Purpura syndromes

Author:Prof. Dr. med. Peter Altmeyer

All authors of this article

Last updated on: 11.04.2024

Dieser Artikel auf Deutsch

Requires free registration (medical professionals only)

Please login to access all articles, images, and functions.

Our content is available exclusively to medical professionals. If you have already registered, please login. If you haven't, you can register for free (medical professionals only).


Requires free registration (medical professionals only)

Please complete your registration to access all articles and images.

To gain access, you must complete your registration. You either haven't confirmed your e-mail address or we still need proof that you are a member of the medical profession.

Finish your registration now

DefinitionThis section has been translated automatically.

"Purpura" refers to a polyetiological clinical picture characterized by haemorrhages of the skin.

The onset of purpura can be acute or chronic and insidious.

Purpura can be localized or disseminated, small spots or extensive.

A single purpura lesion can be flat (spot) or elevated (papule/plaque = palpable purpura), inflammatory (vasculitis) or non-inflammatory (e.g. due to a vasculopathy).

In a broader sense, independent diseases are also referred to as "purpura", which are associated with bleeding into the skin (e.g. purpura pigmentosa progressiva; purpura Schönlein-Henoch).

ClassificationThis section has been translated automatically.

DiagnosticsThis section has been translated automatically.

The "dermatological signal" purpura, requires further diagnostic clarification by laboratory values and gfls. by a skin biopsy.

Authors

Last updated on: 11.04.2024