Case of an Inflammatory Myofibroblastic Tumor of the Duodenum / 대한소화기학회지
The Korean Journal of Gastroenterology
; : 28-32, 2018.
Article
在 Ko
| WPRIM
| ID: wpr-715642
Responsible library:
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.
Key words
全文:
1
索引:
WPRIM
主要主题:
Orbit
/
Pleura
/
Recurrence
/
Stomach
/
Follow-Up Studies
/
Rare Diseases
/
Gastrointestinal Stromal Tumors
/
Diagnosis
/
Duodenum
/
Myofibroblasts
研究类型:
Diagnostic_studies
/
Observational_studies
/
Prognostic_studies
限制:
Humans
/
Male
语言:
Ko
期刊:
The Korean Journal of Gastroenterology
年:
2018
类型:
Article