Duan Jiajia, Wang Ying
Department of Interventional Radiology, China Meitan General Hospital Department of Pathology, Beijing Chaoyang Hospital of Capital Medical University, Beijing, China.
Medicine (Baltimore). 2017 Nov;96(45):e8485. doi: 10.1097/MD.0000000000008485.
Inflammatory myofibroblastic tumor (IMT) is a neoplasm of low malignant potential. The most frequent site of IMT is in the lung, whereas recurrent and metastasis of thyroid IMT has been seldom reported.
A 57-year-old male presented with a 3-year history of painless thyroid mass. The physical examination revealed a diffusely enlarged thyroid which was firm. The thyroid function and antibodies were normal. Thyroid ultrasound revealed a hypoechoic mass in the left lobe and heterogeneous echo in the right lobe. Neck computed tomography showed a diffused enlargement of thyroid with the homogeneously low intensity and the moderate enhancement.
A diagnosis of thyroid IMT was made according the postoperative histological and immunohistochemical analysis.
The patient underwent subtotal thyroidectomy. Seventeen months after the surgery, the patients presented with a firm nodule of right adductor magnus and a relapsing mass of thyroid. Needle core biopsy of the thyroid mass suggested the relapsing of thyroid IMT. The mass excision of the right adductor magnus was performed and an IMT was confirmed by histopathology. The patient underwent thyroid radiation therapy and steroid therapy.
The size of the tumor was smaller than the preradiation size and the patient is now under follow-up.
This is the seldom reported patient with recurrent thyroid IMT with metastasis. IMT of the thyroid is an unusual but distinct disease entity. The clinical and radiological features are not specific and its diagnosis is based on the histological features. Although tumor resection and radiation seem to be effective, no standard treatment for such disease has been established.
炎性肌纤维母细胞瘤(IMT)是一种低恶性潜能的肿瘤。IMT最常见的部位是肺部,而甲状腺IMT的复发和转移鲜有报道。
一名57岁男性,有无痛性甲状腺肿物3年病史。体格检查发现甲状腺弥漫性肿大且质地坚硬。甲状腺功能及抗体正常。甲状腺超声显示左叶有低回声肿物,右叶回声不均匀。颈部计算机断层扫描显示甲状腺弥漫性肿大,密度均匀减低,呈中度强化。
根据术后组织学和免疫组织化学分析,诊断为甲状腺IMT。
患者接受了甲状腺次全切除术。术后17个月,患者出现右大收肌处质地坚硬的结节以及甲状腺肿物复发。甲状腺肿物的粗针穿刺活检提示甲状腺IMT复发。对右大收肌处的肿物进行了切除,组织病理学证实为IMT。患者接受了甲状腺放射治疗和类固醇治疗。
肿瘤大小较放疗前缩小,患者目前正在接受随访。
这是一例鲜有报道的甲状腺IMT复发伴转移患者。甲状腺IMT是一种不常见但独特的疾病实体。其临床和影像学特征不具有特异性,诊断基于组织学特征。虽然肿瘤切除和放疗似乎有效,但尚未确立针对此类疾病的标准治疗方法。