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Neoadjuvant endocrine therapy led to a better future outlook than chemotherapy, with no major quality of life differences.

A man's rare adrenal tumor caused feminization and white hair, was removed surgically, and improved after treatment.

Ovarian steroid cell tumors can mimic adrenal hyperplasia, and surgery can normalize hormone levels.

An 8-year-old boy's early puberty was caused by a rare hormone-secreting brain tumor, which was successfully treated with surgery.

A rare ovarian tumor in a 2-year-old girl was successfully removed, normalizing her hormone levels.

Surgical removal of an adrenal tumor resolved hormonal issues in a young woman.

A woman with anorexia and Cushing's syndrome improved after tumor removal, highlighting the need to consider hormonal issues in psychiatric conditions.

A rare ovarian tumor caused high testosterone and excess hair in a woman, which was resolved after tumor removal.

Early detection of ovarian steroid cell tumors is crucial to prevent lasting symptoms.

A woman's pelvic pain and bleeding led to finding and successfully treating a rare benign tumor in her reproductive system.

A rare ovarian tumor caused high male hormone levels, but surgery fixed it.

Sporadic trichoblastic neoplasms generally don't recur or spread, with one case showing a specific genetic fusion.

Surgery removed ovarian tumors, normalizing testosterone and improving symptoms.

A man's adrenal insufficiency was caused by a pituitary tumor linked to kidney cancer.

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

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

A 70-year-old woman with a malignant adrenal tumor improved after surgery and radiotherapy.

Adrenocortical carcinoma is a rare, aggressive adrenal gland cancer with a poor outlook.

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

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

Pre-surgical embolization and a two-stage resection improve outcomes for rare sacral tumors.

A woman's severe hormone imbalance after menopause led to finding a rare ovarian tumor, treated by surgery.

VHL disease can cause early paragangliomas, needing lifelong monitoring.

Rathke’s cleft cysts can rarely cause Cushing disease, and surgery can improve symptoms.

Trichogerminoma is a rare, benign skin tumor from hair cells, with a small risk of becoming cancerous.

Adrenal tumors should be considered in Addison's disease if unusual results appear, with surgery as a solution.

Rapid virilization should be checked for possible ovarian or adrenal cancer.

MESTSV is a rare tumor that is mostly benign but needs long-term monitoring due to potential recurrence.

A woman's severe male hormone excess was caused by a small, hard-to-find ovarian tumor.

Low leptin levels in obese women with high testosterone may indicate a tumor that secretes male hormones.