Journal article

Systemic sclerosis -: a challenge in rheumatology


Authors listSaar, P.; Mueller-Ladner, U.

Publication year2006

Pages429-438

JournalZeitschrift für Rheumatologie

Volume number65

Issue number5

ISSN0340-1855

eISSN1435-1250

DOI Linkhttps://doi.org/10.1007/s00393-006-0076-x

PublisherSpringer


Abstract
The connective tissue disease systemic sclerosis (SSc is still a challenge to every rheumatologist. SSc is characterized by progressing fibrosis of the skin and internal organs, abnormal activation of the immune system and distinct changes in microcirculation. Although it is a rare disease with a prevalence of about 20:100,000, one may come across it in daily practice. SSc is classified into limited and diffuse forms. Both entities usually involve internal organs. Life expectancy is limited and depends predominantly on the extent of the organs involved. Therefore, it is essential to diagnose and to identify and closely monitor the organs involved.



Citation Styles

Harvard Citation styleSaar, P. and Mueller-Ladner, U. (2006) Systemic sclerosis -: a challenge in rheumatology, Zeitschrift für Rheumatologie, 65(5), pp. 429-438. https://doi.org/10.1007/s00393-006-0076-x

APA Citation styleSaar, P., & Mueller-Ladner, U. (2006). Systemic sclerosis -: a challenge in rheumatology. Zeitschrift für Rheumatologie. 65(5), 429-438. https://doi.org/10.1007/s00393-006-0076-x



Keywords


Connective tissue diseaseFIBROSISORGAN INVOLVEMENTsystemic sclerosis (SSc)

Last updated on 2025-02-04 at 03:50