Volume 33, Issue 2 pp. e154-e155
Brief Reports

Spitz Nevus: A Rare Lesion of the Oral Cavity

Mario Vaccaro M.D., Ph.D.

Corresponding Author

Mario Vaccaro M.D., Ph.D.

Division of Dermatology, Department of Clinical and Experimental Medicine, University of Messina, Messina, Italy

Address correspondence to Mario Vaccaro, M.D., Ph.D., Department of Clinical and Experimental Medicine, Dermatology, Via C. Valeria, Gazzi, University of Messina, Messina 98125, Italy, or e-mail: [email protected].Search for more papers by this author
Umberto Romeo D.D.S.

Umberto Romeo D.D.S.

Department of Oral and Maxillo-Facial Sciences, “Sapienza” University of Rome, Rome, Italy

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Carmelo Romeo M.D.

Carmelo Romeo M.D.

Department of Pediatric, Gynecological, Microbiological and Biomedical Sciences, University of Messina, Messina, Italy

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Maria Lentini M.D.

Maria Lentini M.D.

Department of Human Pathology, University of Messina, Messina, Italy

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First published: 21 March 2016
Citations: 2

Abstract

Pigmented mucosal lesions represent a group of rare entities with different etiopathogenetic origins, histopathologic features, dermoscopic appearances, and clinical course. Solitary pigmented lesions of melanocytic origin are uncommon in the oral mucosa, and intraoral occurrence of Spitz nevus is very rare. Here we present a case of Spitz nevus occurring on the hard palate of a 26-month-old boy.

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