Case of an Inflammatory Myofibroblastic Tumor of the Duodenum / 대한소화기학회지
The Korean Journal of Gastroenterology
;
: 28-32, 2018.
Artigo
em Coreano
| WPRIM
| ID: wpr-715642
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.
Texto completo:
DisponíveL
Índice:
WPRIM (Pacífico Ocidental)
Assunto principal:
Órbita
/
Pleura
/
Recidiva
/
Estômago
/
Seguimentos
/
Doenças Raras
/
Tumores do Estroma Gastrointestinal
/
Diagnóstico
/
Duodeno
/
Miofibroblastos
Tipo de estudo:
Estudo diagnóstico
/
Estudo observacional
/
Estudo prognóstico
Limite:
Humanos
/
Masculino
Idioma:
Coreano
Revista:
The Korean Journal of Gastroenterology
Ano de publicação:
2018
Tipo de documento:
Artigo
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