表现为巨大胃假性肿瘤的炎性肌纤维组织细胞增生

Inflammatory myofibrohistiocytic proliferation presenting as giant gastric pseudotumor.

作者信息

Marn C S, Hsu F K

机构信息

Department of Radiology, University of Michigan Medical Center, Ann Arbor.

出版信息

Gastrointest Radiol. 1992 Fall;17(4):316-8. doi: 10.1007/BF01888577.

DOI:10.1007/BF01888577

PMID:1426846

Abstract

A 5-year-old boy presented with refractory microcytic anemia, growth failure, and markedly elevated sedimentation rate. Computed tomographic (CT) and upper gastrointestinal study disclosed an ulcerated 9-cm large gastric mass, which proved to be an inflammatory myofibrohistiocytic proliferation (IMP). The characteristic clinical and radiologic features of this rare entity are herein reviewed.

摘要

一名5岁男孩出现难治性小细胞贫血、生长发育迟缓以及血沉显著升高。计算机断层扫描（CT）和上消化道检查发现一个9厘米大的溃疡型胃肿物，经证实为炎性肌纤维组织细胞增生（IMP）。本文回顾了这一罕见病症的特征性临床和影像学表现。