How do you know if you have primary or secondary sjogrens?

Primary Sjögren syndrome occurs in the absence of another underlying rheumatic disorder
rheumatic disorder
Rheumatism or rheumatic disorders are conditions causing chronic, often intermittent pain affecting the joints or connective tissue.
https://en.wikipedia.orgwiki › Rheumatism
, whereas secondary Sjögren syndrome is associated with another underlying rheumatic disease, such as systemic lupus erythematosus (SLE), rheumatoid arthritis (RA), or scleroderma.
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How do I know if I have primary Sjogren's syndrome?

Diagnosis and Tests

Blood tests: These tests detect specific antibodies in the blood. They look for anti-nuclear antibodies (ANA), anti-Sjögren's syndrome antibodies (anti-SSA, also called anti-Ro) and anti-Sjögren's syndrome type B (anti-SSB, also called anti-La).
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Which is worse primary or secondary Sjogren's?

SSc appears to be less severe in patients with SS-SSc than SSc alone with a lower frequency of lung fibrosis (P = 0.05). Compared with patients with pSS or SSc alone, SS-SSc patients were more likely to have another autoimmune disorder and other autoantibodies (SS-SSc vs pSS, P = 0.02 and P = 0.03, respectively).
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What are the symptoms of secondary Sjogren's syndrome?

The main symptoms of both primary and secondary Sjögren's syndrome include:
  • Dryness of the eyes, mouth, throat, and upper airways.
  • Problems with swallowing food and medication.
  • Changes in sense of taste.
  • Chronic cough.
  • Hoarseness.
  • Dental problems.
  • Difficulty speaking.
  • Vaginal dryness.
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What is secondary Sjogren's syndrome?

Secondary Sjögren's syndrome is generally diagnosed when someone with an established autoimmune disease, such as rheumatoid arthritis or lupus, develops extreme dryness of the eyes and mouth. This diagnosis only rarely requires a lip biopsy.
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Sjogren’s Syndrome ("Dry Eye Syndrome") | Primary vs. Secondary, Symptoms, Diagnosis and Treatment



What is primary Sjögren syndrome?

Primary Sjogren syndrome is an autoimmune condition in which dry eyes (keratoconjunctivitis sicca) and dry mouth (xerostomia) result from lymphocytic infiltration of lacrimal and salivary glands.
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What drugs make sjogrens worse?

Avoid medicines that are known to cause dry eyes. These include antihistamines, diuretics, and some antidepressants. Talk with your doctor if you take any of these medicines. Sometimes the benefits of a medicine outweigh the risks.
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What mimics Sjogren's syndrome?

Certain diseases affecting salivary and lacrimal glands such as sarcoidosis, IgG4-related disease, chronic hepatitis C virus, HIV infections, and graft-versus-host disease can mimic Sjögren's syndrome, usually via a process of similar inflammation of affected glands.
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What does a sjogrens flare feel like?

Joint pain is one of the most common symptoms of Sjögren's syndrome. Multiple joints are painful, usually episodically with periods of joint pain, known as “flares”, followed by periods of little or no joint pain. Tenderness and swelling of the joints, when present, are indicative of inflammatory arthritis.
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What does Sjogren's pain feel like?

Your joints may be painful and swollen due to inflammation, or you might feel that various parts of your body, such as your muscles, are achy and tender. Some people with this condition have headaches and migraines.
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Does having Sjogren's mean you are immunocompromised?

As a note – not all Sjögren's patients have compromised immune systems. This specific risk factor is for those who regularly take drugs to suppress the immune system.
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What is the difference between Sjogren's A and B?

SS-A antibodies are found in approximately 60-80% of Sjögren's syndrome patients. SS-B antibodies are less common, being found in approximately 30-50% of Sjögren's syndrome patients. SS-A antibodies thus occur commonly by themselves. However, it is very uncommon for SS-B antibodies to occur alone.
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Is Sjogren's syndrome worse than lupus?

The prognosis with SS is generally better than that of other autoimmune diseases such as lupus. Patients with just exocrine gland involvement do not appear to have increased mortality.
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What does Sjögren's fatigue feel like?

Sjogren's Syndrome patients often complain of mental fatigue or “brain fog.” Brain fog impairs focus, causes fuzzy concentration, and contributes to difficulty in problem-solving.
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What does Sjogren's tongue look like?

a smooth, red tongue. a change in how food tastes. dry, sore and cracked skin at the corners of your lips. problems such as tooth decay, gum disease, mouth ulcers, and oral thrush (a fungal infection that can cause a raw, red or white tongue)
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What triggers a Sjogren's flare?

Autoimmune diseases such as Sjogren's syndrome are highly likely to be triggered by environmental factors such as pollution, infections, certain medications, diet, and allergy-causing agents. Make a note of potential environmental triggers, and try to steer clear of them as much as possible.
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What vitamins help Sjogren's?

Herbs and Supplements for Sjogren's syndrome
  • Cysteine.
  • Evening Primrose.
  • Gamma-Linolenic Acid (GLA)
  • Omega-6 Fatty Acids.
  • Sulfur.
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What does Plaquenil do for sjogrens?

Immunosuppressive Medications

These medications work by curbing an overactive immune system, thereby decreasing inflammation. Your doctor may prescribe a mild medication first, such as hydroxychloroquine, sold as Plaquenil®.
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How do you stop Sjogren's progression?

Eat well and often. Eating an anti-inflammatory diet is one of the ways to reduce Sjogren's syndrome flares and provide adequate nutrition, thereby reducing fatigue. Ensure that your diet consists of food with high fiber, healthy fats, and spices such as garlic, ginger, and turmeric.
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Can Sjogren's be misdiagnosed?

Sjogren's syndrome is a condition that is important for all health professionals to research and understand. This syndrome and its symptoms are known to be misdiagnosed with diseases such as diabetes, lupus, rheumatoid arthritis, fibromyalgia, chronic fatigue syndrome, and multiple sclerosis.
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What are the differential diagnosis for Sjogren's syndrome?

The differential diagnosis of SS includes conditions and medications that can produce keratoconjunctivitis sicca, xerostomia, and parotid gland enlargement. Xerostomia may be caused by amyloidosis, diabetes mellitus, sarcoidosis, SS, viral infections, trauma, or irradiation or may be psychogenic.
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Does Sjogren's always show up in blood test?

Diagnosing Sjögren's syndrome requires gathering a lot of information, which your doctors will collect from a combination of tests on your eyes and mouth, blood and urine tests, and biopsies.
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Should you get the Covid vaccine if you have Sjogren's syndrome?

As a person with Sjögren's, should I receive a vaccination for COVID-19? Yes. We recommend that all people with Sjögren's should be vaccinated, with the exception of children under the age of 16 (since children were not included in the trials that led to the EUA for the Pfizer and Moderna vaccines).
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How does a rheumatologist treat Sjogren's syndrome?

There is no cure or specific treatment for Sjogren's syndrome. For patients with mild disease, symptom-orientated treatments may be used such as: Artificial tears. Chewing sugarless gum to stimulate the secretion of saliva.
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Does sjogrens get worse over time?

Symptoms are mild in most people but can be very severe in others. Symptoms can vary over time and may improve, worsen, or even go away completely for periods.
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