Sclerosing conditions of the skin are manifested by a full spectrum of presentations that includes skin-limited forms as well as those which can involve internal organs and result in death. At this point, we are just beginning to understand the mechanisms of tissue fibrosis, and it is likely that the fibrotic processes are a heterogeneous group of disorders in which perturbation of multiple molecular pathways, including vascular and immunologically mediated pathways, can lead to fibrosis. We now have some moderately effective therapies for vascular aspects of systemic sclerosis (eg, bosentan for pulmonary arterial hypertension, calcium-channel blockers for Raynaud's, or angiotensin-converting enzyme inhibitors for renal crisis). We also are beginning to find treatments interrupting the immunologic pathways that manifest as systemic sclerosis (eg, methotrexate for the skin or cyclophosphamide for the lungs). The basic process of fibrosis, however, awaits proven, effective therapy. (copyright) 2006 Elsevier Inc. All rights reserved.
CITATION STYLE
Grechneva, E. V., & Sharonova, Yu. V. (2022). SYSTEMIC AND LOCALIZED SCLERODERMA. Научное Обозрение. Биологические Науки (Scientific Review. Biological Sciences), (№2 2022), 43–47. https://doi.org/10.17513/srbs.1271
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