Sticherling M (2019)
Publication Type: Journal article, Review article
Publication year: 2019
Book Volume: 60
Pages Range: 783-791
Journal Issue: 8
DOI: 10.1007/s00108-019-0643-2
Sclerosing skin manifestations are more a symptom than a diagnosis and must therefore be meticulously clarified. Systemic scleroderma as a multiorgan disease must be distinguished from localized scleroderma or morphea because in addition to a different clinical picture they have a different prognosis and necessitate other therapeutic procedures. Rare sclerosing skin diseases with implications for internal medicine are eosinophilic fasciitis, Buschke’s scleredema adultorum, scleromyxedema and nephrogenic systemic fibrosis.
APA:
Sticherling, M. (2019). Sklerosierende Hauterkrankungen. Internist, 60(8), 783-791. https://doi.org/10.1007/s00108-019-0643-2
MLA:
Sticherling, Michael. "Sklerosierende Hauterkrankungen." Internist 60.8 (2019): 783-791.
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