Sjögren syndrome (Q44393): Difference between revisions
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A síndrome de Sjögren (SS) é uma doença autoimune inflamatória sistêmica lentamente progressiva, que afeta primariamente as glândulas exócrinas. Os infiltrados linfocíticos substituem o epitélio funcional, levando ao ressecamento oral e ocular. Autoanticorpos característicos (por exemplo, anti-Ro/SS-A e/ou anti-La/SS-B) são produzidos. O distúrbio pode ocorrer isolado (é então conhecido como "SS primária") ou em associação com outra doença autoimune (é então conhecido como "SS secundária"). | |||
| description / en | description / en | ||
Sjögren syndrome (SS) is a slowly progressive, systemic inflammatory autoimmune disease affecting primarily the exocrine glands. Lymphocytic infiltrates replace functional epithelium, leading to oral and ocular dryness. Characteristic autoantibodies (e.g., anti-Ro/SS-A and/or anti-La/SS-B) are produced. The disorder can occur alone (it is then known as “primary SS”) or in association with another autoimmune disease (it is then known as “secondary SS”). | |||
Revision as of 11:50, 13 August 2026
Sjögren syndrome (SS) is a slowly progressive, systemic inflammatory autoimmune disease affecting primarily the exocrine glands. Lymphocytic infiltrates replace functional epithelium, leading to oral and ocular dryness. Characteristic autoantibodies (e.g., anti-Ro/SS-A and/or anti-La/SS-B) are produced. The disorder can occur alone (it is then known as “primary SS”) or in association with another autoimmune disease (it is then known as “secondary SS”).
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | 4A43.2 |
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| English | Sjögren syndrome |
Sjögren syndrome (SS) is a slowly progressive, systemic inflammatory autoimmune disease affecting primarily the exocrine glands. Lymphocytic infiltrates replace functional epithelium, leading to oral and ocular dryness. Characteristic autoantibodies (e.g., anti-Ro/SS-A and/or anti-La/SS-B) are produced. The disorder can occur alone (it is then known as “primary SS”) or in association with another autoimmune disease (it is then known as “secondary SS”). |
