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Different growth patterns in thyroid tumors are influenced by where cell growth and death occur.

Three genes linked to the development of trichilemmal cysts were found.

Non-classic congenital adrenal hyperplasia (NCCAH) can mimic PCOS and requires genetic testing for proper diagnosis and treatment.

Ketoconazole improved symptoms of ACTH-independent Cushing syndrome despite inconclusive initial scans.

Eruptive vellus hair cysts are rare, benign skin lesions that are hard to treat.

A woman had a cyst in her salivary gland, likely from Botox, which was removed and confirmed as an epidermoid cyst.

A woman's excessive hair growth was caused by a rare benign tumor in her adrenal gland, which was successfully removed.

Albumin and prednisone improved symptoms in a woman with Cronkhite-Canada syndrome, revealing potential genetic causes.

A rare case of hair loss was linked to breast cancer spreading to the scalp, but treatment was effective.

CCCA is a common hair loss condition in African American women, often inherited and influenced by hairstyling, with unique scalp features detectable by special tools.

A young man's cheek papule was identified as a benign hair follicle tumor using a skin surface microscope.

CK 15, follistatin, and Bmi-1 can help differentiate basal cell carcinoma from squamous cell carcinoma.

Researchers found a potential new type of skin growth called follicular mucinous nevus.

The 6-year-old Somalian girl fully recovered from her symptoms after successful surgery and treatment.

Some cats with sudden hair loss and tiredness might have cancer-related alopecia.

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

A rare case of severe scalp hair loss and nail issues in keratosis follicularis was observed.

An 8-year-old girl had a rare, benign skin tumor on her forehead.

Keratoacanthoma is a common, usually non-dangerous skin tumor that looks like squamous cell carcinoma but rarely becomes severe.

Scalp biopsies are crucial for diagnosing hair loss causes in cutaneous lymphoma patients.

A rare skin condition with cysts was found on a 5-year-old boy's scalp.

A toddler with a rare adrenal gland tumor causing male-like physical changes was successfully treated with surgery.

Ossification in trichilemmal cysts is more common than previously believed.

Systemic mastocytosis may cause a type of hair loss called cicatricial alopecia.

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

The document discusses various eye conditions and their treatments, including a rare eye cancer in a baby, vision loss from a cancer drug, cataracts from a baldness treatment, a rare skin disorder, and a specific type of eye disease diagnosed with a special imaging technique.

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

Horizontal sections of scalp biopsies are good for diagnosing Central Centrifugal Cicatricial Alopecia and help customize treatment.

A rare skin condition in a baby showed unusual fat and hair follicle changes.