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Polypoid Spitz Nevus With a Halo Reaction.
Angel Fernandez-Flores1, Marcela Saeb-Lima, José Luis Rodriguez-Peralto
1*Department of Cellular Pathology, Hospital El Bierzo, Ponferrada, Spain;†Department of Pathology, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, INER/CIENI, Hospital Angeles Lomas, Centro Medico ABC, Mexico City, Mexico; and‡Department of Pathology, Hospital Universitario 12 de Octubre, Universidad Complutense, I+12, Madrid, Spain.
This report details a rare case of polypoid Spitz nevus with a halo reaction in a 10-year-old boy. This uncommon presentation showed no significant genetic aberrations and has not recurred after two years.
Area of Science:
- Dermatopathology
- Oncology
- Genetics
Background:
- Spitz nevi are melanocytic tumors with varying presentations.
- Polypoid morphology and halo reactions are individually uncommon in Spitz nevi.
- The co-occurrence of polypoid morphology and halo reaction is exceptionally rare.
Observation:
- A 10-year-old male presented with a polypoid Spitz nevus exhibiting a halo reaction on his back.
- The lesion was evaluated for specific molecular markers and genetic alterations.
- Clinical follow-up was conducted to monitor for recurrence.
Findings:
- The Spitz nevus demonstrated preserved nuclear expression of BAP1.
- Immunohistochemistry revealed no expression of BRAF and ALK, but p16 expression was noted in melanocytic cells.
- Comparative genomic hybridization identified only minor losses on chromosome 8, with no significant aberrations.
Implications:
- This case expands the known spectrum of Spitz nevus presentations.
- The findings contribute to understanding the molecular profile of rare Spitz nevus variants.
- The absence of significant genetic aberrations and recurrence suggests a benign clinical course for this specific presentation.
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