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无色素性黑色素瘤:一项独特的病例研究及文献综述

Amelanotic melanoma: a unique case study and review of the literature.

作者信息

Kaizer-Salk Katherine A, Herten Robert J, Ragsdale Bruce D, Sengelmann Roberta D

机构信息

Santa Barbara Skin Institute, Santa Barbara, California, USA.

Dermatology and Dermatopathology, University of California Irvine School of Medicine, Irvine, California, USA.

出版信息

BMJ Case Rep. 2018 Mar 29;2018:bcr-2017-222751. doi: 10.1136/bcr-2017-222751.

Abstract

Amelanotic melanoma (AM) is a rare form of melanoma which lacks visible pigment. Due to the achromic manifestation of this atypical cutaneous malignancy, it has been difficult to establish clinical criteria for diagnosis. Thus, AM often progresses into an invasive disease due to delayed diagnosis. In this report, we describe the case of a 72-year-old Caucasian woman who had been diagnosed with AM after 3 years of failed treatments for what presented as a periorbital dermatitis. Her Clark's level 4, 1.30 mm thick melanoma required nine surgeries for successful resection and reconstruction. This case exemplifies the diagnostic pitfall of AM and the need for new criteria for early detection and management.

摘要

无色素性黑素瘤(AM)是黑素瘤的一种罕见形式,缺乏可见色素。由于这种非典型皮肤恶性肿瘤的无色表现,很难建立诊断的临床标准。因此,由于诊断延迟,AM常发展为侵袭性疾病。在本报告中,我们描述了一名72岁白种女性的病例,她因眶周皮炎治疗3年失败后被诊断为AM。她的Clark分级为4级,黑素瘤厚度为1.30毫米,成功切除和重建需要进行9次手术。该病例体现了AM的诊断陷阱以及制定早期检测和管理新标准的必要性。

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