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A young woman with late-stage Vogt-Koyanagi-Harada disease was successfully treated at a hospital.

Cyclosporine-A can cause serious blood clots in the brain, so patients need careful monitoring.

Blood vessel patterns in skin diseases relate to certain blood markers in systemic sclerosis but not in psoriasis or psoriatic arthritis, and may indicate circulation issues in alopecia.

Early diagnosis and treatment of Kaposi varicelliform eruption are crucial to prevent severe complications.

A new mutation in the STING protein causes a disease with lupus-like symptoms and responds well to a specific inhibitor treatment.

Genetic marker rs12558842 strongly linked to male hair loss.

Renal histology is crucial for diagnosing simultaneous SLE and IgG4RD.

Understanding cellular interactions in VCA may lead to better treatments and reduce rejection.

Anti-phospholipid antibodies in SLE can cause thrombosis and bone necrosis.

Mixed Connective Tissue Disease can develop from overlapping symptoms of several autoimmune diseases, making diagnosis complex.

Digital gangrene can be an unusual first sign of late-onset lupus.

Visceral leishmaniasis can mimic rheumatoid arthritis symptoms, especially in immunocompromised patients.

A woman with skin and joint issues progressed from one type of lupus to another, highlighting the need to recognize complex conditions.

SLE can cause unusual gastrointestinal symptoms, and immunosuppressive therapy can be effective.

The woman's facial symptoms are best explained by primary Sjögren’s Syndrome.

A black-skinned woman was diagnosed with Vogt-Koyanagi-Harada disease and treated with steroids and eye drops.

IV cyclophosphamide effectively treated severe lupus nephritis in Indian patients, but longer follow-up is needed.

The patient improved after antiviral treatment for a viral infection.

A man developed autoimmune symptoms after the Pfizer COVID-19 vaccine, highlighting the need for thorough vaccine safety checks.

Systemic lupus erythematosus treatment can restore vision in patients with retinal artery occlusion.

BIVV009 is a safe treatment for bullous pemphigoid that reduces C3 deposition without harmful side effects.

Correct diagnosis is crucial for treating overlapping conditions like NMOSD and SLE effectively.

The case shows how hard it is to tell apart Multiple Autoimmune Syndrome from other similar autoimmune conditions, but correct diagnosis is key for treatment to work.

Consider infectious diseases like visceral leishmaniasis before diagnosing autoimmune hepatitis.

Vasodilators may worsen abdominal aortic aneurysm.

A patient with Ivemark syndrome developed mixed type vitiligo after a hepatitis C infection, showing different treatment responses and immune cell involvement in the skin.

Different rheumatological diseases can cause specific skin problems.

Early treatment of pediatric lupus-related eye issues is crucial to prevent vision loss.