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Triptolide effectively and safely reduces actinic keratosis lesions in mice.

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

Congenital atrichia with papular lesions causes permanent hair loss in children.

A person with thyroid problems had rare, swollen, bald spots on their scalp caused by a condition usually found on the shins.

The condition is likely inherited in an autosomal-dominant pattern.

Phospholipase A2 enzymes play key roles in skin health and disease.

A 29-year-old man had a jaw plaque diagnosed as follicular mucinosis, linked to nestin-positive hair follicle stem cells.

An 8-year-old girl developed a rare skin condition in a linear pattern on one side of her body after a lung infection, which improved with treatment.

Alopecia areata affects hair follicle structure, even in non-balding areas.

sPLA2-IIE is crucial for normal hair follicle structure and skin health.

Plucked hair can help diagnose pemphigus vulgaris early.

An elderly man's non-healing scalp lesion was successfully treated with a strong topical steroid.

The study found that tight junctions reach the top layer of the skin's stratum granulosum, not just the second top layer as previously thought.

A 5-year-old girl with a rare skin disorder was effectively treated with skin creams instead of oral medication.

Triamcinolone acetonide therapy for hair loss may cause a skin condition called linear lichen planus.

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

High proliferation and cell delamination drive early skin development, while later stages may not rely on cell division orientation.

A man with a weakened immune system was diagnosed with a rare skin condition called trichodysplasia spinulosa using skin examination techniques.

The cat's skin condition was resistant to treatment and did not improve.

Epidermal cysts come from the skin, while pilar cysts come from hair follicles.

Combining skin tissue pathology with genetics has greatly improved the diagnosis and understanding of certain skin diseases.

The p.P25L mutation in the KRT5 gene causes a rare skin condition that worsens over time and may lead to hair loss starting in young adulthood.

Congenital atrichia with papular lesions is often misdiagnosed, and new diagnostic criteria can improve accuracy.

Blocking certain proteins in mouse skin can reduce and shrink skin tumors.

Narrowband-UVB phototherapy successfully treated a rare case of Graham Little-Piccardi-Lassueur syndrome.

A rare benign skin growth called melanocytic matricoma was identified in a 69-year-old man.

The patient has a rare skin condition that shows features of two known disorders.

A 4-year-old girl was diagnosed with erythrokeratodermia variabilis after other treatments failed.

A rare scalp infection in a child developed into a kerion with additional skin symptoms.