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皮肤淋巴结瘤

Cutaneous lymphadenoma.

作者信息

Alsadhan Aziz, Taher Moba, Shokravi Mohammad

机构信息

Division of Dermatology, University of Alberta, Edmonton, Alberta, Canada.

出版信息

J Am Acad Dermatol. 2003 Dec;49(6):1115-6. doi: 10.1016/s0190-9622(03)00455-9.

Abstract

Cutaneous lymphadenoma is a rare tumor with distinctive histologic features. This entity was originally described as lymphoepithelial tumor by Santa Cruz and Barr in 1987. It was renamed cutaneous lymphadenoma in 1991. To date, at least 31 cases of this entity have been reported. The literature did not contain a clinical photograph of this lesion. A case of this rare tumor is described that includes clinical and histologic features. The literature regarding the unclear histogenesis of this distinctive tumor is reviewed. This report is one of a only few clinical illustrations of cutaneous lymphadenoma. Consistent with previous reports, the histologic findings in this case include basaloid proliferation and intraepithelial lymphocytes. The usual initial clinical diagnosis is basal cell carcinoma localized mainly to the head and neck area. The incidence is approximately equal in male and female patients. Excision of this benign neoplasm is curative. Controversy exists regarding the histogenesis of this tumor.

摘要

皮肤淋巴结瘤是一种具有独特组织学特征的罕见肿瘤。该实体最初由圣克鲁斯和巴尔于1987年描述为淋巴上皮瘤。1991年被重新命名为皮肤淋巴结瘤。迄今为止,至少已报道了31例该实体病例。文献中没有该病变的临床照片。本文描述了一例这种罕见肿瘤的病例,包括临床和组织学特征。对关于这种独特肿瘤组织发生不明的文献进行了综述。本报告是皮肤淋巴结瘤仅有的少数临床例证之一。与先前的报告一致,该病例的组织学发现包括基底样增生和上皮内淋巴细胞。通常最初的临床诊断是主要局限于头颈部区域的基底细胞癌。男性和女性患者的发病率大致相等。切除这种良性肿瘤可治愈。关于该肿瘤的组织发生存在争议。

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