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

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

Abstract

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.

Original languageEnglish
Pages (from-to)272-275
Number of pages4
JournalAustralasian Journal of Dermatology
Volume65
Issue number3
DOIs
StatePublished - May 2024

Bibliographical note

Publisher Copyright:
© 2024 Australasian College of Dermatologists.

Keywords

  • cartilage hair hypoplasia syndrome
  • immunodeficiency
  • ulcers

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