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Gastric Glomus Tumor

This case report describes glomus tumor of the stomach, a rare entity, which is a mesenchymal origin tumor. They are generally benign and account for nearly 1% of all gastrointestinal (GI) soft-tissue tumors. They are almost impossible to diagnose preoperatively because of the lack of specific chara...

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Autores principales: Singh, Sumitoj, Kumar, Ashok, Singh, Vikas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7659754/
https://www.ncbi.nlm.nih.gov/pubmed/33223817
http://dx.doi.org/10.4103/njs.NJS_8_19
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author Singh, Sumitoj
Kumar, Ashok
Singh, Vikas
author_facet Singh, Sumitoj
Kumar, Ashok
Singh, Vikas
author_sort Singh, Sumitoj
collection PubMed
description This case report describes glomus tumor of the stomach, a rare entity, which is a mesenchymal origin tumor. They are generally benign and account for nearly 1% of all gastrointestinal (GI) soft-tissue tumors. They are almost impossible to diagnose preoperatively because of the lack of specific characteristics and are often mistaken for GI stromal tumors (GISTs). In our hospital setup, a female aged 24 years, presented with right lumbar abdominal pain which after a thorough workup leads to the preoperative diagnosis of GIST, and distal gastrectomy with Roux-en-y anastomosis was done. However, pathological and immunohistochemical findings done after the surgery were found consistent with the diagnosis of gastric glomus tumor. Discovered on GIST-1 (DOG-1) nonreactivity is considered for the diagnosis of glomus tumor which helps in excluding the diagnosis of GIST, which is positive for DOG-1. Hence, it was concluded that differential diagnosis on the basis of immunohistochemical findings can lead to an accurate preoperative diagnosis and further targeted surgical intervention.
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spelling pubmed-76597542020-11-19 Gastric Glomus Tumor Singh, Sumitoj Kumar, Ashok Singh, Vikas Niger J Surg Case Report This case report describes glomus tumor of the stomach, a rare entity, which is a mesenchymal origin tumor. They are generally benign and account for nearly 1% of all gastrointestinal (GI) soft-tissue tumors. They are almost impossible to diagnose preoperatively because of the lack of specific characteristics and are often mistaken for GI stromal tumors (GISTs). In our hospital setup, a female aged 24 years, presented with right lumbar abdominal pain which after a thorough workup leads to the preoperative diagnosis of GIST, and distal gastrectomy with Roux-en-y anastomosis was done. However, pathological and immunohistochemical findings done after the surgery were found consistent with the diagnosis of gastric glomus tumor. Discovered on GIST-1 (DOG-1) nonreactivity is considered for the diagnosis of glomus tumor which helps in excluding the diagnosis of GIST, which is positive for DOG-1. Hence, it was concluded that differential diagnosis on the basis of immunohistochemical findings can lead to an accurate preoperative diagnosis and further targeted surgical intervention. Wolters Kluwer - Medknow 2020 2020-07-27 /pmc/articles/PMC7659754/ /pubmed/33223817 http://dx.doi.org/10.4103/njs.NJS_8_19 Text en Copyright: © 2020 Nigerian Journal of Surgery http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Case Report
Singh, Sumitoj
Kumar, Ashok
Singh, Vikas
Gastric Glomus Tumor
title Gastric Glomus Tumor
title_full Gastric Glomus Tumor
title_fullStr Gastric Glomus Tumor
title_full_unstemmed Gastric Glomus Tumor
title_short Gastric Glomus Tumor
title_sort gastric glomus tumor
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7659754/
https://www.ncbi.nlm.nih.gov/pubmed/33223817
http://dx.doi.org/10.4103/njs.NJS_8_19
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