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Hepatitis B vaccination can trigger HSP, and vitamin D correction and tonsillectomy can effectively manage it.

A rare type of skin lymphoma was identified, affecting hair follicles and sweat glands.

Early detection and treatment of primary biliary cirrhosis and related autoimmune diseases improve outcomes.

Inflammation may cause nail issues in Cronkhite–Canada Syndrome.

A man developed facial skin lesions after a stem cell transplant, which improved with specific treatments.

A baby was diagnosed with IFAP syndrome due to a new genetic mutation, showing severe skin and developmental issues.

Interface dermatitis is the most common skin change in drug-induced hypersensitivity syndrome.

Cronkhite-Canada syndrome is a rare condition causing gut polyps, hair loss, skin changes, and nail issues, often with a poor outlook.

Oral isotretinoin temporarily improved skin symptoms in a child with IFAP syndrome.

Tofacitinib effectively treated a woman's complex autoimmune and autoinflammatory disorders.

ECCL should be considered in patients with specific skin and eye lesions.

A 5-year-old boy's skin condition improved with systemic valganciclovir after a cardiac transplant and immunosuppressive therapy.

A TNFAIP3 gene mutation can cause unusual and varied symptoms of lupus and Sjogren's syndrome.

Purpura fulminans can signal underlying autoimmune disorders, not just infections.

A 15-year-old with KID syndrome developed a rare skin condition called PEHFN.

PI3Kδ inhibition may effectively treat cutaneous chronic graft-versus-host disease.

Transplant patients often get skin problems, with treatments varying by condition.

Enteral supplements can improve symptoms of Cronkhite-Canada syndrome.

Some patients may experience temporary total hair loss from hepatitis C treatment with PEG-interferon and ribavirin.

People with mycosis fungoides/Sézary syndrome have a much lower quality of life.

A 70-year-old woman with a rare skin condition improved after treatment with topical steroids and acitretin.

Early diagnosis and treatment with corticosteroids can improve outcomes in Cronkhite–Canada syndrome.

An 8-year-old Saudi boy was diagnosed with a rare genetic disorder causing hair loss, skin issues, and light sensitivity.

The man's symptoms improved after treating his scurvy with high-dose vitamin C.

The patient improved after antiviral treatment for a viral infection.

A Chinese man with KID syndrome had a new mutation in the GJB2 gene.

Leflunomide successfully treated a rare skin condition in a liver transplant patient.

A man's skin condition and poor diet led to a scurvy diagnosis.

Skin problems are common after stem cell transplants, and early treatment by dermatologists can improve patient outcomes.

Women with PCOS have more severe liver disease.