Search

everythinglearnresearchcommunity

for

Search:↓

A rare skin reaction from cancer treatment was successfully managed with topical treatments and antihistamines.

Surgical removal of a scalp keratoacanthoma is effective and prevents recurrence, but hair may not regrow.

Eyebrow reconstruction using hair follicle grafts was successful in a man with a benign hereditary disorder affecting his eyebrows.

A rare genetic disease caused severe, worsening hair loss from early childhood with poor treatment results.

The review found that basal cell carcinomas on the scalp are not more aggressive than those in other locations.

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

The four patients have a unique type of ichthyosis affecting hair follicles.

Early diagnosis and aggressive treatment are key for managing rare scalp disorders that cause permanent hair loss.

Congenital atrichia with papular lesions causes permanent hair loss and skin bumps from birth.

A 90-year-old woman's hand lesion was a rare, aggressive skin cancer treated successfully with surgery.

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

The woman's forehead lesion was caused by ointment use and resolved with treatment.

This rare genetic disorder causes permanent hair loss and skin bumps from birth.

Keratoacanthomas and squamous cell carcinomas have similar keratin patterns, making them hard to tell apart.

An 8-year-old girl has a rare genetic disorder causing complete, irreversible hair loss and skin bumps.

A 19-year-old male had two rare skin conditions causing scarring and permanent hair loss.

Nagashima-type palmoplantar keratosis in Asians is caused by a SERPINB7 gene mutation.

A girl with a rare skin condition improved after one month of treatment with acitretin.

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

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

The man's hair loss and skin papules were diagnosed as atrichia with papular lesions, not alopecia areata universalis.

The study found clear differences in lesion distribution and microscopic features among trichostasis spinulosa, keratosis pilaris, and eruptive vellus hair cysts.

Keratoacanthoma comes from hair follicle cells.

A new type of pachyonychia congenita may exist, caused by a different keratin mutation.

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

Lichen planopilaris is a rare, chronic condition causing hair loss, mainly in middle-aged women, and early treatment is important to prevent permanent baldness.

A new type of pachyonychia congenita linked to a specific keratin gene mutation was found in two Pakistani families.

Clouston syndrome can lead to skin cancer, so monitoring is crucial.

A rare skin condition called linear lichen planopilaris caused itchy red bumps and hair loss on a man's face.