Secondary Sjögren syndrome (Q44391): Difference between revisions

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Síndrome de Sjögren secundária é uma doença autoimune inflamatória progressiva que afeta as glândulas exócrinas na presença de outras doenças autoimunes sistêmicas, como artrite reumatoide, lúpus eritematoso sistêmico e esclerose sistêmica. Os infiltrados linfocíticos substituem o epitélio funcional, levando ao ressecamento oral e ocular.
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Secondary Sjögren syndrome is a progressive inflammatory autoimmune disease affecting the exocrine glands in the presence of other systemic autoimmune diseases, such as rheumatoid arthritis, systemic lupus erythematosus, and systemic sclerosis. Lymphocytic infiltrates replace functional epithelium, leading to oral and ocular dryness.

Revision as of 11:50, 13 August 2026

Secondary Sjögren syndrome is a progressive inflammatory autoimmune disease affecting the exocrine glands in the presence of other systemic autoimmune diseases, such as rheumatoid arthritis, systemic lupus erythematosus, and systemic sclerosis. Lymphocytic infiltrates replace functional epithelium, leading to oral and ocular dryness.
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4A43.21
    English
    Secondary Sjögren syndrome
    Secondary Sjögren syndrome is a progressive inflammatory autoimmune disease affecting the exocrine glands in the presence of other systemic autoimmune diseases, such as rheumatoid arthritis, systemic lupus erythematosus, and systemic sclerosis. Lymphocytic infiltrates replace functional epithelium, leading to oral and ocular dryness.

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