Antral plexiform fibromyxoma: case report of a rare mesenchymal neoplasm

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Plexiform fibromyxoma (PF) is a rare mesenchymal neoplasm of the stomach usually arising in the gastric antrum, and its main differential diagnosis is gastrointestinal stromal tumor. Most common symptoms are hematemesis, anemia. Immunohistochemically, positivity for smooth muscle actin (SMA) and vim...

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Autores: Oliveira dos Santos, Carlos Eduardo, Malaman, Daniele, Arciniegas Sanmartin, Ivan David, Aleixo, Pedro, Lopes, Cesar Vivian, Pereira-Lima, Júlio Carlos
Formato: artículo
Fecha de Publicación:2023
Institución:Sociedad de Gastroenterología del Perú
Repositorio:Revista de Gastroenterología del Perú
Lenguaje:inglés
OAI Identifier:oai:ojs.revistagastroperu.com:article/1626
Enlace del recurso:https://revistagastroperu.com/index.php/rgp/article/view/1626
Nivel de acceso:acceso abierto
Materia:Fibromyxoma
Gastrointestinal stromal tumors
Gastrointestinal neoplasms
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spelling Antral plexiform fibromyxoma: case report of a rare mesenchymal neoplasmAntral plexiform fibromyxoma: case report of a rare mesenchymal neoplasmOliveira dos Santos, Carlos EduardoMalaman, DanieleArciniegas Sanmartin, Ivan DavidAleixo, PedroLopes, Cesar VivianPereira-Lima, Júlio CarlosFibromyxomaGastrointestinal stromal tumorsGastrointestinal neoplasmsFibromyxomaGastrointestinal stromal tumorsGastrointestinal neoplasms Plexiform fibromyxoma (PF) is a rare mesenchymal neoplasm of the stomach usually arising in the gastric antrum, and its main differential diagnosis is gastrointestinal stromal tumor. Most common symptoms are hematemesis, anemia. Immunohistochemically, positivity for smooth muscle actin (SMA) and vimentin suggests the diagnosis of PF. We report the case of a 56-year-old female patient with a 30- day history of nausea at presentation 4 years ago. Gastroscopy at that time revealed a subepithelial lesion (SEL) in the gastric antrum, measuring approximately 20 mm in diameter, with leakage of serous fluid after biopsy. Histopathology showed only an inflammatory process. Follow-up gastroscopies were performed 24, 36, and 48 months later, with surveillance biopsy at each follow-up. The last gastroscopies showed changes in lesion appearance, reduction in size, and absence of fluid leakage. Histopathology showed bland spindle cell proliferation, with a vaguely plexiform/multinodular pattern, in a fibromyxoid stroma with an arborizing capillary network without mitoses. The tumor cells were positive for SMA and negative for DOG1, CD117, CD34, S100, desmin, EMA, CD10, calponin, and beta-catenin. The choice of treatment and follow-up depends on the SEL features, but because no cases of malignancy or metastatic disease have previously been reported, the patient chose a conservative approach. Plexiform fibromyxoma (PF) is a rare mesenchymal neoplasm of the stomach usually arising in the gastric antrum, and its main differential diagnosis is gastrointestinal stromal tumor. Most common symptoms are hematemesis, anemia. Immunohistochemically, positivity for smooth muscle actin (SMA) and vimentin suggests the diagnosis of PF. We report the case of a 56-year-old female patient with a 30- day history of nausea at presentation 4 years ago. Gastroscopy at that time revealed a subepithelial lesion (SEL) in the gastric antrum, measuring approximately 20 mm in diameter, with leakage of serous fluid after biopsy. Histopathology showed only an inflammatory process. Follow-up gastroscopies were performed 24, 36, and 48 months later, with surveillance biopsy at each follow-up. The last gastroscopies showed changes in lesion appearance, reduction in size, and absence of fluid leakage. Histopathology showed bland spindle cell proliferation, with a vaguely plexiform/multinodular pattern, in a fibromyxoid stroma with an arborizing capillary network without mitoses. The tumor cells were positive for SMA and negative for DOG1, CD117, CD34, S100, desmin, EMA, CD10, calponin, and beta-catenin. The choice of treatment and follow-up depends on the SEL features, but because no cases of malignancy or metastatic disease have previously been reported, the patient chose a conservative approach. Sociedad de Gastroenterología del Perú2023-12-21info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://revistagastroperu.com/index.php/rgp/article/view/1626Revista de Gastroenterología del Perú; Vol. 43 No. 4 (2023); 364-367Revista de Gastroenterología del Perú; Vol. 43 Núm. 4 (2023); 364-3671609-722X1022-5129reponame:Revista de Gastroenterología del Perúinstname:Sociedad de Gastroenterología del Perúinstacron:SOCIOGASTROenghttps://revistagastroperu.com/index.php/rgp/article/view/1626/1217Derechos de autor 2023 Carlos Eduardo Oliveira dos Santos, Daniele Malaman, Ivan David Arciniegas Sanmartin, Pedro Aleixo, Cesar Vivian Lopes, Júlio Carlos Pereira-Limahttps://creativecommons.org/licenses/by/4.0info:eu-repo/semantics/openAccessoai:ojs.revistagastroperu.com:article/16262023-12-24T13:08:26Z
dc.title.none.fl_str_mv Antral plexiform fibromyxoma: case report of a rare mesenchymal neoplasm
Antral plexiform fibromyxoma: case report of a rare mesenchymal neoplasm
title Antral plexiform fibromyxoma: case report of a rare mesenchymal neoplasm
spellingShingle Antral plexiform fibromyxoma: case report of a rare mesenchymal neoplasm
Oliveira dos Santos, Carlos Eduardo
Fibromyxoma
Gastrointestinal stromal tumors
Gastrointestinal neoplasms
Fibromyxoma
Gastrointestinal stromal tumors
Gastrointestinal neoplasms
title_short Antral plexiform fibromyxoma: case report of a rare mesenchymal neoplasm
title_full Antral plexiform fibromyxoma: case report of a rare mesenchymal neoplasm
title_fullStr Antral plexiform fibromyxoma: case report of a rare mesenchymal neoplasm
title_full_unstemmed Antral plexiform fibromyxoma: case report of a rare mesenchymal neoplasm
title_sort Antral plexiform fibromyxoma: case report of a rare mesenchymal neoplasm
dc.creator.none.fl_str_mv Oliveira dos Santos, Carlos Eduardo
Malaman, Daniele
Arciniegas Sanmartin, Ivan David
Aleixo, Pedro
Lopes, Cesar Vivian
Pereira-Lima, Júlio Carlos
author Oliveira dos Santos, Carlos Eduardo
author_facet Oliveira dos Santos, Carlos Eduardo
Malaman, Daniele
Arciniegas Sanmartin, Ivan David
Aleixo, Pedro
Lopes, Cesar Vivian
Pereira-Lima, Júlio Carlos
author_role author
author2 Malaman, Daniele
Arciniegas Sanmartin, Ivan David
Aleixo, Pedro
Lopes, Cesar Vivian
Pereira-Lima, Júlio Carlos
author2_role author
author
author
author
author
dc.subject.none.fl_str_mv Fibromyxoma
Gastrointestinal stromal tumors
Gastrointestinal neoplasms
Fibromyxoma
Gastrointestinal stromal tumors
Gastrointestinal neoplasms
topic Fibromyxoma
Gastrointestinal stromal tumors
Gastrointestinal neoplasms
Fibromyxoma
Gastrointestinal stromal tumors
Gastrointestinal neoplasms
description Plexiform fibromyxoma (PF) is a rare mesenchymal neoplasm of the stomach usually arising in the gastric antrum, and its main differential diagnosis is gastrointestinal stromal tumor. Most common symptoms are hematemesis, anemia. Immunohistochemically, positivity for smooth muscle actin (SMA) and vimentin suggests the diagnosis of PF. We report the case of a 56-year-old female patient with a 30- day history of nausea at presentation 4 years ago. Gastroscopy at that time revealed a subepithelial lesion (SEL) in the gastric antrum, measuring approximately 20 mm in diameter, with leakage of serous fluid after biopsy. Histopathology showed only an inflammatory process. Follow-up gastroscopies were performed 24, 36, and 48 months later, with surveillance biopsy at each follow-up. The last gastroscopies showed changes in lesion appearance, reduction in size, and absence of fluid leakage. Histopathology showed bland spindle cell proliferation, with a vaguely plexiform/multinodular pattern, in a fibromyxoid stroma with an arborizing capillary network without mitoses. The tumor cells were positive for SMA and negative for DOG1, CD117, CD34, S100, desmin, EMA, CD10, calponin, and beta-catenin. The choice of treatment and follow-up depends on the SEL features, but because no cases of malignancy or metastatic disease have previously been reported, the patient chose a conservative approach.
publishDate 2023
dc.date.none.fl_str_mv 2023-12-21
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.none.fl_str_mv https://revistagastroperu.com/index.php/rgp/article/view/1626
url https://revistagastroperu.com/index.php/rgp/article/view/1626
dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv https://revistagastroperu.com/index.php/rgp/article/view/1626/1217
dc.rights.none.fl_str_mv https://creativecommons.org/licenses/by/4.0
info:eu-repo/semantics/openAccess
rights_invalid_str_mv https://creativecommons.org/licenses/by/4.0
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Sociedad de Gastroenterología del Perú
publisher.none.fl_str_mv Sociedad de Gastroenterología del Perú
dc.source.none.fl_str_mv Revista de Gastroenterología del Perú; Vol. 43 No. 4 (2023); 364-367
Revista de Gastroenterología del Perú; Vol. 43 Núm. 4 (2023); 364-367
1609-722X
1022-5129
reponame:Revista de Gastroenterología del Perú
instname:Sociedad de Gastroenterología del Perú
instacron:SOCIOGASTRO
instname_str Sociedad de Gastroenterología del Perú
instacron_str SOCIOGASTRO
institution SOCIOGASTRO
reponame_str Revista de Gastroenterología del Perú
collection Revista de Gastroenterología del Perú
repository.name.fl_str_mv
repository.mail.fl_str_mv
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