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A large scalp tumor was removed from an elderly woman, who was later diagnosed with schizophrenia.

Using calvarial bone for maxilla augmentation is less painful and allows for single-procedure dental implants.

The case suggests that dissecting cellulitis of the scalp can occur in a White child and should be considered when diagnosing pediatric scarring alopecia.

Three siblings had both Vohwinkel's disease and congenital alopecia, with no effective treatment.

Scalp medical tattooing effectively camouflages bifid parietal whorls.

Using titanium mesh and thigh tissue is effective for complex scalp reconstruction.

The tumor likely shows dual neural crest differentiation.

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

Children with cancer had slightly more unusual facial shapes than healthy kids, but not enough to easily tell them apart.

EPI-NCSCs from hair follicles may help treat brain development issues in mice.

A young girl had a rare neck cyst removed and needs careful monitoring for related health issues.

A young woman had a rare, usually non-cancerous tumor on her face that was initially mistaken for a different condition.

The lump on a woman's scalp was a rare, potentially cancerous tumor from the hair follicle, not a common cyst.

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

The study concluded that scalp tumors show different patterns based on age, gender, and tumor thickness, and emphasized the importance of early detection and scalp examinations.

The report shows that a rare benign tumor was successfully removed from inside the mouth to avoid scarring on the face.

Reconstructing lower face gunshot injuries with a fibula and scalp flap is effective and gives good long-term results.

Genetic hair shaft abnormalities can be seen with microscopes and often affect scalp hair.

Complete removal of scalp tumors is crucial, but malignant cases may recur or metastasize, requiring a multidisciplinary approach and close follow-up.

Technique effectively reconstructs large scalp defects with minimal hair loss and visible scarring.

A 9-month-old baby had a rare, persistent ring-shaped hair loss condition.

Mutations in the TSPEAR gene cause a new form of ectodermal dysplasia affecting hair and tooth development.

Managing rare genetic diseases like osteogenesis imperfecta and Escobar syndrome is complex and requires both medical and surgical treatments.

Combining microsurgery with craniofacial reconstruction improves aesthetic results and reduces harm to the area where tissue is taken from.

The neck mass was a rare benign "wattle," surgically removed for diagnosis and appearance.

A boy had a rare scalp condition with thickened skin and different-colored hair.

Cerament effectively corrected forehead irregularities in one patient, and various surgical techniques successfully reconstructed perioral soft tissue in 14 patients.

A 21-year-old had a rare developmental anomaly with a misplaced sebaceous gland in a hair follicle.

A 2-year-old boy had no hair and unusual organ placement, and it's unclear if it's genetic or coincidental.