Pediatric CD8+/CD56+ mycosis fungoides with cytotoxic marker expression: A variant with indolent course

Marco Rovaris1, Chiara Colato2, Giampiero Girolomoni1

  • 1Department of Medicine, Section of Dermatology and Venereology, University of Verona, Verona, Italy.

Insights

This study details a rare pediatric case of CD8+/CD56+ mycosis fungoides in a 10-year-old boy. The condition showed a favorable prognosis with skin-directed treatments, achieving complete remission.

Area of Science:

  • Pediatric Dermatology
  • Oncoimmunology

Background:

  • Mycosis fungoides (MF) is a rare cutaneous T-cell lymphoma, typically affecting adults.
  • Pediatric MF, while uncommon, presents unique diagnostic and therapeutic challenges.

Observation:

  • A 10-year-old boy presented with asymptomatic, erythematous, and scaling plaques on the thigh and trunk.
  • Biopsy revealed CD8+/CD56+ mycosis fungoides with expression of cytotoxic markers (perforin, TIA-1, granzyme B).

Findings:

  • The patient achieved complete remission within 2 months using narrow-band UVB phototherapy and topical corticosteroids.
  • No recurrence was observed during a 2-year follow-up period.

Implications:

  • This case highlights a rare subtype of pediatric MF with a favorable prognosis.
  • Skin-directed therapies demonstrate efficacy in treating pediatric mycosis fungoides, suggesting a good outlook for similar cases.

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