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Topical patidegib gel effectively treats basal cell carcinoma in Gorlin syndrome patients without causing the side effects seen with oral treatments.

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

Vogt–Koyanagi–Harada disease can cause rare hair growth on normally hairless thumb skin.

A rare hair follicle tumor was found on a woman's vulva.

Overexpressing Merkel cell virus proteins in human hair follicles can create clusters of cells that resemble Merkel cell cancer.

A five-year-old girl has a harmless, unchanging bald patch on her scalp.

A six-year-old boy with excessive hair growth and other symptoms may have a genetic link on chromosome 17q, requiring regular medical follow-ups.

A man had rare skin tumors with bone formation and cholesterol deposits.

A 3-year-old girl with skin mast cell buildup and congenital baldness improved with treatment, suggesting a rare link between these conditions.

A rare family case of multiple benign hair follicle tumors was identified, highlighting the need to distinguish them from similar conditions.

Some skin lymphomas can look like common skin issues and need careful testing to diagnose correctly.

Vogt-Koyanagi-Harada disease affects vision and skin, mainly in people with darker skin, and is treated with steroids and immunosuppressants.

Injecting monocyto-angiotropin into hare skin increases hair growth by forming new blood vessels.

Dermoscopy is useful for diagnosing Atrichia with Papular Lesions in children without needing a biopsy.

A woman's scalp nodule was a common, harmless pilar cyst, treated by surgical removal.

A 34-year-old woman had itchy black bumps on her face due to a condition called trichostasis spinulosa.

Segmented hair color changes can indicate active alopecia areata.

The tumor likely shows dual neural crest differentiation.

A painless cheek lump was misdiagnosed but found to be a rare, benign skin lesion called pilomatrixoma, treatable by surgery.

A 23-year-old Syrian woman has two rare hair disorders, and avoiding hair treatments plus using vitamins and minoxidil may help.

Abnormal Hedgehog signaling in blood cancers may help tumors grow and resist chemotherapy, suggesting potential for targeted treatments.

A rare genetic disorder causes sparse hair and vision loss due to a CDH3 gene mutation.

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

Radiotherapy effectively treated a large scalp tumor in an elderly woman, avoiding surgery.

A young man had a rare case of hair cysts on his elbows, which was hard to diagnose and treat.

A 12-year-old boy's rare skin condition improved with topical treatments and may resolve by puberty.

A deletion in the CDH3 gene causes a rare disorder with short hair and vision loss.

The hair erector muscle is involved in various skin conditions and disorders.

Haematospermia is usually harmless but needs careful checking to ease anxiety and find any serious causes.

Dermoscopy is crucial for diagnosing rare scalp tumors like trichofolliculoma.