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A boy's hair loss improved after tumor removal and vitamin D treatment, but hair loss returned despite normal vitamin D and no tumor regrowth.

Removing both ovaries treated the woman's excess male hormone symptoms.

A man's health improved after treating his undiagnosed adrenal insufficiency, which caused fatigue and weight loss.

A thorough diagnostic process and teamwork are crucial for managing complex hyperandrogenism in postmenopausal women.

Most dogs with adrenal-dependent hypercortisolism had normal blood pressure after one year of treatment or surgery.

Removing an adrenal tumor can significantly reduce high androgen levels in postmenopausal women.

A rare case of Cushing syndrome was successfully treated with one-sided adrenal gland removal, suggesting personalized treatment is important.

A 13-year-old girl's masculine symptoms improved after surgery for a rare adrenal tumor that produced male hormones.

A boy with a new NR5A1 gene mutation has a sex development disorder without affecting his adrenal glands.

Long-term treatment with buprenorphine/naloxone for opioid addiction may lead to secondary adrenal insufficiency.

A patient produced cortisol after adrenalectomy, possibly due to residual tissue or other body parts making steroids.

The case shows the importance of quick and thorough evaluation of adrenal tumors to prevent rapid disease progression and poor outcomes.

Long-term opioid use can cause a serious condition where the adrenal glands don't work properly, which doctors should watch out for.

A rare adrenal tumor in a woman only made DHEA-S, causing hair thinning, and was removed, fixing the hormone level.

The document concludes that patient outcomes for Congenital Adrenal Hyperplasia are often not ideal because of poor management and a need for better diagnosis and treatment methods.

Using GnRHa agonists helps diagnose and treat ovarian hyperthecosis when surgery isn't possible.

A woman's adrenal tumor disappeared after treatment with cyproterone acetate.

A woman's Cushing's syndrome caused by adrenal cancer improved after surgery.

The document concludes that proper diagnosis and a multidisciplinary approach are crucial for managing Congenital Adrenal Hyperplasia effectively.

The document concludes that Nonclassic Congenital Adrenal Hyperplasia requires personalized treatment plans to manage symptoms and fertility, with glucocorticoids being a common therapy.

Intralesional steroid injections can effectively treat calcinosis and ulcers in scleroderma.

High androgen levels and genetic factors likely cause Becker's nevus and related symptoms.

Nonclassic congenital adrenal hyperplasia is a genetic disorder causing hormone imbalances, affecting fertility and requiring personalized treatment.

Rare adrenal cancers that secrete androgens or estrogens have a poor prognosis and are treated primarily with surgery.

Children with classic congenital adrenal hyperplasia have thicker heart fat and are at higher risk for heart problems and early atherosclerosis.

A genetic marker linked to a type of hair loss was found in most patients studied.

Ectopic adrenal rests can cause androgen excess after adrenalectomy and may need targeted surgery.

Women with congenital adrenal hyperplasia showed no prostatic growth.

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

Hair steroid measurement is an effective method to diagnose and monitor CAH in developing countries.