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A patient with a scalp condition and benign skin tumor experienced hair loss and did not improve with treatment, choosing not to have surgery despite a small cancer risk.

Segmented hair color changes can indicate active alopecia areata.

An 11-month-old girl has no scalp or body hair, and the cause is being studied.

A benign tumor developed at a girl's BCG vaccination site, not previously linked to the vaccine.

A young boy's uncombable hair is due to a rare genetic condition that usually improves over time.

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

A 5-year-old boy was diagnosed with congenital triangular alopecia, a type of hair loss without skin changes, usually starting between ages 2-5, with no specific treatment.

A benign tumor on the cheek, called trichoadenoma, should be surgically removed for cosmetic reasons.

A 12-year-old boy with a rare genetic condition has progressive hair loss with no effective treatment.

Some skin tumors may start from hair follicle stem cells.

A 17-year-old girl and her brothers have a rare hair condition with long eyelashes, thick eyebrows, and easily pluckable hair.

A new method can better diagnose eruptive vellus hair cysts.

A six-year-old girl with extra hair on her elbows was treated with hair removal methods.

Some infants temporarily grow scrotal hair, which usually disappears on its own without any health issues.

The study found a specific pattern of uneven melanin distribution on balding scalps that could help understand skin diseases caused by light exposure.

A new benign nail tumor called onychoblastoma was identified.

A young man was unexpectedly diagnosed with basal cell carcinoma after a scalp examination and confocal microscopy.

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

Accurate diagnosis of NLS with dilated hair follicles is crucial to distinguish it from other conditions.

A 12-year-old girl was diagnosed with monilethrix, a genetic condition causing fragile, beaded hair that breaks easily, with no effective treatment available.

A family showed a new condition with inherited hair loss and skin changes, possibly due to one genetic disorder.

Surgeons should know about pilomatricoma for accurate diagnosis, even though it's rare.

A 6-year-old girl was diagnosed with a rare hair disorder called monilethrix.

The study found markers indicating that cells responsible for hair color are differentiating in specific areas of the hair follicle.

A hair cyst can become cancerous, showing specific keratins from the hair sheath.

Trichilemmoma, BCC, and SCC tumors have different stem cell marker expressions.

Mother and son diagnosed with a rare genetic hair loss condition with no effective treatment.