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A PET-CT scan successfully located a hard-to-find Leydig cell tumor in a woman with hormonal symptoms.

A teenage girl with high androgen levels and PCOS developed a rare liver tumor, suggesting a possible link between high androgens and the tumor's growth.

Male accessory sex glands in rats rarely develop tumors and respond to hormones.

A 36-year-old woman with low potassium levels was found to have Cushing disease, and after treatment, her potassium levels normalized.

Insulinomas and adrenocortical tumors are common in older ferrets, diagnosed with blood tests and ultrasounds, and treated with medications or surgery.

Early detection of Cushing's syndrome during pregnancy is crucial to prevent severe complications.

MRI helps distinguish between pituitary adenomas and craniopharyngiomas, guides treatment for pediatric CNS tumors, and assesses rhinocerebral mucormycosis with a high mortality rate in transplanted patients.

Increased ODC activity leads to skin tumors by recruiting stem cells, not by toxic byproducts.

The terrier dog with pituitary-dependent hyperadrenocorticism was successfully treated with mitotane.

Giant pituitary macroadenomas causing Cushing disease are rare and may need extra treatment if surgery fails.

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

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

Skin tumor cells in patients with tuberous sclerosis have higher levels of a protein called cathepsin B.

Most skin adnexal tumors are benign and require histopathological examination for accurate diagnosis.

A young woman had a rare, aggressive ovarian tumor that was hard to diagnose and treat, leading to disease progression despite treatment.

Adrenal tumors in hamsters are rare and hard to diagnose, highlighting the need for better diagnostic tools.

The woman's rare combination of diseases suggests an unknown factor may predispose individuals to multiple endocrine diseases.

High proliferative activity and peripheral invasion indicate malignancy in canine sebaceous gland tumors; the term 'epithelioma' should be updated for clarity.

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

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

The removal of the adrenal tumor improved the patient's symptoms and reduced androgen levels, indicating successful surgery.

Early and accurate diagnosis of congenital smooth muscle hamartomas is crucial to distinguish them from other conditions.

A golden lion tamarin had Cushing's disease due to a pituitary tumor, leading to its euthanasia.

Rare ovarian tumors can cause hyperandrogenism, even if imaging appears normal.

Apocrine type cutaneous mixed tumors often resemble hair follicles, sebaceous glands, and apocrine glands.

A rare ovarian tumor caused high testosterone in a postmenopausal woman, resolved by surgery.

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

Activating β-catenin and inactivating PTEN cause follicular tumors, not papillomas, similar to those in Cowden’s Disease.

The woman's symptoms and tests suggest her adrenal glands are producing too many male hormones.

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