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A 66-year-old woman's thick scalp and hair loss were confirmed as lipedematous alopecia, a rare condition possibly influenced by genetics, with no effective treatment known.

A rare skin condition in a baby showed unusual fat and hair follicle changes.

Early diagnosis and treatment are crucial for managing Berardinelli–Seip syndrome.

Nevus psiloliparus lacks mature hair follicles but keeps other skin structures intact.

A woman with lupus and systemic sclerosis developed severe acne that didn't improve with treatment and died from pneumonia and septic shock.

A 59-year-old woman was diagnosed with a rare hair loss condition called lipedematous alopecia.

A man with severe leprosy developed painless ulcers and numbness, treated successfully with multiple drugs and vitamins.

Injection lipolysis effectively reduces small fat deposits and should be done with care and proper patient selection.

A woman with a rare scalp condition causing a thick scalp and hair loss didn't improve with steroid treatment.

Lipedematous scalp is mainly caused by an increase in fat tissue under the skin and is different from lipedematous alopecia.

A rare skin condition causing scarring was successfully treated with topical erythromycin and benzoyl peroxide.

Lipedematous alopecia involves a thickened scalp and hair loss, with limited effective treatments available.

Lipedematous scalp may have a genetic link and could be associated with psychiatric conditions.

Lipedema is a painful fat disorder in women that's hard to treat, often worsens with hormonal changes, and requires symptom-focused therapies.

Troglitazone increases subcutaneous fat in lipodystrophy patients.

Three white adults had a rare scalp condition with increased fat and sometimes hair loss, suggesting it's not limited to black women and might be more widespread.

A patient with a thick scalp and hair loss was correctly diagnosed with alopecia areata and a thick scalp fat layer, not lipedematous alopecia, and regrew hair after treatment.

Lower lipin 1β in belly fat is linked to insulin resistance in people with polycystic ovary syndrome.

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

Lipedematous scalp may be underdiagnosed and doesn't improve with finasteride.

Taiwan reported its first case of a rare scalp condition with no clear cause or treatment.

An elderly woman's upper lip lump, thought to be a mucocele, was actually a rare type of lymphoma usually found on legs, treated successfully with chemotherapy and radiation.

A cat with a rare pancreatic tumor and diabetes died despite treatment, showing similar symptoms to a human condition.

Improved nutrition quickly healed the patient's skin lesions.

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

The woman was diagnosed with lichen sclerosus, a rare skin condition, after initial misdiagnosis and ineffective treatments.

A 5-year-old girl with a rare genetic disorder, lipoid proteinosis, showed reduced new lesions but persistent scars after avoiding skin trauma.

COVID-19 may lead to severe skin necrosis without clear underlying causes, as seen in a diabetic patient who required leg amputation.

Two sisters with lipoedematous scalp suggest a genetic influence in the condition.

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