| Literature DB >> 35535202 |
Andrew S Kao1, Kayla St Claire2, Lisa M Bedford2, Darius R Mehregan2, Aleodor A Andea3, David Kouba2,4.
Abstract
Nevoid and myxoid melanoma are rare variants of melanoma; association of the two is a unique finding. Nevoid melanoma is characterized by morphologic resemblance to a nevus, whereas myxoid melanoma demonstrates a basophilic mucinous matrix. We present an atypical case of a melanoma progressing from a nevoid melanocytoma with myxoid changes. A 78-year-old female presented with a pigmented growth on her right thigh. Biopsy demonstrated a biphenotypic melanocytic proliferation composed of a nodule showing epithelioid melanocytes with enlarged nuclei, prominent nucleoli, lack of maturation, and abundant amphophilic cytoplasm with a rare mitotic figure. These findings were suggestive of melanoma along with a nevoid dermal component and myxoid stroma. FISH testing revealed a homozygous loss of 9p21 in the atypical component. SNP-microarray from the nevoid component demonstrated three abnormalities including a gain of whole chromosome 8, as well as loss of a copy of nearly an entire chromosome 9 and 16q most consistent with a melanocytoma. IJCEPEntities:
Keywords: Myxoid melanoma; malignant melanoma; melanocytoma; nevoid melanoma
Year: 2022 PMID: 35535202 PMCID: PMC9077108
Source DB: PubMed Journal: Int J Clin Exp Pathol ISSN: 1936-2625