Shah Aadit, Pey Eduard, Achonu Justice U, Bai Ji Dong K, Khan Fazel
Department of Orthopaedics, Stony Brook University Hospital, Stony Brook, NY, USA.
Stony Brook University Renaissance School of Medicine, Stony Brook, NY, USA.
Orthop Res Rev. 2021 Oct 2;13:163-169. doi: 10.2147/ORR.S333124. eCollection 2021.
Inflammatory myofibroblastic tumors (IMTs) are mesenchymal neoplasms most seen in the abdominopelvic region, lung, and retroperitoneum; and less commonly seen in virtually any other site. We report a case of two lower limb masses consistent with diagnosis of IMTs. This is a 39-year-old woman with a history of right lower extremity popliteal fossa synovial sarcoma diagnosed 12 years prior and treated with chemotherapy, surgery, and radiation. She presented with two new - one anterior and one posterior - right thigh masses. Biopsies of the lesions demonstrated low-grade inflammatory spindle cell lesions at both sites. Wide resection was performed for both masses and further characterization of the surgical specimens was most consistent with IMT. At follow-up, the patient is well with no signs of recurrence 19 and 7 months postoperative to the resection of the anterior and posterior thigh masses, respectively. This case represents the first reported IMTs occurring as late as 12 years after primary cancer treatment, and the first occurring after synovial sarcoma.
炎性肌纤维母细胞瘤(IMTs)是一种间叶性肿瘤,多见于腹盆腔区域、肺部和腹膜后;在几乎任何其他部位都较少见。我们报告一例双下肢肿块病例,诊断为IMTs。这是一名39岁女性,12年前曾诊断为右下肢腘窝滑膜肉瘤,接受过化疗、手术和放疗。她出现了两个新的肿块,一个在右大腿前部,一个在右大腿后部。病变活检显示两个部位均为低级别炎性梭形细胞病变。对两个肿块均进行了广泛切除,手术标本的进一步特征与IMT最为相符。随访时,分别在切除大腿前部和后部肿块术后19个月和7个月,患者情况良好,无复发迹象。该病例是首次报道的IMTs发生在原发性癌症治疗后长达12年,也是首次发生在滑膜肉瘤之后。