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Dtsch Med Wochenschr 2018; 143(23): 1690-1699
DOI: 10.1055/a-0569-3822
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© Georg Thieme Verlag KG Stuttgart · New York

Hautveränderungen als Schlüssel zur Diagnose systemischer Erkrankungen

Dermal Clues to Systemic Diseases
Thomas Mettang
,
Markus Streit
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Publication History

Publication Date:
15 November 2018 (online)

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Abstract

Many systemic diseases go along with dermal involvement. Only a few of systemic diseases show characteristic skin derangements directly leading to the diagnosis of the underlying disease. Ten of these entities are described within this article. Some of these are autoimmune diseases, such as systemic lupus erythematodes, dermatomyositis or the anti-synthetase-syndrome. Others are genetic diseases with benign or malignant neoplasias (Peutz-Jeghers-syndrome, neurofibromatosis, tuberous sclerosis, Birt-Hogg-Dubé-syndrome, Cowden-syndrome). Other genetically based diseases with typical skin manifestations are characterised by vascular malformations (Pseudoxanthoma elasticum and Osler-Weber-Rendu syndrome) or metabolic and structural organ defects (Morbus Fabry, cystic fibrosis). Being familiar with the typical skin-appearance of these diseases will allow physicians and general practitioners to make a timely diagnosis.

Die meisten krankhaften Hautveränderungen betreffen nur die Haut selbst. Gelegentlich allerdings zeigt die Haut auch bei nicht primär dermatologischen Erkrankungen mehr oder weniger ausgeprägte Symptome. Einige davon sind so typisch, dass sie als eigentlicher diagnostischer Schlüssel betrachtet werden können. Dieser Beitrag stellt zehn solcher Hautveränderungen vor, die auch für Internisten und Allgemeinmediziner bedeutsam sind.

Schlüsselwörter

Hautveränderungen - Blickdiagnose - systemische Erkrankungen - genetische Erkrankungen - Differenzialdiagnose

Key words

dermatological disease - skin disease - systemic disease - diagnosis
 

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