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Adipose tissue and eccrine gland displacement are common in certain alopecias but don't help differentiate between them.

Polymenorrhoea should be included in PCOS diagnostic criteria due to similar metabolic issues.

Pilomatricoma is a rare, benign skin tumor that requires surgical removal for best results.

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

A woman with non-classic CAH had unusual heavy periods and high hormone levels, improved with treatment.

These ovarian conditions cause high testosterone levels.

The patient had complex urinary tract issues and ambiguous genitalia, with physical features suggesting a hormonal imbalance.

BMP4-related anomalies can cause a wide range of eye, brain, and hand/foot problems, and new cases show this variability.

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

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.

More than half of the Thai women with PCOS had polycystic ovarian morphology.

The report described a unique case of Cronkhite-Canada syndrome with unusual polyps and an association with multiple myeloma.

ODC1 gene mutations cause a neurodevelopmental disorder with large head size, hair loss, and facial abnormalities.

Consider TFI in facial hypopigmentation diagnoses and confirm with a biopsy.

A rare skin cancer on a man's elbow was successfully treated with surgery, showing no recurrence after one year.

Inhibiting AP-1 changes skin tumor types and affects tumor cell identity.

A woman with a rare adrenal tumor and hormonal disorder had improved testosterone levels after surgery, but her menstrual irregularities continued.

A newborn girl had a rare case of salivary gland tissue on her chest, which was safely removed.

The tumor likely shows dual neural crest differentiation.

The dog's back mass was a keratoacanthoma with inflammation, successfully removed without recurrence.

A man with a rare adrenal cancer showed unusual symptoms and died four months after diagnosis.

Cantú syndrome may be linked to pituitary adenomas.

Trichoblastic fibroma and basal cell carcinoma are similar but different from trichoepithelioma.

High levels of ODC and a mutant Ha-ras gene cause tumors in mice.

Fine needle aspiration with rapid on-site evaluation is useful for diagnosing pilomatrixoma.

Poromas are related to sweat duct cells, and CK patterns help distinguish apocrine poromas from other neoplasms.

Recognizing diverse presentations of folliculotropic mycosis fungoides is crucial to avoid diagnostic errors.

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

Hair grew in a man's mouth due to a rare condition called heterotopia.