Volume 39, Issue 12 pp. 1062-1074
Original Article

Expression of p16 alone does not differentiate between Spitz nevi and Spitzoid melanoma

Ashley Mason

Ashley Mason

Department of Dermatology, Yale University School of Medicine, New Haven, CT, USA

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Jade Wititsuwannakul

Jade Wititsuwannakul

Department of Dermatology, Yale University School of Medicine, New Haven, CT, USA

Department of Medicine, Faculty of Medicine, Chulalongkorn University and King Chulalongkorn Memorial Hospital, Thai Red Cross Society, Bangkok, Thailand

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Vincent R. Klump

Vincent R. Klump

Department of Dermatology, Yale University School of Medicine, New Haven, CT, USA

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Jason Lott

Jason Lott

Department of Dermatology, Yale University School of Medicine, New Haven, CT, USA

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Rossitza Lazova

Corresponding Author

Rossitza Lazova

Department of Dermatology, Yale University School of Medicine, New Haven, CT, USA

Rossitza Lazova, MD

15 York Street, P.O. Box 208059, New Haven,

CT 06520-8059, USA

Tel: +1 203 785 4094

Fax: +1 203 785 6869

e-mail: [email protected]

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First published: 29 August 2012
Citations: 58

Abstract

Background

Spitz nevi and Spitzoid melanomas show overlapping histopathologic features, often making the diagnosis challenging. The p16 protein functions as a tumor suppressor and loss of its expression may be seen in some melanomas.

Methods

We evaluated 18 Spitz nevi and 19 Spitzoid melanomas from the Yale Spitzoid Neoplasm Repository for p16 expression. A staining intensity score (SIS) was calculated by multiplying a score for the percentage of stained cells (0–3) by a score for staining intensity (0–3).

Results

Staining with p16 was positive in 15/18 (83%) Spitz nevi and 15/19 (79%) Spitzoid melanomas (p = 0.73). Both Spitz nevi and Spitzoid melanomas had a similar SISs, 4.9 and 3.8, respectively (p = 0.057). All 19 patients with Spitzoid melanomas had poor outcome with either death (6 patients) or metastases (13 patients) at a median (3 years) and mean (5.4 years) follow up. In contrast, all 18 patients with Spitz nevi had a benign course with no adverse events at a median (4 years) and mean (4 years) follow up.

Conclusions

We found no significant difference in p16 staining in Spitz nevi and Spitzoid melanomas. We conclude that p16 does not appear to be a useful immunohistochemical marker in distinguishing between Spitz nevi and Spitzoid melanomas.

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