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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.

A woman's small, unnoticed adrenal mass turned out to be a rare non-Hodgkin's lymphoma, treated successfully with surgery and therapy.

Congenital adrenal hyperplasia may be linked to adrenal myelolipoma.

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

Frontal fibrosing alopecia in Bogotá mainly affects postmenopausal women, with possible links to hormonal changes and sunscreen use.

Thorough evaluation and treatment are crucial for thyroid nodules.

CYLD deficiency in skin tumors disrupts hair follicle cell processes and protein secretion.

A rare benign tumor was found in a man's scrotum, highlighting the need for accurate diagnosis.

Coinheritance of BRCA2 and CYLD genes may lead to new treatment options for certain cancers.

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

Steroid cell tumors in ovaries are rare, can cause hormone changes, and may be cancerous.

The thyroid nodule was benign, and surgery was successful with a smooth recovery.

A man with kidney tumors and lung cysts was diagnosed with Birt–Hogg–Dubé syndrome and treated successfully, with genetic testing confirming the diagnosis.

A woman's rare adrenal tumor caused high testosterone and cortisol levels, which normalized after the tumor was removed.

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

Lrig1 could be a marker for advanced sebaceous carcinoma.

The nodule on the woman's back was a benign hair follicle tumor, not cancer, but needed removal.

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

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

A postmenopausal woman's excess male hormone symptoms were caused by a rare adrenal gland tissue in her ovary.

LRIG1 is linked to better survival in Merkel cell carcinoma.

A rare scalp tumor was removed from a 49-year-old woman, with a good outlook if benign but needing careful monitoring if malignant.

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.

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

Early diagnosis and surgery can improve symptoms of ovarian hyperthecosis in postmenopausal women.

This is the first known case of parathyroid cancer in a patient with Birt Hogg Dube Syndrome.

High lactate dehydrogenase activity is not necessary for the growth of squamous cell carcinoma.

Castration helped a dog with a tumor and hair loss by normalizing hormone levels and regrowing hair.

The L457(3.43)R mutation in the human lutropin receptor causes increased activity and hormone insensitivity, leading to precocious puberty.

A rare pancreatic tumor caused a woman's male-like features, treated successfully with surgery and medication.