Systemic sclerosis - a systematic overview: part 1 - disease characteristics and classification, pathophysiologic concepts, and recommendations for diagnosis and surveillance

Vasa. 2011 Jan;40(1):6-19. doi: 10.1024/0301-1526/a000065.

Abstract

Due to its high association with Raynaud's phenomenon systemic sclerosis (SSc) is probably the most common connective tissue disease seen by vascular specialists. In part 1 of our systematic overview we summarize classification concepts of scleroderma disorders, the epidemiologic and genetic burden, the complex pathophysiologic background, and the clinical features and the stage-dependent capillary microscopic features of SSc. Furthermore, we address the diagnostic recommendations propagated by the German Network for Systemic Sclerosis and the Task Force for Diagnosis and Treatment of Pulmonary Hypertension of the European Society of Cardiology, the European Respiratory Society, and the International Society of Heart and Lung Transplantation.

Publication types

  • Review

MeSH terms

  • Capillaries / pathology
  • Capillaries / physiopathology
  • Europe
  • Humans
  • Hypertension, Pulmonary / diagnosis
  • Hypertension, Pulmonary / epidemiology
  • Hypertension, Pulmonary / etiology*
  • Hypertension, Pulmonary / physiopathology
  • Practice Guidelines as Topic
  • Predictive Value of Tests
  • Raynaud Disease / diagnosis
  • Raynaud Disease / epidemiology
  • Raynaud Disease / etiology*
  • Raynaud Disease / physiopathology
  • Risk Factors
  • Scleroderma, Systemic / classification*
  • Scleroderma, Systemic / complications
  • Scleroderma, Systemic / diagnosis
  • Scleroderma, Systemic / epidemiology
  • Scleroderma, Systemic / physiopathology
  • Severity of Illness Index
  • Societies, Medical
  • Terminology as Topic
  • Ulcer / diagnosis
  • Ulcer / epidemiology
  • Ulcer / etiology*
  • Ulcer / physiopathology