假性血管肉瘤性鳞状细胞癌:一种罕见的鳞状细胞癌亚型,需与血管肉瘤鉴别,预后较差。

Yuan Zhan, Hongping Wan, Liqing Wu, Xian Ge, Xinhua Xie, Luoyan Wu, Yong Cai
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引用次数: 1

摘要

本研究旨在探讨假血管肉瘤鳞状细胞癌(PASCC)的形成机制。作者回顾了10例PASCC,总结了其临床结局、病理形态特征、免疫表型、治疗方案及相应随访资料。结果病理形态显示复杂的网状结构,其中有大量的吻合束,腔隙结构排列着不典型的肿瘤细胞,与血管肉瘤的组织病理外观相似。特别是,我们观察到复发患者的病理模式与硬化上皮样纤维肉瘤(或黏液样纤维肉瘤)相似。所有病例血管标志物(CD31, ERG)均呈阴性,上皮标志物(CK-pan, p40)呈阳性。参与者的平均年龄为60岁(范围:48-79岁),相对年龄,男女参与者(男性6人,女性4人)无显著差异。肿瘤的位置包括面部(n=3)、上肢(n=1)、腰部(n=1)、宫颈(n=1)、肺部(n=2)、甲状腺(n=1)和乳房(n=1)。所有参与者都接受了4至47个月的临床随访,在此期间,研究人员观察到3名参与者(10名;30%);5名参与者发生远处转移(10人中;50%);2例手术切除部位局部复发;4人死于疾病(10人中;40%),估计中位生存时间为9.5个月,平均生存时间为9个月。结论PASCC有复发和转移的倾向。准确的病理诊断和规范的医疗程序对PASCC的治疗至关重要。PASCC的形成与上皮间充质转化(Epithelial-Mesenchymal Transformation, EMT)和P53基因突变有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pseudoangiosarcomatous squamous cell carcinoma: a rare subtype of squamous cell carcinoma that needs to be differentiated from angiosarcoma and has a poor prognosis.

This study aimed to investigate the formation mechanism of  Pseudoangiosarcoma squamous cell carcinoma (PASCC). The researchers reviewed ten cases of PASCC and summarize their clinical outcomes, pathological morphological traits, immunophenotypes, treatment plans and the corresponding follow-up data. Results showed that the pathological morphology revealed complex reticular structures, where numerous tracts of anastomose, and lacunar structures lined with atypical neoplastic cells, which resembles the histopathological appearance of angiosarcoma. Particularly, we observed pathologic patterns that resemble Sclerosing Epithelioid Fibrosarcoma (or Myxoid Fibrosarcoma) in the patients who suffered a relapse. All cases present negative results for vascular markers (CD31, ERG) and positive results for epithelial markers (CK-pan, p40). The average age of the participants is 60 years old (range: 48-79), relative aged, and there is no significant difference between male and female participants (6 men and 4 women). The locations of neoplasms involve face (n=3), upper limbs (n=1), waist(n=1), cervix uteri (n=1), lungs (n=2), thyroid (n=1), and breasts (n=1). All participants had received clinical follow-ups that range from 4 to 47 months, during which the researchers observed Lymph Node Metastases developed in three participants (out of 10; 30%); Distant Metastases in five participants (out of 10; 50%); two local recurrences at the site of surgical resection; and four deaths due to disease (out of 10; 40%), with 9.5 months estimated median survival time and 9 months mean survival time. It was concluded that PASCC presents the tendency for recurrence and metastasis. Accurate pathological diagnosis and standardized medical procedures are crucial to the treatment of PASCC. Epithelial-Mesenchymal Transformation (EMT) and P53 gene mutation are involved in the formation of PASCC.

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