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IgG4-related Disease in the Stomach which Was Confused with Gastrointestinal Stromal Tumor (GIST): Two Case Reports and Review of the Literature
Journal of Gastric Cancer ; : 99-107, 2018.
Article en En | WPRIM | ID: wpr-713653
Biblioteca responsable: WPRO
ABSTRACT
Immunoglobulin G4-related disease (IgG4-RD) is an immune-mediated fibro-inflammatory disorder characterized by specific pathological findings and elevated serum IgG4 level. IgG4-RD in the stomach is rare, and occasionally diagnosed as gastric subepithelial tumor (SET) by endoscopy or computed tomography scan. Two female patients in the age group of 40–50 years were diagnosed with 4 cm sized gastric SET. One underwent laparoscopic gastric wedge resection. Another one had a history of subtotal gastrectomy for early gastric cancer and idiopathic thrombocytopenic purpura with oral steroids administration. She underwent a completion total gastrectomy with splenectomy for the gastric SET and ITP. The pathology showed storiform fibrosis, and IgG4 was positive in immunohistochemistry (IHC) stain. IgG4-RD is known as a medical disease that could be treated with oral steroids. The difficulty in preoperative diagnosis of the disease occasionally causes unnecessary gastric resection. Thus, preoperative diagnostic methods for IgG4-RD such as deep biopsy with IHC stain or magnetic resonance imaging are needed.
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Texto completo: 1 Índice: WPRIM Asunto principal: Patología / Esplenectomía / Esteroides / Estómago / Neoplasias Gástricas / Biopsia / Fibrosis / Inmunoglobulina G / Inmunoglobulinas / Inmunohistoquímica Tipo de estudio: Diagnostic_studies Límite: Female / Humans Idioma: En Revista: Journal of Gastric Cancer Año: 2018 Tipo del documento: Article
Texto completo: 1 Índice: WPRIM Asunto principal: Patología / Esplenectomía / Esteroides / Estómago / Neoplasias Gástricas / Biopsia / Fibrosis / Inmunoglobulina G / Inmunoglobulinas / Inmunohistoquímica Tipo de estudio: Diagnostic_studies Límite: Female / Humans Idioma: En Revista: Journal of Gastric Cancer Año: 2018 Tipo del documento: Article