Clinical and Histopathological Features of Scleroderma-like Disorders: An Update

Scleroderma-like disorders include a set of entities involving cutis, subcutis and, sometimes, even muscular tissue, caused by several pathogenetic mechanisms responsible for different clinical–pathological pictures. The absence of antinuclear antibodies (ANA), Raynaud’s phenomenon and capillaroscopic anomalies constitutes an important element of differential diagnosis with systemic sclerosis. When scleroderma can be excluded, on the basis of the main body sites, clinical evolution, any associated pathological conditions and specific histological features, it is possible to make a correct diagnosis..

Medienart:

E-Artikel

Erscheinungsjahr:

2021

Erschienen:

2021

Enthalten in:

Zur Gesamtaufnahme - volume:57

Enthalten in:

Medicina - 57(2021), 11, p 1275

Sprache:

Englisch

Beteiligte Personen:

Rosario Foti [VerfasserIn]
Rocco De Pasquale [VerfasserIn]
Ylenia Dal Bosco [VerfasserIn]
Elisa Visalli [VerfasserIn]
Giorgio Amato [VerfasserIn]
Pietro Gangemi [VerfasserIn]
Riccardo Foti [VerfasserIn]
Alice Ramondetta [VerfasserIn]

Links:

doi.org [kostenfrei]
doaj.org [kostenfrei]
www.mdpi.com [kostenfrei]
Journal toc [kostenfrei]
Journal toc [kostenfrei]

Themen:

Cutaneous sclerosis
Medicine (General)
Scleredema
Scleroderma-like
Sclerodermiform mucinosis

doi:

10.3390/medicina57111275

funding:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

DOAJ047389141