Metastatic Acral lentiginous melanoma: A case report and review

Of the four subtypes of cutaneous melanoma, acral lentiginous melanoma (ALM) is atypical in its presentation. ALM is a rare melanoma subtype that presents on the volar surfaces of the hand and foot. The difficulty of making an early diagnosis of ALM is highlighted by the case seen in our institution...

Full description

Saved in:
Bibliographic Details
Published in:Journal of the National Medical Association Vol. 114; no. 3; pp. 290 - 294
Main Authors: Ahuja, Geeta, Kim, Jae Ho, Tran, Joseph Francis, Nnorom, Siobhan, Ali, Ahmed, Ibrahim, Mohammed, Okoye, Ginette A, Shokrani, Babak, Dunmore-Griffith, Jacqueline, Geter, Kirk, Frederick, Wayne A I, Wilson, Lori
Format: Report
Language:English
Published: 01-06-2022
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:Of the four subtypes of cutaneous melanoma, acral lentiginous melanoma (ALM) is atypical in its presentation. ALM is a rare melanoma subtype that presents on the volar surfaces of the hand and foot. The difficulty of making an early diagnosis of ALM is highlighted by the case seen in our institution. The dire prognosis associated with ALM is postulated to be not only related to its destructive nature, but also due to a lack of patient awareness and vigilance, inadequate physician awareness, and disparity in healthcare access. We present this as a unique account of an ALM lesion in a 76 year old African-American male presenting originally in the left foot that went misdiagnosed for several years. The original lesion was considered to be an ulcerating left great toe lesion with signs typical of osteomyelitis. These clinical findings were corroborated by radiological x-ray evidence. Upon amputation and biopsy for suspected worsening osteomyelitis five years later, the pathological diagnosis of melanoma was finally made.
Bibliography:ObjectType-Case Study-2
content type line 59
SourceType-Reports-1
ObjectType-Report-1
ISSN:1943-4693
DOI:10.1016/j.jnma.2022.01.011