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一名13岁男孩的软组织浅表黏膜下透明细胞肉瘤,类似黑色素瘤。

Superficial paramucosal clear cell sarcoma of the soft parts resembling melanoma in a 13-year-old boy.

作者信息

Sidiropoulos Michael, Busam Klaus, Guitart Joan, Laskin William B, Wagner Annette M, Gerami Pedram

机构信息

Department of Dermatology, Feinberg School of Medicine, Northwestern University, Chicago, IL 60611, USA.

出版信息

J Cutan Pathol. 2013 Feb;40(2):265-8. doi: 10.1111/cup.12058. Epub 2012 Dec 10.

Abstract

Clear cell sarcoma (CCS) of tendons and aponeuroses, also known as melanoma of soft parts, represents an aggressive rare malignancy that is characterized by a nested or fascicular pattern of spindled cells and a pathognomonic reciprocal translocation, t(12;22)(q13;q12), that results in the fusion of EWSR1 and ATF1 genes. Numerous recent studies have recognized the importance of a cutaneous CCS variant that can mimic a broad spectrum of entities, including spindle cell melanoma, spindle cell squamous carcinoma, cutaneous leiomyosarcoma and atypical fibroxanthoma. We report a case of a 13-year-old boy with cutaneous CCS who presented with a few months history of an asymptomatic papule on the lower lip that was suggestive of a mucocele. Biopsy of the lesion showed a wedge shaped neoplasm arranged in nests and fascicles of epithelioid- to oval-shaped cells with pale cytoplasm, open chromatin and prominent nucleolus. The superficial component was closely opposed to the basal epithelium resembling the junctional nests of a melanocytic neoplasm. The process extended into and involved the striated muscle of the lip. The cells expressed S-100, CD99 and synaptophysin by immunohistochemistry, and there was focal HMB-45 and microphthalmia transcription factor (MiTF) positivity as well. Fluorescence in situ hybridization confirmed the presence of the t(12;22) (ESWR1-ATF1) translocation.

摘要

肌腱和腱膜透明细胞肉瘤(CCS),也称为软组织黑色素瘤,是一种侵袭性罕见恶性肿瘤,其特征为梭形细胞呈巢状或束状排列,以及特征性的相互易位t(12;22)(q13;q12),该易位导致EWSR1和ATF1基因融合。最近的大量研究已经认识到皮肤CCS变异型的重要性,它可以模仿多种病变,包括梭形细胞黑色素瘤、梭形细胞鳞状癌、皮肤平滑肌肉瘤和非典型纤维黄色瘤。我们报告一例13岁患有皮肤CCS的男孩,其下唇出现一个无症状丘疹,病史为几个月,提示黏液囊肿。病变活检显示为楔形肿瘤,由上皮样至椭圆形细胞的巢状和束状结构组成,细胞质淡染,染色质开放,核仁突出。浅表部分紧邻基底上皮,类似于黑素细胞肿瘤的交界性巢。病变延伸至并累及唇部的横纹肌。免疫组化显示细胞表达S-100、CD99和突触素,也有局灶性HMB-45和小眼转录因子(MiTF)阳性。荧光原位杂交证实存在t(12;22)(ESWR1-ATF1)易位。

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