Case of an Inflammatory Myofibroblastic Tumor of the Duodenum / 대한소화기학회지
The Korean Journal of Gastroenterology
; : 28-32, 2018.
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.
Palavras-chave
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