[Inaugural symptoms of Horton's disease in a series of 260 patients]

C Becourt-Verlomme1, R Barouky, C Alexandre

  • 1Service de médecine interne, hôpital Lyon-Sud, 69495 Pierre-Bénite, France.

La Revue De Medecine Interne
|August 18, 2001
PubMed

Insights

Giant cell arteritis, or Horton disease, often presents with atypical symptoms. Recognizing these, such as cough or arthritis, is crucial for timely diagnosis and treatment with corticosteroids.

Area of Science:

  • Rheumatology
  • Internal Medicine
  • Geriatrics

Context:

  • Horton disease (giant cell arteritis) diagnosis can be challenging due to atypical presentations.
  • A retrospective review of 260 patient files from 1979-1999 across internal medicine, rheumatology, and geriatric departments was conducted.

Purpose:

  • To highlight the diagnostic challenges posed by atypical signs and symptoms of Horton disease.
  • To emphasize the importance of recognizing less common manifestations for prompt diagnosis.

Summary:

  • The study analyzed 260 Horton disease cases, predominantly affecting females aged 75.
  • Atypical symptoms included neurological (4 patients), cutaneous (5 patients), and renal (2 patients) manifestations.
  • Cough (21 cases) and peripheral arthritis (9 cases) were frequent, with positive temporal artery biopsies in 57% and 70% respectively, responding to corticosteroids and NSAIDs.

Impact:

  • Increased awareness of atypical Horton disease symptoms can improve diagnostic accuracy.
  • Early diagnosis and initiation of corticosteroid therapy are vital for managing giant cell arteritis.
  • This research aids clinicians in identifying and treating patients with less common presentations of Horton disease.
Abstract

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