Wegener's granulomatosis

Am Fam Physician. 1992 Jan;45(1):191-6.

Abstract

Wegener's granulomatosis is a rare disease of unknown etiology. Until recently it was considered uniformly fatal. Family physicians should be aware of the variable presentations of this disease and keep the diagnosis in mind when faced with a puzzling, chronic, progressive multisystem process. New laboratory markers can lead to earlier diagnosis, and aggressive treatment can improve the prognosis.

Publication types

  • Case Reports
  • Review

MeSH terms

  • Adult
  • Biopsy
  • Clinical Protocols / standards
  • Cyclophosphamide / therapeutic use
  • Diagnosis, Differential
  • Family Practice / methods*
  • Female
  • Granulomatosis with Polyangiitis / diagnosis*
  • Granulomatosis with Polyangiitis / drug therapy
  • Granulomatosis with Polyangiitis / pathology
  • Humans
  • Magnetic Resonance Imaging
  • Prednisone / therapeutic use
  • Tomography, X-Ray Computed
  • Trimethoprim, Sulfamethoxazole Drug Combination / therapeutic use

Substances

  • Trimethoprim, Sulfamethoxazole Drug Combination
  • Cyclophosphamide
  • Prednisone