Viswanathan Seethalakshmi, Rahman Khaliqur, Pallavi Suryawanshi, Sachin Johari, Patil Asawari, Chaturvedi Pankaj, D'Cruz Anil, Agarwal Jaiprakash, Kane S V
Department of Pathology, Tata Memorial Hospital, 8th Floor, Annexe Building, Ernst Borges Road, Parel, Mumbai 400012, India.
Head Neck Pathol. 2010 Dec;4(4):265-75. doi: 10.1007/s12105-010-0204-4. Epub 2010 Aug 22.
Sarcomatoid carcinomas are biphasic tumors proven to be monoclonal dedifferentiated forms of conventional squamous carcinomas. This study evaluates their clinicopathologic characteristics in head and neck mucosal sites and the problems in distinguishing them from other spindle cell tumors. A total of 103 cases with a confirmed diagnosis of sarcomatoid carcinoma accessioned in the pathology department of a tertiary referral cancer centre over a period of 7 years (2004-2010) were studied. An algorithm used for their diagnosis is presented. Ages of the patients were 22-90 years (median 53 years), and male:female ratio was 3.7:1. Site distribution was oral cavity (n = 65, 63.1%), larynx (18, 17.5%), oropharynx/hypopharynx (12, 10.7%), maxilla (6, 5.8%) and metastatic nodes (2, 1.9%). A large number of patients (95%) presented with a mass lesion of less than 1 year duration. Histopathologically, epithelial differentiation was evident on morphology in 48 (46.6%) cases, only on IHC in 34 (33%) cases, and in 21 (20.4%) no epithelial differentiation was seen. Typically, tumors were polypoidal (92, 89.3%) and ulcerated (95, 92.2%) with cells arranged predominantly in fascicles (59, 57.3%) or storiform pattern (17, 16.5%) amidst collagenous (50, 48.5%) or myxoid matrix (35, 34%). Anaplasia (2+/3+) and mitosis >10 per 10 HPF were noted in 96 (93.2%) cases. IHC was done in 82 cases; 55 (66.7%) showed positivity for epithelial markers with aberrant expression of mesenchymal markers in 43 (41.7%). Diagnosis of sarcomatoid squamous carcinoma is challenging because of overlapping histopathological features with other spindle cell tumors. Understanding their clinicopathologic characteristics facilitates their diagnosis and appropriate clinical management.
肉瘤样癌是一种双相性肿瘤,已被证实是传统鳞状细胞癌的单克隆去分化形式。本研究评估了它们在头颈部黏膜部位的临床病理特征以及将其与其他梭形细胞肿瘤区分开来时存在的问题。对一家三级转诊癌症中心病理科在7年期间(2004 - 2010年)确诊的103例肉瘤样癌病例进行了研究。本文介绍了一种用于其诊断的算法。患者年龄为22 - 90岁(中位年龄53岁),男女比例为3.7:1。部位分布为口腔(n = 65,63.1%)、喉(18,17.5%)、口咽/下咽(12,10.7%)、上颌骨(6,5.8%)和转移淋巴结(2,1.9%)。大量患者(95%)表现为病程少于1年的肿块病变。组织病理学上,48例(46.6%)在形态学上有明显的上皮分化,34例(33%)仅在免疫组化上有上皮分化,21例(20.4%)未见上皮分化。典型的肿瘤呈息肉状(92例,89.3%)且有溃疡(95例,92.2%),细胞主要排列成束状(59例,57.3%)或席纹状(17例,16.5%),位于胶原性(50例,48.5%)或黏液样基质中(35例,34%)。96例(93.2%)可见间变(2+/3+)且每10个高倍视野有>10个核分裂象。对82例进行了免疫组化检查;55例(66.7%)上皮标志物呈阳性,43例(41.7%)间充质标志物有异常表达。由于与其他梭形细胞肿瘤的组织病理学特征重叠,肉瘤样鳞状癌的诊断具有挑战性。了解它们的临床病理特征有助于其诊断及适当的临床处理。