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] |
---|
Links: |
doi.org [kostenfrei] |
---|
Themen: |
Cutaneous sclerosis |
---|
doi: |
10.3390/medicina57111275 |
---|
funding: |
|
---|---|
Förderinstitution / Projekttitel: |
|
PPN (Katalog-ID): |
DOAJ047389141 |
---|
LEADER | 01000caa a22002652 4500 | ||
---|---|---|---|
001 | DOAJ047389141 | ||
003 | DE-627 | ||
005 | 20240412131753.0 | ||
007 | cr uuu---uuuuu | ||
008 | 230227s2021 xx |||||o 00| ||eng c | ||
024 | 7 | |a 10.3390/medicina57111275 |2 doi | |
035 | |a (DE-627)DOAJ047389141 | ||
035 | |a (DE-599)DOAJ711ca30efab048ec8538a1c243f75fbe | ||
040 | |a DE-627 |b ger |c DE-627 |e rakwb | ||
041 | |a eng | ||
050 | 0 | |a R5-920 | |
100 | 0 | |a Rosario Foti |e verfasserin |4 aut | |
245 | 1 | 0 | |a Clinical and Histopathological Features of Scleroderma-like Disorders: An Update |
264 | 1 | |c 2021 | |
336 | |a Text |b txt |2 rdacontent | ||
337 | |a Computermedien |b c |2 rdamedia | ||
338 | |a Online-Ressource |b cr |2 rdacarrier | ||
520 | |a 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. | ||
650 | 4 | |a scleroderma-like | |
650 | 4 | |a sclerodermiform mucinosis | |
650 | 4 | |a scleredema | |
650 | 4 | |a cutaneous sclerosis | |
653 | 0 | |a Medicine (General) | |
700 | 0 | |a Rocco De Pasquale |e verfasserin |4 aut | |
700 | 0 | |a Ylenia Dal Bosco |e verfasserin |4 aut | |
700 | 0 | |a Elisa Visalli |e verfasserin |4 aut | |
700 | 0 | |a Giorgio Amato |e verfasserin |4 aut | |
700 | 0 | |a Pietro Gangemi |e verfasserin |4 aut | |
700 | 0 | |a Riccardo Foti |e verfasserin |4 aut | |
700 | 0 | |a Alice Ramondetta |e verfasserin |4 aut | |
773 | 0 | 8 | |i In |t Medicina |d MDPI AG, 2016 |g 57(2021), 11, p 1275 |w (DE-627)DOAJ000119180 |x 16489144 |7 nnns |
773 | 1 | 8 | |g volume:57 |g year:2021 |g number:11, p 1275 |
856 | 4 | 0 | |u https://doi.org/10.3390/medicina57111275 |z kostenfrei |
856 | 4 | 0 | |u https://doaj.org/article/711ca30efab048ec8538a1c243f75fbe |z kostenfrei |
856 | 4 | 0 | |u https://www.mdpi.com/1648-9144/57/11/1275 |z kostenfrei |
856 | 4 | 2 | |u https://doaj.org/toc/1010-660X |y Journal toc |z kostenfrei |
856 | 4 | 2 | |u https://doaj.org/toc/1648-9144 |y Journal toc |z kostenfrei |
912 | |a GBV_USEFLAG_A | ||
912 | |a GBV_DOAJ | ||
951 | |a AR | ||
952 | |d 57 |j 2021 |e 11, p 1275 |