Recurrent retroperitoneal inflammatory myofibroblastic tumor: A case report

Oncol Lett. 2016 Aug;12(2):1535-1538. doi: 10.3892/ol.2016.4767. Epub 2016 Jun 23.

Abstract

Inflammatory myofibroblastic tumor (IMT), which was previously known as inflammatory pseudotumor, is characterized by myofibroblastic spindle cells accompanied by inflammatory infiltrates. IMT is a rare lesion of unclear etiology, which induces non-specific clinical symptoms. The present case report describes a 74-year-old female patient with recurrent IMT, which was successfully re-resected 30 months subsequent to initial surgical removal. The patient presented with left hydroureteronephrosis and a 10-cm paravertebral mass which, upon surgery, was found to involve the descending colon. Successful, complete en bloc re-resection was achieved, and at 24 months follow-up, the patient remained clinically free of disease. Complete surgical extirpation, where feasible, is the recommended treatment for primary and recurrent IMT lesions.

Keywords: recurrent; retroperitoneal inflammatory myofibroblastic tumor; surgery.