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[Case of an Inflammatory Myofibroblastic Tumor of the Duodenum].

Authors :
Park SG
Kim GH
Park HJ
Kahng DH
Lee BE
Park DY
Source :
The Korean journal of gastroenterology = Taehan Sohwagi Hakhoe chi [Korean J Gastroenterol] 2018 Jul 25; Vol. 72 (1), pp. 28-32.
Publication Year :
2018

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.

Details

Language :
Korean
ISSN :
2233-6869
Volume :
72
Issue :
1
Database :
MEDLINE
Journal :
The Korean journal of gastroenterology = Taehan Sohwagi Hakhoe chi
Publication Type :
Academic Journal
Accession number :
30049175
Full Text :
https://doi.org/10.4166/kjg.2018.72.1.28