Search

everythinglearnresearchcommunity

for

Search:↓

Certain genetic changes in the LSS gene cause a rare skin and hair condition.

Intralesional chemotherapy with 5-fluorouracil and methotrexate may worsen keratoacanthoma-type skin cancer in transplant patients.

Keratoacanthomas on lips may originate differently than those on skin.

A patient's rare benign tumor in the neck was removed successfully with proper function of the facial nerve maintained.

Reflectance confocal microscopy may help diagnose trichofolliculoma by showing specific skin features.

Cutaneous lymphocytosis in cats is a slowly progressing, relatively benign disease affecting older cats, often causing skin lesions and systemic signs.

Dermoscopy helps diagnose unusual skin lesions like osteonevus of Nanta and can prevent misdiagnosis of serious conditions.

The girl has a genetic hair condition causing thin hair since childhood.

The patient's symptoms improved with treatment but recurred when the steroid dose was reduced, requiring ongoing therapy.

Ovarian Leydig cell tumors are hard to diagnose with just advanced imaging; expert ultrasound and clinical evaluation are essential.

The document concludes that permanent hair loss conditions are complex, require early specific treatments, and "secondary permanent alopecias" might be a more accurate term than "secondary cicatricial alopecia."

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

A woman with a rare form of multiple myeloma had a headache and a skull mass, which led to her diagnosis after tests and a biopsy.

Birt–Hogg–Dubé Syndrome requires genetic testing for accurate diagnosis due to its similarities with tuberous sclerosis.

Keratoacanthoma changes as it grows, showing different hair follicle characteristics at each stage.

Monilethrix is a rare hair disorder causing beaded, fragile hair, often improving on its own over time.

β-catenin is essential for stem cell activation and proliferation in hair follicles.

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

Steroid treatment greatly improved the symptoms of a boy with a rare disorder called Satoyoshi syndrome.

Recognizing eyebrow hair loss linked to a rare skin condition is crucial for proper treatment.

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

Benign ovarian tumors can cause excess male hormones and related conditions in postmenopausal women.

Skin organoids with NCSTN mutation show changes in hair follicle development and higher inflammation, key features of Hidradenitis Suppurativa.

A woman with both Cronkhite-Canada syndrome and myelodysplastic syndrome improved significantly with corticosteroid treatment.

The case suggests a possible link between severe acne and certain bone deformities.

Plica polonica is a rare condition where hair becomes irreversibly tangled, and the treatment is to cut the matted hair.

A woman's excessive hair growth was caused by a rare benign tumor in her adrenal gland, which was successfully removed.

Harlequin ichthyosis involves abnormal skin cell structures and giant mitochondria, affecting skin and hair.