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Lymphomatoid Papulosis Type D in a Mestizo-Ancestry Man
Sofía Saraí Villegas-González1, Nadia Gómez2, Mario Magaña1
1Service of Dermatology, Hospital General de México "Dr. Eduardo Liceaga," S.S./School of Medicine, Universidad Nacional Autónoma de México, Mexico City, Mexico; and.
This case study details a rare Type D Lymphomatoid Papulosis (LyP) in a mestizo patient. The findings highlight the diagnostic challenges and good prognosis of this CD30+ cutaneous lymphoproliferative disorder.
Area of Science:
- Dermatology
- Oncology
- Pathology
Background:
- Lymphomatoid papulosis (LyP) is a CD30+ cutaneous lymphoproliferative disorder.
- It presents as a chronic, recurrent, self-healing eruption with T-cell lymphoma features.
- Type D LyP is characterized by epidermotropism of atypical CD8+ and CD30+ lymphocytes, posing diagnostic challenges.
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