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Mesothelioma of the tunica vaginalis testis is rare, often high-grade, and has a median survival of about 24 months.

A rare tumor caused unusual hormone production leading to Cushing syndrome.

Glucocorticoid and mineralocorticoid therapy effectively manage Congenital Adrenal Hyperplasia symptoms but have limitations.

A new gene mutation causes complete androgen insensitivity in a 16-year-old with a female appearance.

Norethisterone (jenapharm) therapy is effective for endometrial cancer.

About 2.2% of women with symptoms of high male hormones have a mild form of congenital adrenal hyperplasia, and measuring a specific hormone level can accurately diagnose it.

Early diagnosis and treatment of congenital adrenal hyperplasia are crucial to manage symptoms and prevent complications.

The girl's increased hair growth and other symptoms were due to a hormone-secreting ovarian tumor, which was successfully treated with surgery.

Women with hair loss had higher levels of certain hormones, suggesting a link to a condition like PCOS.

A transwoman developed a brain tumor after nine years of hormone therapy, suggesting a possible link between the treatment and tumor development.

Consider Sertoli-Leydig cell tumors in Peutz-Jeghers syndrome patients with adnexal masses.

The ferret had a malignant apocrine gland tumor and did not survive surgery.

A boy with a rare form of early puberty caused by a new gene mutation responded well to treatment aimed at reducing testosterone and preserving adult height.

The patient likely has Chrousos syndrome, a rare condition causing insensitivity to glucocorticoids, requiring high-dose dexamethasone treatment.

Hair loss in postmenopausal women due to ovarian hyperthecosis is rare, but removing the ovaries can significantly improve the condition.

TURP specimens should be checked for various tumors, not just common prostate issues.

Untreated Congenital Adrenal Hyperplasia can cause severe hair loss due to high androgen levels.

Hidradenitis suppurativa improves with antiandrogen therapy.

Cyproterone acetate is a safe treatment that causes modest feminization in transgender female adolescents, and works better with added estrogens.

The desmopressin stimulation test helped identify an adrenal cause for a patient's Cushing's syndrome.

Surgery to lower high testosterone in postmenopausal women with certain ovarian tumors doesn't significantly affect their metabolism.

The anterior pituitary controls adrenal cortex size and activity through ACTH.

Hirsutism is excessive male-pattern hair growth mainly caused by ovarian hormones, and severe cases may require costly treatment with side effects.

Total testosterone levels can help diagnose androgen-producing tumors and hyperandrogenism in women.

Confirm testosterone levels with advanced tests to avoid unnecessary procedures.

Testing basal 17-HP levels is a good way to screen for nonclassic adrenal hyperplasia in women with high androgen levels.

Prostate cancer can progress even with low testosterone due to internal hormone production in the tumor.

Certain genetic variants increase the risk of resistance to hormone therapy in prostate cancer patients.

Neutered ferrets often develop hyperadrenocorticism, with symptoms like hair loss and lethargy, and androstenedione is a key indicator for diagnosis.

Androgen deprivation therapy might be better for preventing COVID-19 than treating it.