Two cases of unusual acral melanocytic tumors: illustration of molecular cytogenetics as a diagnostic tool

Hum Pathol. 2003 Jan;34(1):89-92. doi: 10.1053/hupa.2003.49.

Abstract

The differential diagnosis between benign Spitz nevus and malignant melanoma may present considerable difficulties in some cases. Here we report 2 unusual melanocytic tumors with spitzoid features developing in acral sites of Japanese patients to illustrate the use of comparative genomic hybridization (CGH) to classify these lesions. Case 1 was a 12-mm-thick, >2 cm-diameter nodule on the sole of a 37-year-old man. Case 2 was a subungual tumor of the left index finger in a 13-year-old boy. CGH showed absence of chromosomal aberrations in case 1 and multiple aberrations in case 2, including focused amplification as previously described in acral melanomas. Case 1 was free of disease after 2.5 years of follow-up, whereas case 2 developed lymph node metastasis. We conclude that molecular techniques such as CGH can be of diagnostic help in the classification of histologically ambiguous lesions.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Chromosomes, Human, Pair 11
  • Chromosomes, Human, Pair 5
  • DNA, Neoplasm / analysis
  • Diagnosis, Differential
  • Extremities / pathology
  • Humans
  • Immunohistochemistry
  • Male
  • Melanocytes / pathology*
  • Melanoma / diagnosis*
  • Melanoma / genetics
  • Melanoma / secondary
  • Nevus, Epithelioid and Spindle Cell / diagnosis*
  • Nevus, Epithelioid and Spindle Cell / genetics
  • Nucleic Acid Hybridization*
  • Skin Neoplasms / diagnosis*
  • Skin Neoplasms / genetics

Substances

  • DNA, Neoplasm