Savvidou O D, Sakellariou V I, Papakonstantinou O, Skarpidi E, Papagelopoulos P J
1st Department of Orthopaedics, Athens University Medical School, Attikon University General Hospital, 1 Rimini Street, Chaidari, 12462 Athens, Greece.
Case Rep Orthop. 2015;2015:814241. doi: 10.1155/2015/814241. Epub 2015 Apr 5.
Inflammatory myofibroblastic tumors are uncommon neoplasms; presentation of these tumors in the lower extremities is extremely rare. We present a case of a 47-year-old male with fever, fatigue, and a slow-growing thigh mass. The inflammatory markers were elevated and the MR images showed a well-defined intermuscular lesion with mild heterogeneous enhancement. The lesion was excised and histologic examination was consistent with an inflammatory myofibroblastic tumor. No adjuvant therapy was needed and the patient remained asymptomatic with no evidence of tumor recurrence during the 2 years of follow-up.
炎性肌纤维母细胞瘤是一种罕见的肿瘤;这些肿瘤出现在下肢极为罕见。我们报告一例47岁男性患者,有发热、乏力以及大腿部缓慢生长的肿块。炎症标志物升高,磁共振成像显示一界限清楚的肌间病变,呈轻度不均匀强化。病变被切除,组织学检查符合炎性肌纤维母细胞瘤。无需辅助治疗,患者在2年随访期间无症状,无肿瘤复发迹象。