Rare Diseases Symptoms Automatic Extraction

Wegener's granulomatosis: a new entity in the growing differential diagnosis of Degos' disease.

[malignant atrophic papulosis]

Wegener's granulomatosis (WG) is a multisystemic vasculitis, with skin involvement in 14% of cases and with palpable purpura, subcutaneous nodules and necrotic papules as the common features.(1) We present a patient diagnosed with WG who had multiple whitish papules similar to those of malignant atrophic papulosis (Degos' disease), which appeared during a flare of his disease. Lesions of malignant atrophic papulosis are said to be pathognomonic; nevertheless, various diseases with similar clinical lesions have been described. To our knowledge, this is the first reported case of such lesions in a patient with WG, and we suggest WG should be included in the differential diagnosis of Degos' disease.

Diseases presenting "purpura" symptom

  • esophageal adenocarcinoma
  • familial mediterranean fever
  • heparin-induced thrombocytopenia
  • hodgkin lymphoma, classical
  • inclusion body myositis
  • malignant atrophic papulosis
  • omenn syndrome
  • severe combined immunodeficiency
  • systemic capillary leak syndrome
  • typhoid

This symptom has already been validated