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A young woman's symptoms suggested PCOS, but tests and surgery confirmed and treated a rare ovarian tumor, resolving her condition.

A child with eruptive vellus hair cysts showed some improvement with calcipotriene cream.

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

Unilateral keratosis follicularis squamosa may be a new subtype, successfully treated with asiaticoside ointment.

Hair follicle bumps with stem cells might contribute to permanent hair loss by getting disconnected due to scarring.

Modified β-catenin causes different effects in hair and skin cells, leading to cysts or tumors.

A teenage girl had both a rare ovarian tumor and a severe form of polycystic ovarian syndrome.

A rare skin disorder, nevus comedonicus, can appear on one side of the body following Blaschko's lines.

A person had two different benign skin tumors, a trichoadenoma and melanocytic naevi, at the same time but in different places on the face.

Nevus comedonicus can sometimes grow terminal hair, challenging previous beliefs.

Cathepsin L is essential for normal hair growth and development.

Trichofolliculoma is a unique benign tumor mainly affecting middle-aged adults' faces, often misdiagnosed without histopathology.

ECCL should be considered in patients with specific skin and eye lesions.

Early biopsy is crucial for diagnosing rare skin sarcoidosis, improving treatment.

A man's scalp condition was misidentified as hair loss dots but was actually a common follicular disorder.

Giant keratoacanthoma can look like squamous cell carcinoma, requiring careful diagnosis and surgical removal.

Hair shaft changes may be linked to CCCA, but their role is unclear.

Cylindromas likely originate from hair follicle stem cells, not sweat glands.

The patient with EEC syndrome had scarring alopecia due to deep folliculitis, possibly linked to abnormal hair structure.

Ivermectin and pyrantel pamoate effectively treated the cat's conditions, and restricting activity prevents reinfection.

Dermoscopy is crucial for diagnosing rare scalp tumors like trichofolliculoma.

The skin condition Ulerythema ophryogenes did not improve with treatment in a patient with other birth defects.

Steroid treatment greatly improved the symptoms of a boy with a rare disorder called Satoyoshi syndrome.

Inflammation may cause nail issues in Cronkhite–Canada Syndrome.

Reflectance confocal microscopy can noninvasively diagnose onychomatricoma by showing unique features different from healthy nails or nail fungus.

Mutations in the ACTB gene cause Becker’s nevi and may lead to muscle issues in Becker’s nevus syndrome.

Early diagnosis of tufted hair is crucial for managing folliculitis decalvans, a chronic scalp condition.

Multiple perifollicular fibromas may actually be unrecognized cases of Birt-Hogg-Dubé syndrome.

Netherton syndrome causes specific skin and hair changes that help in early diagnosis.

A 3-year-old girl with skin mast cell buildup and congenital baldness improved with treatment, suggesting a rare link between these conditions.