| Literature DB >> 28977136 |
Maria Cristina Pedrazini1, Victor Angelo Martins Montalli1, Elemir Macedo de Souza2.
Abstract
OBJECTIVE: To report the clinical evolution and handling of a Spitz nevus, from its initial flat feature to becoming an irregular, nodular, reddish lesion. CASE DESCRIPTION: Female child, phototype II, with a small congenital nevus on the left lower limb and other sustained small nevi. The patient went through annual clinical and dermoscopic evaluations between the ages of three and seven, period during which the nevi located on the left thigh grew rapidly. The clinical hypothesis was Spitz nevus, with indication of surgical removal with a safety margin and anatomopathological study. Considering patient's age and clinical/histological aspects, the diagnosis of Spitz nevus was confirmed. COMMENTS: Initial globular pattern and size under 5 mm upon dermoscopy allowed clinical follow-up. However, onset of hyperchromia and rapid growing of the lesion, along with aesthetic concerns, possibility of trauma in the region, and risk of malignancy at puberty guided the decision of total resection and follow-up for recurrence.Entities:
Mesh:
Year: 2017 PMID: 28977136 PMCID: PMC5737265 DOI: 10.1590/1984-0462/;2017;35;4;00016
Source DB: PubMed Journal: Rev Paul Pediatr ISSN: 0103-0582
Figure 1:Digital dermoscopy: (A) 1 mm in February 2010; (B) 1.5 mm in March 2011.
Figure 2:Nevus clinical evolution: (A) 2.0 mm in February 2012; (B-E) 4.5 mm in March 2013.
Growth follow-up: left thigh nevus.
Figure 3:Photomicrograph of Spitz nevus histological sections stained with hematoxylin and eosin (HE) for light optical microscopy: (A) epithelial expansion showing free borders (40x magnification); (B) melanocytic nests (200x magnification); (C) characteristic HE-stained Kamino bodies underlying the epithelium (400x magnification).