Sklerosierende Hauterkrankungen

Sticherling M (2019)


Publication Type: Journal article, Review article

Publication year: 2019

Journal

Book Volume: 60

Pages Range: 783-791

Journal Issue: 8

DOI: 10.1007/s00108-019-0643-2

Abstract

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.

Authors with CRIS profile

How to cite

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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