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An 8-year-old girl with vitiligo developed extra hair growth on her knee after using tacrolimus ointment.

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

Pseudopelade is a rare inherited hair loss condition with a genetic cause.

Trichilemmal cysts can appear on children's eyelids and may be mistaken for other conditions.

A 70-year-old man with skin cancer on both sides of his forehead was treated with surgery and cryotherapy, highlighting the need for early detection and prevention.

A man with itchy skin lesions and weight loss was diagnosed with a rare skin condition linked to a pancreatic tumor.

Nestin-expressing cells turn into a specific type of skin cell in hair follicles during development and in adults.

The document reports a rare case of ECCL with a new association with optic disc colobomas.

Reduced CD44 expression may cause abnormal hyaluronate buildup in cutaneous myxoma.

The woman has a skin condition involving nodules, scars, and hair loss.

The link between pemphigus and the patient's scarring hair loss is still unclear.

Eye exams are crucial for kids with 13q deletion syndrome, tamoxifen can cause vision loss, Propecia may lead to cataracts, Lipoid Proteinosis causes skin bumps, and OCT is useful for diagnosing macular diseases.

The document concludes that a woman has both Frontal Fibrosing Alopecia and Lichen Simplex Chronicus, a previously unreported combination of conditions.

Topical 6% salicylic acid effectively reduced skin plaques in a patient with wooly hair and palmoplantar keratoderma.

Advanced dermoscopy techniques improve diagnosis and treatment monitoring for Kerion celsi but don't guarantee full hair regrowth.

Ustekinumab treatment may reveal a genetic tendency for steatocystoma multiplex in psoriasis patients.

Generalized trichoepitheliomas with hair loss may indicate myasthenia gravis.

A unique case of skin cancer showed unusual calcification, possibly linked to calcium-binding proteins.

An 8-year-old girl had a rare, benign skin tumor on her forehead.

The infant likely has Hay-Wells syndrome and needs genetic testing and heart screening.

Adult hair follicle cells can create new hair follicles from corneal cells with the right support.

Psoriasis can cause rare vulval scarring.

A 2-year-old girl had a hair disorder not shared by her identical twin.

Higher levels of nidogen1 and type IV collagen are found in basal cell carcinoma compared to normal skin.

Hair follicles and sweat glands show different keratin staining patterns.

Mutations in the hairless gene cause hair loss and skin cysts in rhesus macaques.

Sonidegib often causes hair loss, and LC-OCT helps identify early signs.

A 17-year-old in Saudi Arabia was diagnosed with a rare skin condition causing red-brown facial patches.

Removing keratin plugs and ingrown hairs improved scalp inflammation.