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Case of an Inflammatory Myofibroblastic Tumor of the Duodenum / 대한소화기학회지
Article em Ko | WPRIM | ID: wpr-715642
Biblioteca responsável: WPRO
ABSTRACT
An inflammatory myofibroblastic tumor (IMT) is a rare disease that can occur in a variety of locations, including the lung, orbit, parotid, pleura, and stomach. Despite multiple reports in various organs, a duodenal IMT is rare with limited case reports. We encountered a case of a 49-year-old male with a duodenal IMT. The patient underwent a laparoscopic wedge resection under the impression of a duodenal mesenchymal tumor, such as gastrointestinal stromal tumor, but the final diagnosis was a duodenal IMT. The patient was treated successfully with an oral nonsteroidal anti-inflammatory drug for the residual lesions. He was free of recurrence during the 12 month follow-up period.
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Texto completo: 1 Índice: WPRIM Assunto principal: Órbita / Pleura / Recidiva / Estômago / Seguimentos / Doenças Raras / Tumores do Estroma Gastrointestinal / Diagnóstico / Duodeno / Miofibroblastos Tipo de estudo: Diagnostic_studies / Observational_studies / Prognostic_studies Limite: Humans / Male Idioma: Ko Revista: The Korean Journal of Gastroenterology Ano de publicação: 2018 Tipo de documento: Article
Texto completo: 1 Índice: WPRIM Assunto principal: Órbita / Pleura / Recidiva / Estômago / Seguimentos / Doenças Raras / Tumores do Estroma Gastrointestinal / Diagnóstico / Duodeno / Miofibroblastos Tipo de estudo: Diagnostic_studies / Observational_studies / Prognostic_studies Limite: Humans / Male Idioma: Ko Revista: The Korean Journal of Gastroenterology Ano de publicação: 2018 Tipo de documento: Article