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近端型上皮样肉瘤:20例临床病理研究

Proximal-type epithelioid sarcoma: a clinicopathologic study of 20 cases.

作者信息

Hasegawa T, Matsuno Y, Shimoda T, Umeda T, Yokoyama R, Hirohashi S

机构信息

Pathology Division, National Cancer Center Research Institute and Hospital, Tokyo, Japan.

出版信息

Mod Pathol. 2001 Jul;14(7):655-63. doi: 10.1038/modpathol.3880368.

Abstract

We studied the clinicopathologic and immunohistochemical features of 20 cases of proximal-type epithelioid sarcoma to identify prognostic factors. The 20 patients ranged in age from 13 to 80 years (mean, 40 y); 12 patients were male and 8 were female. The tumors presented as deep soft-tissue or subcutaneous masses on the inguinal region in five, the thigh in four, the vulva in three, the axilla in three, and one each in the flank, chest wall, back, hip and perineum. The tumors ranged from 2 to 16 cm at their greatest diameter (mean: 7.8 cm). Histologically, 12 tumors (60%) were classified as the large-cell subtype, characterized by sheets of large cells with prominent nucleoli resembling poorly differentiated carcinoma, and a frequent rhabdoid phenotype, six (30%) were classified as the conventional subtype, and two (10%) as the angiomatoid subtype. The numbers of tumors exhibiting immunoreactivity for various markers were: vimentin (20 cytokeratin (20 [100%]); epithelial membrane antigen (17 [85%]); CD34 (9 [45%]); CD99 (5 [25%]); muscle markers, either desmin or alpha-smooth muscle actin (3 [15%]), other markers such as S-100 protein, neurofilament, neuron-specific enolase, synaptophysin and CD56 (12 [60%]); and p53 (16 [80%]). Fourteen lesions (70%) exhibited an MIB-1 index of 30% or more and, by a system of histologic grading using the MIB-1 score, 16 tumors (80%) were classified as high-grade (Grade 3). Thirteen patients (65%) developed local recurrence and 15 (75%) had metastases, primarily to the lymph nodes. At the last follow-up, 13 patients (65%) had died of their disease. A large tumor size and early metastasis were independently associated with a poor outcome. We conclude that proximal-type epithelioid sarcomas are rare, undifferentiated soft-tissue sarcomas of adults, with epithelioid features and a frequent rhabdoid phenotype. These tumors, when arising in proximal locations, have a much worse prognosis than those arising in distal locations.

摘要

我们研究了20例近端型上皮样肉瘤的临床病理及免疫组化特征,以确定预后因素。20例患者年龄范围为13至80岁(平均40岁);男性12例,女性8例。肿瘤表现为腹股沟区深部软组织或皮下肿块5例,大腿4例,外阴3例,腋窝3例,侧腹、胸壁、背部、臀部和会阴各1例。肿瘤最大直径为2至16厘米(平均7.8厘米)。组织学上,12例肿瘤(60%)被分类为大细胞亚型,其特征为成片的大细胞,核仁明显,类似低分化癌,且常见横纹肌样表型;6例(30%)被分类为传统亚型,2例(10%)为血管瘤样亚型。对各种标志物呈免疫反应的肿瘤数量分别为:波形蛋白(20例)、细胞角蛋白(20例[100%])、上皮膜抗原(17例[85%])、CD34(9例[45%])、CD99(5例[25%])、肌肉标志物(结蛋白或α平滑肌肌动蛋白,3例[15%])、其他标志物(如S-100蛋白、神经丝、神经元特异性烯醇化酶、突触素和CD56,12例[60%])以及p53(16例[80%])。14个病灶(70%)的MIB-1指数为30%或更高,通过使用MIB-1评分的组织学分级系统,16例肿瘤(80%)被分类为高级别(3级)。13例患者(65%)发生局部复发,15例(75%)发生转移,主要转移至淋巴结。在最后一次随访时,13例患者(65%)死于该病。肿瘤体积大及早期转移与预后不良独立相关。我们得出结论,近端型上皮样肉瘤是成人罕见的未分化软组织肉瘤,具有上皮样特征且常见横纹肌样表型。这些肿瘤发生于近端部位时,预后比发生于远端部位的肿瘤差得多。

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