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Volume 34, Issue 1, Pages 89-92 (January 2003)


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

Minoru Takata, MD, PhD, Keishi Maruo, MD, Toshiro Kageshita, MD, PhD, Shibo Ikeda, MD, Tomomichi Ono, MD, PhD, Fumiaki Shirasaki, MD, PhD, Kazuhiko Takehara, MD, PhD, Boris C. Bastian, MD

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. HUM PATHOL 34:89-92. Copyright 2003, Elsevier Science (USA). All rights reserved.

Department of Dermatology, Kanazawa University Graduate School of Medical Science, Kanazawa, Japan; Department of Dermatology, Kumamoto University School of Medicine, Kumamoto, Japan; and Cancer Center, Department of Pathology, University of California, San Francisco, CA.

 Supported by the Marvin and Roma Auerback Melanoma Fund and a Grant-in Aid for Scientific Research (C2-12670812) from the Japan Society for the Promotion of Science.

☆☆ Address correspondence and reprint requests to Fumiaki Shirasaki, MD, PhD, Department of Dermatology, Kanazawa University Graduate School of Medical Science, 13-1 Takara-machi, Kanazawa 920-8641, Japan.

PII: S0046-8177(03)00004-2

doi:10.1053/hupa.2003.49


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