Wang Li, Liu WangWang, Tang Wen, Ma Yan, Liu Xi Bo, Liu Fang
Department of Pathology, Shaoxing People's Hospital, School of Medicine, Shaoxing University, Shaoxing, 312000, Zhejiang, China.
Department of Pathology, Sir Run Run Shaw Hospital, Hangzhou, 310009, Zhejiang, China.
Discov Oncol. 2025 Feb 12;16(1):170. doi: 10.1007/s12672-025-01941-5.
Capicua transcriptional repressor (CIC)-rearranged sarcoma (CRS) is a rare and highly aggressive malignant soft tissue small round cell sarcoma. Most CRS tumors occur in the soft tissues of the limbs and trunk and cases in the thyroid gland are extremely rare, with no extant reports in an adult thyroid. This report aims to familiarize clinicians and pathologists with CRS in the thyroid gland, thereby helping them identify new cases, and provide pathological evidence for comprehensive diagnosis and treatment. A 30-year-old woman presented with an asymptomatic right thyroid mass of 5 months. Neck ultrasonography revealed a hypoechoic hypervascular nodule with a maximum diameter of 5 cm. The noncalcified nodule was classified as Ti-RADS 4a. Besides thyroid dysfunction, her thyroglobulin and anti-thyroid peroxidase antibody concentrations were 35.83 IU/mL and > 1,000.00 IU/mL, respectively. CRS was diagnosed based on the histomorphology, immunohistochemistry, and molecular genetics results. The patient opted for further treatment at Zhejiang Cancer Hospital. Ten months after surgical removal, positron emission tomography/computed tomography revealed tumor metastasis to the cervical lymph nodes and lungs. In February 2023, the patient underwent postoperative adjuvant radiotherapy for the tumor bed and cervical lymph nodes and received doses of PGTVtb 6,000 cGy/30F/DT and PTV 5,400 cGy/30F/DT. The patient last visited the clinic in May 2024 due to fever, fatigue, diarrhea, and other symptoms. CRS in solid organs is extremely rare; however, when the morphology shows multinodular, small, round cells with mild-to-moderate atypia, vacuolated nuclei, and prominent nucleoli, it should be considered as a potential differential diagnosis.
Capicua转录抑制因子(CIC)重排肉瘤(CRS)是一种罕见且侵袭性极强的恶性软组织小圆细胞肉瘤。大多数CRS肿瘤发生于四肢和躯干的软组织,发生于甲状腺的病例极为罕见,目前尚无成人甲状腺CRS的报道。本报告旨在使临床医生和病理学家熟悉甲状腺CRS,从而帮助他们识别新病例,并为综合诊断和治疗提供病理依据。一名30岁女性出现无症状的右侧甲状腺肿物5个月。颈部超声检查显示一个最大直径为5cm的低回声高血运结节。该非钙化结节被分类为甲状腺影像报告和数据系统(TI-RADS)4a类。除甲状腺功能异常外,她的甲状腺球蛋白和抗甲状腺过氧化物酶抗体浓度分别为35.83IU/mL和>1000.00IU/mL。根据组织形态学、免疫组化和分子遗传学结果诊断为CRS。患者选择在浙江省肿瘤医院进一步治疗。手术切除10个月后,正电子发射断层扫描/计算机断层扫描显示肿瘤转移至颈部淋巴结和肺部。2023年2月,患者接受了针对瘤床和颈部淋巴结的术后辅助放疗,靶区(PGTVtb)剂量为6000cGy/30次分割/总剂量,计划靶区(PTV)剂量为5400cGy/30次分割/总剂量。患者因发热、乏力、腹泻等症状于2024年5月最后一次就诊。CRS在实体器官中极为罕见;然而当形态学表现为多结节、小圆形细胞,伴有轻至中度异型性、核空泡化和核仁明显时,应考虑作为潜在的鉴别诊断。