Search

everythinglearnresearchcommunity

for

Search:↓

A young woman had a rare tumor causing high male hormone levels and symptoms like excessive hair and acne. After removing the tumor, her hormone levels returned to normal. Early diagnosis is important.

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

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

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

A woman's ovarian tumor causing high testosterone was successfully removed, and her symptoms improved.

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

A woman's mature cystic teratoma caused her virilization by producing testosterone.

Leydig cell tumors can cause high testosterone in women and are treated by removing the ovaries.

The patient had paraneoplastic pemphigus without mucosal involvement.

Postmenopausal women with excess male hormones may have ovarian tumors, and surgery usually cures them.

A Rathke's cleft cyst caused hormonal imbalances and symptoms in a 68-year-old woman.

Different sebaceous gland diseases can be treated with medications, hormone therapy, or surgical methods.

A woman's excess male hormone symptoms were caused by a rare benign tumor in her ovary.

A patient with untreated congenital adrenal hyperplasia had large benign tumors in her adrenal glands removed, improving her symptoms.

Precocious puberty can signal familial adenomatous polyposis.

A woman's male-like physical changes were caused by two rare ovarian conditions.

A rare, non-cancerous ovarian tumor was successfully treated with surgery, improving the patient's symptoms.

A young woman with skin issues and weight loss improved after treating her pancreatitis and using skin treatments.

Congenital adrenal hyperplasia may be linked to adrenal myelolipoma.

Syringomas likely start in the upper dermis and form distinct luminal structures.

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

A rare case of Cushing's syndrome and pheochromocytoma requires careful re-evaluation to avoid complications.

Improved nutrition quickly healed the patient's skin lesions.

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

Scar tissue may regenerate sweat glands from remaining glands or stem cells.

A 29-year-old man had a jaw plaque diagnosed as follicular mucinosis, linked to nestin-positive hair follicle stem cells.

Canine circumanal glands develop from hair follicle sheath cells, not sebaceous glands, and lack exocrine ducts.

Dermal IgA deposition without symptoms is rare in Dermatitis herpetiformis risk groups.