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A 73-year-old woman with Hypopigmented Mycosis Fungoides, a rare skin lymphoma, experienced disease progression despite treatment, emphasizing the need for ongoing monitoring.

A woman with lupus developed a rare skin condition, which improved with increased medication.

The drug TGU was ineffective against small cell lung cancer and caused significant bone marrow suppression.

A rare skin condition linked to leukemia improved with chemotherapy.

Repeated biopsies are crucial for managing lupus panniculitis when initial treatments fail.

Some people with lichen planus pigmentosus might later develop frontal fibrosing alopecia.

A rare skin condition in children can look like other diseases.

A 4-year-old girl with a rare lupus condition was successfully treated with oral corticosteroids, leading to full recovery and hair regrowth.

Upadacitinib effectively treats pyoderma gangrenosum.

Wedelolactone may help treat lung fibrosis by reducing inflammation and lung damage.

A man with severe leprosy developed painless ulcers and numbness, treated successfully with multiple drugs and vitamins.

A patient with a new PLEC gene mutation showed symptoms of both muscular dystrophy and myasthenia gravis, which improved with steroid treatment.

The patient with lupus and Degos' disease showed significant improvement with treatment.

Chitosan-encapsulated Cordyceps militaris reduces lung cell damage from pollution.

TB lymphadenitis can occur in people with SLE on long-term immunosuppressive therapy.

Graft-versus-host disease is a complication where donor immune cells attack the recipient's body, often affecting the skin, liver, and gastrointestinal tract.

Ulcerative sarcoidosis in body folds is rare and improved with prednisone and hydroxychloroquine.

Follicular mycosis fungoides can look like a B-cell lymphoma, making diagnosis difficult.

Surgery with a carbon-dioxide laser successfully treated a Labrador's tongue condition, but some hair regrew.

Diagnosing and managing Glucocorticoid Resistance Syndrome is complex due to genetic differences and varied symptoms.

Elevated granulysin levels may indicate disease activity in vitiligo and alopecia areata.

A man developed unusual growths after a hair transplant, which were treated successfully with no recurrence after a month.

A rare type of skin cancer with mucosal involvement was partially treated but eventually relapsed.

Chronic graft-versus-host disease in the skin shows strong Th1 immune response and unique barrier issues.

Spontaneous keloids may be linked to nephrogenic systemic fibrosis in dialysis patients.

Early recognition and treatment of severe SLE symptoms can improve outcomes.

A 5-year-old girl has lipoid proteinosis, causing voice issues, hair thinning, skin lesions, and tongue movement problems.

Most children with childhood-onset lupus in Baghdad responded well to treatment, but some developed chronic kidney disease or died.

Post-steroid panniculitis is now rare because doctors taper steroids more carefully.

Tjalma Syndrome is a rare condition in people with lupus, causing fluid buildup and high CA-125 levels, but not due to tumors.