| Literature DB >> 29602781 |
Katherine A Kaizer-Salk1, Robert J Herten2, Bruce D Ragsdale3, Roberta D Sengelmann1,4.
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. © BMJ Publishing Group Ltd (unless otherwise stated in the text of the article) 2018. All rights reserved. No commercial use is permitted unless otherwise expressly granted.Entities:
Keywords: cancer intervention; dermatology; general practice / family medicine
Mesh:
Year: 2018 PMID: 29602781 PMCID: PMC5878381 DOI: 10.1136/bcr-2017-222751
Source DB: PubMed Journal: BMJ Case Rep ISSN: 1757-790X