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Plexiform Fibromyxoma: A Rare Gastric Tumor

Plexiform fibromyxoma is a rare and distinctive benign mesenchymal neoplasm that occurs in the gastric antrum. This tumor has a potential for misdiagnosis as gastrointestinal stromal tumor (GIST). It causes mucosa and vascular ulcerations without advancement of the tumor. Cytological bland spindle c...

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Detalles Bibliográficos
Autores principales: Wambura, Casmir, Surani, Salim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5727638/
https://www.ncbi.nlm.nih.gov/pubmed/29318062
http://dx.doi.org/10.1155/2017/4014565
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author Wambura, Casmir
Surani, Salim
author_facet Wambura, Casmir
Surani, Salim
author_sort Wambura, Casmir
collection PubMed
description Plexiform fibromyxoma is a rare and distinctive benign mesenchymal neoplasm that occurs in the gastric antrum. This tumor has a potential for misdiagnosis as gastrointestinal stromal tumor (GIST). It causes mucosa and vascular ulcerations without advancement of the tumor. Cytological bland spindle cells within a variably myxoid stroma characterize the histology of the tumor. We report the case of a 41-year-old African Tanzanian lady who presented with melena and recurrent anemia. Endoscopy and imaging studies revealed antral mass with initial suspicion of a GIST. However, immunohistochemically it turned to be a plexiform fibromyxoma. Follow-up evaluation 12 months after surgery revealed no evidence of recurrence or metastasis. This is a very uncommon tumor, which, to our knowledge, has been reported only once in Africa. The clinicians need to be aware of this rare occurrence to avoid misdiagnosis as GIST tumor.
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spelling pubmed-57276382018-01-09 Plexiform Fibromyxoma: A Rare Gastric Tumor Wambura, Casmir Surani, Salim Case Rep Gastrointest Med Case Report Plexiform fibromyxoma is a rare and distinctive benign mesenchymal neoplasm that occurs in the gastric antrum. This tumor has a potential for misdiagnosis as gastrointestinal stromal tumor (GIST). It causes mucosa and vascular ulcerations without advancement of the tumor. Cytological bland spindle cells within a variably myxoid stroma characterize the histology of the tumor. We report the case of a 41-year-old African Tanzanian lady who presented with melena and recurrent anemia. Endoscopy and imaging studies revealed antral mass with initial suspicion of a GIST. However, immunohistochemically it turned to be a plexiform fibromyxoma. Follow-up evaluation 12 months after surgery revealed no evidence of recurrence or metastasis. This is a very uncommon tumor, which, to our knowledge, has been reported only once in Africa. The clinicians need to be aware of this rare occurrence to avoid misdiagnosis as GIST tumor. Hindawi 2017 2017-11-26 /pmc/articles/PMC5727638/ /pubmed/29318062 http://dx.doi.org/10.1155/2017/4014565 Text en Copyright © 2017 Casmir Wambura and Salim Surani. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Wambura, Casmir
Surani, Salim
Plexiform Fibromyxoma: A Rare Gastric Tumor
title Plexiform Fibromyxoma: A Rare Gastric Tumor
title_full Plexiform Fibromyxoma: A Rare Gastric Tumor
title_fullStr Plexiform Fibromyxoma: A Rare Gastric Tumor
title_full_unstemmed Plexiform Fibromyxoma: A Rare Gastric Tumor
title_short Plexiform Fibromyxoma: A Rare Gastric Tumor
title_sort plexiform fibromyxoma: a rare gastric tumor
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5727638/
https://www.ncbi.nlm.nih.gov/pubmed/29318062
http://dx.doi.org/10.1155/2017/4014565
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AT suranisalim plexiformfibromyxomaararegastrictumor