BAP1‐deficient tumor/nevus with germline aberration: A potential pitfall in assessing melanocytic neoplasms with single nucleotide polymorphism array. (24th May 2019)

• Record Type: Journal Article
• Authors: Hedayat, Amin A.; Lefferts, Joel A.; Atkinson, Aaron E.; Busam, Klaus J.; Linos, Konstantinos
• Is Part Of: Journal of cutaneous pathology. Volume 46:Number 9(2019)
• Page Start: 672
• Page End: 677
• Publication Date: 2019-05-24
• Subjects: BAP‐1 -- germline mutation -- molecular karyotyping -- polymorphism array -- single nucleotide; Skin -- Diseases -- Periodicals; Dermatology -- Periodicals; 616
• DOI: 10.1111/cup.13488
• Languages: English
• ISSNs: 0303-6987

Abstract

Abstract: BRCA1‐associated protein 1 ( BAP1 ) is a tumor suppressor gene, located on chromosome 3p21, encoding BAP1 nuclear protein, which is associated with a subset of melanocytic tumors with distinct cytologic features. Single nucleotide polymorphism array (SNP‐array) is a molecular karyotyping technique that can detect copy number variations and loss of heterozygosity in various fresh and formalin‐fixed paraffin‐embedded tissues. Herein we present a 56‐year‐old female, who presented with a lesion on her left nose/cheek that was growing in size and changing in color. Histopathology was characteristic of a BAP1‐deficient melanocytic neoplasm, with a biphasic population of cytologically bland conventional nevomelanocytes and a proliferation of large epithelioid melanocytes with abundant eosinophilic cytoplasm. Immunohistochemistry for BAP1 showed loss of nuclear labeling in the epithelioid melanocytes. SNP‐array revealed a chromosome 21q22.1 monoaberration with no chromosome 3 abnormalities. The detection of this aberration prompted a discussion as to whether the lesion was best designated as a nevus or tumor. SNP‐array on the patient's blood showed the same monoaberration of chromosome 21q22.1. This case emphasizes the importance of interpreting microarray results in the context of morphology, as germline aberrations can be a pitfall when assessing the genomic stability of a melanocytic proliferation by SNP array.