Zhang S H, Hu C F, Gao L N, Qiao J F, Li X, Shi S S
Department of Pathology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijinɡ 100021, China.
Zhonghua Bing Li Xue Za Zhi. 2023 Aug 8;52(8):808-813. doi: 10.3760/cma.j.cn112151-20221118-00975.
To investigate the clinicopathological features, immunophenotype and prognosis of nuclear protein in testis (NUT) midline carcinoma. Twenty-four resection cases of NUT midline carcinoma diagnosed at the Department of Pathology, Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China from January 2018 to September 2022, were collected, and retrospectively analyzed for their clinicopathological characteristics. Relevant literature was reviewed. All 24 cases of NUT midline carcinoma occurred in the chest or head and neck, including 14 men and 10 women, with a median age of 40 years. Histological examination showed that the tumors were poorly differentiated, with solid nested or sheet-like arrangement, small to medium-sized cells, sparse cytoplasm and coarse granular chromatin, including 5 cases with abrupt squamous epithelial differentiation. Immunohistochemistry showed that all 24 cases were positive for NUT protein, while 16 cases were p63 positive, 19 cases were p40 positive, 15 out of 18 cases were CK5/6 positive. Follow-up data were obtained for 21 patients (follow-up time range, 1-21 months), of which 11 survived, 10 died, and 3 were lost to follow-up. NUT midline carcinoma is a rare and highly aggressive malignancy with unique histological, immunophenotypic and molecular features. It has a poor prognosis.
探讨睾丸核蛋白(NUT)中线癌的临床病理特征、免疫表型及预后。收集2018年1月至2022年9月在中国北京中国医学科学院肿瘤医院病理科诊断的24例NUT中线癌切除病例,回顾性分析其临床病理特征,并复习相关文献。24例NUT中线癌均发生于胸部或头颈部,其中男性14例,女性10例,中位年龄40岁。组织学检查显示肿瘤分化差,呈实性巢状或片状排列,细胞大小为中到小,胞质稀少,染色质粗糙颗粒状,其中5例有突然的鳞状上皮分化。免疫组化显示24例NUT蛋白均阳性,16例p63阳性,19例p40阳性,18例中的15例CK5/6阳性。获得21例患者的随访数据(随访时间范围1 - 21个月),其中11例存活,10例死亡,3例失访。NUT中线癌是一种罕见且侵袭性强的恶性肿瘤,具有独特的组织学、免疫表型和分子特征,预后较差。