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 capillaroscop...

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Autores principales:	Rosario Foti, Rocco De Pasquale, Ylenia Dal Bosco, Elisa Visalli, Giorgio Amato, Pietro Gangemi, Riccardo Foti, Alice Ramondetta
Formato:	article
Lenguaje:	EN
Publicado:	MDPI AG 2021
Materias:	scleroderma-like sclerodermiform mucinosis scleredema cutaneous sclerosis Medicine (General) R5-920
Acceso en línea:	https://doaj.org/article/711ca30efab048ec8538a1c243f75fbe
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spelling	oai:doaj.org-article:711ca30efab048ec8538a1c243f75fbe2021-11-25T18:19:09ZClinical and Histopathological Features of Scleroderma-like Disorders: An Update10.3390/medicina571112751648-91441010-660Xhttps://doaj.org/article/711ca30efab048ec8538a1c243f75fbe2021-11-01T00:00:00Zhttps://www.mdpi.com/1648-9144/57/11/1275https://doaj.org/toc/1010-660Xhttps://doaj.org/toc/1648-9144Scleroderma-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.Rosario FotiRocco De PasqualeYlenia Dal BoscoElisa VisalliGiorgio AmatoPietro GangemiRiccardo FotiAlice RamondettaMDPI AGarticlescleroderma-likesclerodermiform mucinosisscleredemacutaneous sclerosisMedicine (General)R5-920ENMedicina, Vol 57, Iss 1275, p 1275 (2021)
institution	DOAJ
collection	DOAJ
language	EN
topic	scleroderma-like sclerodermiform mucinosis scleredema cutaneous sclerosis Medicine (General) R5-920
spellingShingle	scleroderma-like sclerodermiform mucinosis scleredema cutaneous sclerosis Medicine (General) R5-920 Rosario Foti Rocco De Pasquale Ylenia Dal Bosco Elisa Visalli Giorgio Amato Pietro Gangemi Riccardo Foti Alice Ramondetta Clinical and Histopathological Features of Scleroderma-like Disorders: An Update
description	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.
format	article
author	Rosario Foti Rocco De Pasquale Ylenia Dal Bosco Elisa Visalli Giorgio Amato Pietro Gangemi Riccardo Foti Alice Ramondetta
author_facet	Rosario Foti Rocco De Pasquale Ylenia Dal Bosco Elisa Visalli Giorgio Amato Pietro Gangemi Riccardo Foti Alice Ramondetta
author_sort	Rosario Foti
title	Clinical and Histopathological Features of Scleroderma-like Disorders: An Update
title_short	Clinical and Histopathological Features of Scleroderma-like Disorders: An Update
title_full	Clinical and Histopathological Features of Scleroderma-like Disorders: An Update
title_fullStr	Clinical and Histopathological Features of Scleroderma-like Disorders: An Update
title_full_unstemmed	Clinical and Histopathological Features of Scleroderma-like Disorders: An Update
title_sort	clinical and histopathological features of scleroderma-like disorders: an update
publisher	MDPI AG
publishDate	2021
url	https://doaj.org/article/711ca30efab048ec8538a1c243f75fbe
work_keys_str_mv	AT rosariofoti clinicalandhistopathologicalfeaturesofsclerodermalikedisordersanupdate AT roccodepasquale clinicalandhistopathologicalfeaturesofsclerodermalikedisordersanupdate AT yleniadalbosco clinicalandhistopathologicalfeaturesofsclerodermalikedisordersanupdate AT elisavisalli clinicalandhistopathologicalfeaturesofsclerodermalikedisordersanupdate AT giorgioamato clinicalandhistopathologicalfeaturesofsclerodermalikedisordersanupdate AT pietrogangemi clinicalandhistopathologicalfeaturesofsclerodermalikedisordersanupdate AT riccardofoti clinicalandhistopathologicalfeaturesofsclerodermalikedisordersanupdate AT aliceramondetta clinicalandhistopathologicalfeaturesofsclerodermalikedisordersanupdate
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Clinical and Histopathological Features of Scleroderma-like Disorders: An Update

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