Rare Diseases Symptoms Automatic Extraction

A fatal case of Degos' disease which presented with recurrent intestinal perforation.

[malignant atrophic papulosis]

Degos' disease, otherwise known as "malignant atrophic papulosis" is a rare vasculopathy with an unknown etiology characterized by typical cutaneous lesions. Involvement of the gastrointestinal (GI) tract is observed in approximately half of patients and small infarctions in the mucosa can cause perforation and resulting peritonitis, the leading cause of death. We present a fatal case of Degos' disease with skin and GI involvement, manifesting as recurrent intestinal perforations and peritonitis, in a 15-year-old Iranian boy.

Diseases presenting "approximately half" symptom

  • benign recurrent intrahepatic cholestasis
  • classical phenylketonuria
  • epidermolysis bullosa simplex
  • erdheim-chester disease
  • hirschsprung disease
  • malignant atrophic papulosis

You can validate or delete this automatically detected symptom