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Sjögren's Syndrome

Diagnosis, symptoms, and treatment modalities.

General Information on Sjögren's Syndrome

Sjögren's syndrome is a chronic systemic autoimmune disease characterized by the immune system erroneously infiltrating and destroying the body's moisture-producing exocrine glands, predominantly the lacrimal (tear) and salivary glands. This lymphocytic infiltration causes severe ocular and oral dryness. In our Rheumatology outpatient clinics, diagnosis is confirmed via specific autoantibody testing and minor salivary gland (labial) biopsy. The condition is managed holistically using artificial tears, secretagogue agents (to stimulate saliva), and systemic immunosuppressive pharmacotherapy.

Disease Details and Frequently Asked Questions

Detailed clinical information regarding the pathology can be accessed under the following headings.
What is Sjögren's Syndrome?

It is a systemic rheumatic disorder wherein the body's defensive immune mechanism becomes dysregulated and mounts an autoimmune attack against its own 'exocrine glands'—the glands responsible for producing tears, saliva, and vaginal secretions—leading to their progressive destruction.

What is the difference between Primary and Secondary Sjögren's?

Primary Sjögren's: The condition manifests independently, without the presence of any other underlying rheumatic disease.
Secondary Sjögren's: The syndrome develops concomitantly with another established autoimmune disease, such as Rheumatoid Arthritis or Systemic Lupus Erythematosus (SLE).

What are the core symptoms (Xerophthalmia and Xerostomia)?

Patients experience a persistent sensation of grit or sand in the eyes accompanied by burning and severe redness (xerophthalmia). Orally, the dryness (xerostomia) is so profound that swallowing dry food without liquid assistance becomes nearly impossible, accompanied by a fissured tongue and a drastically increased incidence of dental caries. Cutaneous and vaginal dryness are also highly prevalent.

Does it involve the joints or internal organs?

Yes, as it is a systemic disease. Beyond glandular involvement, it can cause significant inflammatory arthritis (joint swelling and arthralgia). Extraglandular manifestations may also include interstitial lung disease (pulmonary fibrosis), renal tubular dysfunction, profound fatigue, and generalized myalgia.

How is it diagnosed?

Clinical suspicion is supported by the Schirmer's Test, which objectively measures tear production, and serological detection of specific autoantibodies, primarily Anti-Ro (SSA) and Anti-La (SSB). Definitive histological diagnosis is established via a minor salivary gland biopsy taken from the inner lower lip, demonstrating characteristic focal lymphocytic infiltration.

What are the therapeutic protocols?

There is no curative treatment capable of regenerating the destroyed glandular tissue. Symptomatic relief is achieved through the continuous application of preservative-free artificial tear drops and cholinergic agonists (e.g., Pilocarpine) to stimulate residual salivary flow. For systemic joint or organ involvement, Rheumatological immunomodulatory agents (such as Hydroxychloroquine) and corticosteroids are prescribed.

Our health library contents are prepared for informational purposes only and with scientific data available at the time of recording. For all your questions, concerns, diagnosis, or treatment regarding your health, please consult your doctor or a healthcare institution.


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