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原发性肺透明细胞肉瘤——首例报告的两例病例

Primary pulmonary clear cell sarcoma-the first two reported cases.

作者信息

Goh Giap Hean, Teh Ming, Vanecek Tomas, Moran Cesar, Petersson Fredrik

机构信息

Department of Pathology, National University Health System, 5 Lower Kent Ridge Road, 119074, Singapore.

Department of Molecular Genetics, Bioptical Laboratory Ltd, Pilsen, Czech Republic.

出版信息

Virchows Arch. 2016 Jul;469(1):111-7. doi: 10.1007/s00428-016-1943-8. Epub 2016 Apr 25.

Abstract

We report two cases (male patients 50 and 55 years old) of clear cell sarcoma ("melanoma of soft parts") arising in the lung, of which one case showed regional lymph node metastases. Histologically, both tumors displayed varying clear epithelioid and spindle neoplastic cells arranged in storiform and nested growth patterns, separated by thin fibrovascular septa. Immunohistochemical studies demonstrated positive expression of S-100 protein, HMB-45 and Melan-A in one case and S-100 protein only in the other. Fluorescence in situ hybridization showed positive EWSR1 gene rearrangement, and a presence of EWS-ATF1 fusion transcript was confirmed by RT-PCR and sequencing in one case.

摘要

我们报告了两例发生于肺部的透明细胞肉瘤(“软组织黑色素瘤”)病例(男性患者,年龄分别为50岁和55岁),其中一例出现区域淋巴结转移。组织学上,两个肿瘤均显示出不同程度的透明上皮样和梭形肿瘤细胞,呈束状和巢状生长模式,被薄的纤维血管间隔分隔。免疫组化研究显示,一例中S-100蛋白、HMB-45和Melan-A呈阳性表达,另一例仅S-100蛋白呈阳性。荧光原位杂交显示EWSR1基因重排阳性,其中一例经逆转录聚合酶链反应(RT-PCR)和测序证实存在EWS-ATF1融合转录本。

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