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 "vasculitis" symptom

  • coats disease
  • dracunculiasis
  • dystrophic epidermolysis bullosa
  • erdheim-chester disease
  • erythropoietic protoporphyria
  • familial mediterranean fever
  • focal myositis
  • inclusion body myositis
  • malignant atrophic papulosis
  • papillon-lefèvre syndrome
  • pyruvate dehydrogenase deficiency
  • scrub typhus
  • sneddon syndrome
  • typhoid
  • waldenström macroglobulinemia

This symptom has already been validated