerous hamartomatous and nonneoplastic polyps of the gastrointestinal tract. Juvenile polyposis has also recently been reported as a predisposition for gastrointestinal cancer. CASE PRESEN...

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Autores principales: Jogo, Tomoko, Oki, Eiji, Fujiwara, Minako, Kurashige, Junji, Nakanishi, Ryota, Sugiyama, Masahiko, Nakashima, Yuichiro, Saeki, Hiroshi, Tsuruta, Shinichi, Nishimura, Masataka, Oda, Yoshinao, Maehara, Yoshihiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6057863/
https://www.ncbi.nlm.nih.gov/pubmed/30043121
http://dx.doi.org/10.1186/s40792-018-0488-2
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author Jogo, Tomoko
Oki, Eiji
Fujiwara, Minako
Kurashige, Junji
Nakanishi, Ryota
Sugiyama, Masahiko
Nakashima, Yuichiro
Saeki, Hiroshi
Tsuruta, Shinichi
Nishimura, Masataka
Oda, Yoshinao
Maehara, Yoshihiko
author_facet Jogo, Tomoko
Oki, Eiji
Fujiwara, Minako
Kurashige, Junji
Nakanishi, Ryota
Sugiyama, Masahiko
Nakashima, Yuichiro
Saeki, Hiroshi
Tsuruta, Shinichi
Nishimura, Masataka
Oda, Yoshinao
Maehara, Yoshihiko
author_sort Jogo, Tomoko
collection PubMed
description BACKGROUND: Juvenile polyposis is an autosomal dominant inherited disease characterized by the development of numerous hamartomatous and nonneoplastic polyps of the gastrointestinal tract. Juvenile polyposis has also recently been reported as a predisposition for gastrointestinal cancer. CASE PRESENTATION: A 63-year-old man underwent esophagogastroduodenoscopy because of anemia and hypoalbuminemia during a follow-up for gastric polyposis, which showed multiple reddish polyps and two elevated lesions in the stomach. The elevated lesions were diagnosed as well-differentiated adenocarcinomas by biopsy. He had no specific physical findings or family history. Computed tomography showed gastric wall thickening without lymphadenopathy or distant metastasis. Colonoscopy showed an adenoma in the transverse colon. He underwent laparoscopy-assisted total gastrectomy with Roux-en-Y esophagojejunostomy. The resected specimen revealed numerous variously sized non-pedunculated polyps throughout the stomach, diagnosed histopathologically as hamartomatous polyps. The two elevated lesions were diagnosed as a well-differentiated adenocarcinoma restricted to the mucosa and a well-to-poorly differentiated adenocarcinoma invading the submucosa with prominent lymphatic permeation, respectively. Genetic analysis failed to identify any germline mutations in the genes usually associated with juvenile polyposis, including SMAD4 and BMPR1A. However, based on the few characteristic physical findings and histopathological features, the final diagnosis was juvenile polyposis restricted to the stomach. CONCLUSIONS: This patient represented a rare case of non-familial juvenile polyposis of the stomach with gastric cancers. Juvenile polyposis has malignant potential, and patients should therefore be carefully followed up. Surgical treatment, particularly total gastrectomy, is recommended as a standard treatment in patients with juvenile polyposis of the stomach with gastric cancer.
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spelling pubmed-60578632018-08-09 Non-familial juvenile polyposis of the stomach with gastric cancers: a case report Jogo, Tomoko Oki, Eiji Fujiwara, Minako Kurashige, Junji Nakanishi, Ryota Sugiyama, Masahiko Nakashima, Yuichiro Saeki, Hiroshi Tsuruta, Shinichi Nishimura, Masataka Oda, Yoshinao Maehara, Yoshihiko Surg Case Rep Case Report BACKGROUND: Juvenile polyposis is an autosomal dominant inherited disease characterized by the development of numerous hamartomatous and nonneoplastic polyps of the gastrointestinal tract. Juvenile polyposis has also recently been reported as a predisposition for gastrointestinal cancer. CASE PRESENTATION: A 63-year-old man underwent esophagogastroduodenoscopy because of anemia and hypoalbuminemia during a follow-up for gastric polyposis, which showed multiple reddish polyps and two elevated lesions in the stomach. The elevated lesions were diagnosed as well-differentiated adenocarcinomas by biopsy. He had no specific physical findings or family history. Computed tomography showed gastric wall thickening without lymphadenopathy or distant metastasis. Colonoscopy showed an adenoma in the transverse colon. He underwent laparoscopy-assisted total gastrectomy with Roux-en-Y esophagojejunostomy. The resected specimen revealed numerous variously sized non-pedunculated polyps throughout the stomach, diagnosed histopathologically as hamartomatous polyps. The two elevated lesions were diagnosed as a well-differentiated adenocarcinoma restricted to the mucosa and a well-to-poorly differentiated adenocarcinoma invading the submucosa with prominent lymphatic permeation, respectively. Genetic analysis failed to identify any germline mutations in the genes usually associated with juvenile polyposis, including SMAD4 and BMPR1A. However, based on the few characteristic physical findings and histopathological features, the final diagnosis was juvenile polyposis restricted to the stomach. CONCLUSIONS: This patient represented a rare case of non-familial juvenile polyposis of the stomach with gastric cancers. Juvenile polyposis has malignant potential, and patients should therefore be carefully followed up. Surgical treatment, particularly total gastrectomy, is recommended as a standard treatment in patients with juvenile polyposis of the stomach with gastric cancer. Springer Berlin Heidelberg 2018-07-24 /pmc/articles/PMC6057863/ /pubmed/30043121 http://dx.doi.org/10.1186/s40792-018-0488-2 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Case Report
Jogo, Tomoko
Oki, Eiji
Fujiwara, Minako
Kurashige, Junji
Nakanishi, Ryota
Sugiyama, Masahiko
Nakashima, Yuichiro
Saeki, Hiroshi
Tsuruta, Shinichi
Nishimura, Masataka
Oda, Yoshinao
Maehara, Yoshihiko
Non-familial juvenile polyposis of the stomach with gastric cancers: a case report
title Non-familial juvenile polyposis of the stomach with gastric cancers: a case report
title_full Non-familial juvenile polyposis of the stomach with gastric cancers: a case report
title_fullStr Non-familial juvenile polyposis of the stomach with gastric cancers: a case report
title_full_unstemmed Non-familial juvenile polyposis of the stomach with gastric cancers: a case report
title_short Non-familial juvenile polyposis of the stomach with gastric cancers: a case report
title_sort non-familial juvenile polyposis of the stomach with gastric cancers: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6057863/
https://www.ncbi.nlm.nih.gov/pubmed/30043121
http://dx.doi.org/10.1186/s40792-018-0488-2
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