Immunologic and nonimmunologic sclerodermal skin conditions - review
- PMID: 37600771
- PMCID: PMC10432860
- DOI: 10.3389/fimmu.2023.1180221
Immunologic and nonimmunologic sclerodermal skin conditions - review
Abstract
Scleroderma-like cutaneous lesions have been found in many pathological conditions and they have the clinical appearance of sclerotic or scleroatrophic lesions. Affected skin biopsies described histopathological changes similar to those of scleroderma located strictly on the skin or those of systemic sclerosis. These skin lesions can be found in inflammatory diseases with autoimmune substrate (generalized morphea, chronic graft versus host disease, eosinophilic fasciitis), tissue storage diseases (scleredema, scleromyxedema, nephrogenyc systemic fibrosis, systemic amyloidosis), metabolic diseases (porphyrya cutanea tarda, phenylketonuria, hypothyroidism, scleredema diabeticorum), progeroid syndromes. Given the multiple etiologies of sclerodermal lesions, a correct differential diagnosis is necessary to establish the appropriate treatment.
Keywords: immunological skin conditions; lichen sclerosus (balanitis xerotica obliterans); scleredema Burschke; scleroatrophic lichen; scleromyxedema; systemic sclerosis.
Copyright © 2023 Bobeica, Niculet, Craescu, Parapiru, Corduneanu-Luca, Debita, Pelin, Tiutiuca, Vasile, Nicolescu, Miulescu, Balan and Tatu.
Conflict of interest statement
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
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