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PRAME helps distinguish between benign and malignant skin cells in most cases.

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

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.

Sun exposure after laser hair removal can cause skin darkening, which is hard to treat and requires avoiding UV light.

A woman with a rare scalp condition causing a thick scalp and hair loss didn't improve with steroid treatment.

A rare skin condition in a boy is likely due to a specific genetic mutation pattern.

Lichen planus pigmentosus may indicate undetected hepatitis C infection.

The study found increased skin pigmentation and variable melanocyte density in a patient with Addison's disease.

Retinoids or their analogs could treat skin pigmentation disorders like melasma and vitiligo.

Excessive eyelash growth from erlotinib may indicate positive tumor response and help treat madarosis.

Dermoscopy can help diagnose oral lichen planus by identifying specific patterns.

Surgical repigmentation can permanently restore color to white hair in vitiligo patients.

Early diagnosis and treatment are crucial for managing Folliculotropic Mycosis Fungoides on the scalp.

The PML protein helps prevent skin cancer in mice.

Acitretin effectively prevented skin cancer in a patient with late-onset Rothmund-Thomson syndrome.

Trichoblastoma in the breast can be mistaken for cancer, so expert review is crucial to avoid misdiagnosis.

Dermoscopy greatly improves melanoma diagnosis and reduces unneeded surgeries.

A 10-year-old boy was diagnosed with a rare scalp condition causing hair loss and treated with a topical cream.

Early detection and treatment are crucial to prevent irreversible hair loss in Lichen Planopilaris.

Langerhans' cells are not involved in hair depigmentation in these mice.

The first Japanese case of a genetic hair disorder caused by specific mutations in the LIPH gene was identified.

Linear lichen planopilaris can affect the trunk, not just the face.

A rare skin cancer on a man's elbow was successfully treated with surgery, showing no recurrence after one year.

The document concludes that ERBB2 mutations are common in extramammary Paget disease and may respond to systemic treatments like cancer immunotherapy.

Latanoprost therapy potentially caused a woman's white hair to darken again.

Melanocyte stem cells hold promise for skin regeneration and treating pigmentation issues.

A girl with Becker naevus syndrome has a genetic variant in the ACTB gene related to her symptoms.

A rare skin condition was identified and planned for treatment in an elderly man.

The tumor on the man's nose was a rare type called pedunculated follicular hamartoma.