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A rare skin cancer on a man's elbow was successfully treated with surgery, showing no recurrence after one year.

Ovarian hemangioma is a rare, benign tumor that can be treated effectively with surgical removal.

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

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

A 79-year-old man was diagnosed with a rare skin condition called nevus comedonicus on his eyelids.

Early adrenal gland maturation in young children can be normal, but other serious conditions should be ruled out first.

Hair follicle hyperplasia is common in both benign and malignant skin lymphoproliferative disorders, with a proposed new term "pseudolymphomatous adnexitis."

Unexplained excessive hair growth can signal underlying cancer and often indicates a poor prognosis.

Men with Addison disease should be screened for X-linked adrenoleukodystrophy if they have hair loss.

Nonclassic adrenal hyperplasia is a genetic condition that can cause early puberty and fertility problems, treated with specific steroids.

A rare ovarian tumor was diagnosed in a woman from North Brazil, and surgery is the preferred treatment.

Inverted follicular keratosis can look like cancer but is actually a harmless tumor.

A rare ovarian tumor caused early puberty signs in a 1-year-old girl, but surgery reduced hormone levels.

A man with a type of skin lymphoma had unusual yellowish skin growths despite normal blood lipid levels, and treatment reduced some symptoms but not the growths.

The patient with a misplaced pituitary gland and interrupted pituitary stalk is being treated with hormone replacement.

A woman's severe male-like symptoms were caused by a rare, benign tumor in her ovary that produced male hormones.

Women with pituitary adenomas often have reproductive issues, like irregular periods and trouble getting pregnant, but not always breast milk production without pregnancy.

A 13-year-old boy with Cushing syndrome has high cortisol levels from a pituitary gland issue and underdeveloped sexual characteristics.

Skin lesions in Carney Complex are caused by a gene change in some skin cells that leads to increased pigmentation and may lead to tumors.

A new benign nail tumor called onychoblastoma was identified.

Researchers found a new ABCD1 gene mutation linked to a rare brain and nerve disorder with unusual brain changes.

PTHrP is higher in certain dog tumors and may act as a local growth factor.

Epidermal nevi are skin cell clusters linked to various syndromes.

Acromegaly can be hard to diagnose in young women with atypical symptoms, and persistent high phosphate levels should lead to growth hormone testing.

A woman with a rare hormone resistance condition also had missing teeth and hair loss, which might be new symptoms of her genetic disorder.

BAP1 mutations are rare in pediatric melanocytic tumors and may develop later in life.

Surgical removal of a rare ovarian tumor improved symptoms and hormone levels in a postmenopausal woman.

Idiopathic hypoparathyroidism is rare and can be managed with dihydrotachysterol.

A rare calcium deposit condition was found on a man's scalp.

Adrenomedullin 2 stops cell growth and causes cell death in human hair follicles.