Extensive and deep granulomatous ulcers as an atypical manifestation of cartilage-hair hypoplasia syndrome: A diagnostic and therapeutic challenge

  • Eduardo Rozas-Muñoz*
  • , Rodrigo Blamey-Diaz
  • , Ana Maria Gallardo-Olivos
  • , Javiera Jerez
  • , Juan Andres Madariaga
  • *Autor correspondiente de este trabajo

Producción científica: Contribución a una revistaArtículorevisión exhaustiva

Resumen

Cartilage hypoplasia syndrome is a primary immunodeficiency disease characterized by short stature, hypoplastic hair and a variable degree of immunodeficiency. Noninfectious cutaneous granulomas represent an uncommon yet well-recognized manifestation within the spectrum of primary immunodeficiency diseases. However, cutaneous granulomas as a manifestation of cartilage-hair hypoplasia syndrome, are extremely rare. We present a case of a middle-aged man with cartilage hypoplasia syndrome featuring cutaneous granulomas, manifesting as chronic, extensive and deep cutaneous ulcers. The patient was treated with anti-TNF-alpha adalimumab with partial improvement. Our case underscores the broad spectrum of clinical manifestations associated with cartilage hypoplasia syndrome and adds new evidence to the potential therapeutic efficacy of anti-TNF-alpha drugs in its treatment.

Idioma originalInglés
Páginas (desde-hasta)272-275
Número de páginas4
PublicaciónAustralasian Journal of Dermatology
Volumen65
N.º3
DOI
EstadoPublicada - may. 2024

Nota bibliográfica

Publisher Copyright:
© 2024 Australasian College of Dermatologists.

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