| Literature DB >> 25309095 |
Jun-Jie Zhao1, Jia-Qian Ling1, Yong Fang1, Xiao-Dong Gao1, Ping Shu1, Kun-Tang Shen1, Jing Qin1, Yi-Hong Sun1, Xin-Yu Qin1.
Abstract
Inflammatory myofibroblastic tumors are usually treated by surgical resection. We herein report two cases of intra-abdominal inflammatory myofibroblastic tumors that were unresectable and underwent spontaneous regression without any treatment. Our case report and literature review show that regression is more common in the middle-aged and older male populations. Abdominal discomfort and fever were the most common symptoms, but the majority of patients had no obvious physical signs. There was no specific indicator for diagnosis. The majority of the lesions regressed within 3 mo and nearly all of the masses completely resolved within 1 year. We conclude that the clinical characteristics of inflammatory myofibroblastic tumors are variable and, accordingly, the disease needs to be subdivided and treated on an individual basis. Surgery is always the first-line treatment; however, for those masses assessed as unresectable, conservative therapy with intense follow-up should be considered.Entities:
Keywords: Abdominal cavity; Inflammatory myofibroblastic tumor; Inflammatory pseudotumor; Spontaneous regression
Mesh:
Year: 2014 PMID: 25309095 PMCID: PMC4188916 DOI: 10.3748/wjg.v20.i37.13625
Source DB: PubMed Journal: World J Gastroenterol ISSN: 1007-9327 Impact factor: 5.742