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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Detalles Bibliográficos
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
Descripción
Sumario: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.
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