| Literature DB >> 26765239 |
Rafael Cholvi-Calduch1, María Carmen Fernández-Moreno2, María Díaz-Tobarra3, Julio Calvete-Chornet4.
Abstract
INTRODUCTION: Inflammatory myofibroblastic tumors (IMT) are rare neoplasms characterized by a proliferation of spindle-shaped cells with a stroma infiltrated by macrophages, lymphocytes and plasma cells. CASE REPORT: We report a case of 59 years old male who presented an acute abdomen due to a mass of the mesentery of the terminal ileum, which was perforated with active bleeding. Histopathology reported a low-grade TMI with clear margins. DISCUSSION: Inflammatory myofibroblastic tumors of the mesentery are rare entities whose etio-pathogenia remains unclear. It requires a histopathological diagnosis and inmunohistochemical evaluation and its treatment is based on complete resection of the tumor. These type of neoplasms require close monitoring due to local recurrence.Entities:
Mesh:
Year: 2016 PMID: 26765239
Source DB: PubMed Journal: Rev Esp Enferm Dig ISSN: 1130-0108 Impact factor: 2.086