Jundishapur Journal of Oncology;2015, December; Current Issue Article Farsi Title: Inflammatory Myofibroblastic Tumor of Pelvic Cavity in a 17- Year- Old Girl with Previous History of Wilms’ Tumor: A Case Report
Article Farsi Keywords: Background: Existence of Synchronous or metachronous tumors in one patient is a rare phenomenon. However, some genetically controlled processes can lead to multiple tumors in one patient. Inflammatory myofibroblastic tumor is a rare neoplasm that usually happens in the lung and the usual location for extra pulmonary presentation is kidney. Case Report: In following article we report a 17- year old girl presented with hypo gastric abdominal pain fever and malaise which CT scan showed a huge mass in the pelvic cavity. The patient previously underwent left nephrectomy
due to Wilms’ tumor in childhood. The pathology report of the resected pelvic mass showed the spindle cell tumor and
inflammatory myofibroblastic neoplasm.
Conclusion: Despite improvement in diagnostic procedures, the precise diagnosis of myofibroblastic tumor remains
highly dependent on surgery and following pathologic assessments.
نویسندگان این مقاله
1-Inflammatory Myofibroblastic Tumor of Pelvic Cavity in a 17- Year- Old
Girl with Previous History of Wilms’ Tumor: A Case Report