Clinical characteristics of behçet's disease in palestine, a retrospective cohort study

Abdalrahim Daraghma1, Lamar Baidoun1, Samaa Nazzal1

  • 1Department of Medicine, Faculty of Medicine and Allied Medical Sciences, An-Najah National University, Nablus, Palestine.

BMC Rheumatology
|July 23, 2025
PubMed

Insights

Behçet

Area of Science:

  • Rheumatology
  • Vasculitis Research
  • Systemic Inflammatory Diseases

Background:

  • Behçet's Disease (BD) is a chronic, systemic vasculitis with unknown cause.
  • It presents with recurrent ulcers, ocular, vascular, and other organ involvement.
  • Diagnosis relies on clinical criteria, lacking specific lab tests.

Purpose of the Study:

  • To describe the prevalence and characteristics of Behçet's Disease in Palestine.
  • To provide insights into disease patterns for improved diagnosis and management.

Main Methods:

  • Retrospective cohort study of 60 BD patients in the West Bank and Jerusalem.
  • Diagnosis confirmed using International Criteria for Behçet's Disease (ICBD).
  • Data collected via chart review and interviews; complications assessed using BODI.

Main Results:

  • Most common initial symptoms: oral ulcers (96.7%), genital ulcers (86.7%), ocular lesions (66.7%).
  • Frequent complications included vascular events (36.7%) and skin ulcerations (33.3%).
  • Neurological manifestations (25%) and pathergy test (18.3%) were less common.

Conclusions:

  • Oral and genital ulcers are the most common BD manifestations in Palestine.
  • Vascular events and visual impairment are frequent complications.
  • BD characteristics showed no significant gender difference in this cohort.
Abstract

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