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Plexiform spitz nevus
1Department of Pathology, Nelson R. Mandela School of Medicine, University of Natal, Private Bag 7, Congella 4013, Durban, South Africa.
This study details a rare plexiform Spitz nevus variant in a pediatric patient. It highlights the importance of considering this diagnosis and its differential in similar clinical presentations.
Area of Science:
- Dermatopathology
- Oncology
Background:
- Spitz nevi are melanocytic neoplasms often seen in children and young adults.
- A rare plexiform variant of Spitz nevus was first described in 1999.
Observation:
- A case of plexiform Spitz nevus occurred on the upper thigh of a 10-year-old boy.
- Histological examination revealed epithelioid cell nodules in a plexiform pattern within the dermis.
- Tumor cells showed eosinophilic cytoplasm, vesicular nuclei, prominent nucleoli, and focal intranuclear inclusions.
Findings:
- The tumor was set in a myxoid stroma with lymphocytic and eosinophilic inflammation.
- Melanin-containing spindle cells were occasionally present.
- The differential diagnosis includes various melanocytic and nonmelanocytic lesions with plexiform or myxoid features.
Implications:
- Accurate histological diagnosis is crucial for differentiating plexiform Spitz nevus from other lesions.
- This case adds to the literature on this rare variant, aiding future diagnostic efforts.
- Understanding the histological spectrum of Spitz nevi is important for clinical management.
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