Search

everythinglearnresearchcommunity

for

Search:↓

A rare calcium deposit condition was found on a man's scalp.

Pilomatricomas are often linked to genetic syndromes, especially Apert syndrome, and genetic analysis is crucial for diagnosis.

The flap effectively sealed leaks and served as a barrier, with minor complications, for anterior skull base surgery.

A 15-year-old boy had a rare skin growth on his buttock.

A man with a rare scalp cancer was successfully treated, highlighting the need for early management to prevent spread and complications.

A rare adrenal gland tumor can cause unusual symptoms due to hormone changes.

Taiwan reported its first case of a rare scalp condition with no clear cause or treatment.

A man with a birthmark on his scalp developed hair loss that improved with treatment, but the link between the birthmark and hair loss was unclear.

The man's symptoms improved and the tumor shrank after treatment with cabergoline.

There's an urgent need for better treatments for hair loss caused by radiation therapy.

Temozolomide improves survival in grade III glioma patients without harming quality of life.

Accurate diagnosis of facial skin tumors requires detailed analysis to distinguish between benign and malignant types.

Basaloid follicular hamartoma is a rare, benign skin growth often misdiagnosed.

The man had a fungal infection in his knee, treated with surgery and antifungal medication.

Gomez–Lopez–Hernandez syndrome can cause focal hair loss and developmental delays but some children can still function well and excel in school and sports.

A black pore on a man's cheek was a hair follicle tumor and was removed.

A 10-year-old boy recovered from a scalp infection caused by a fungus after treatment with itraconazole.

Ethanol embolization and debridement successfully treated a scalp AVM, stopped bleeding, and restored hair growth.

A rare case showed hair regrowth after chemotherapy for thymoma, suggesting a link between alopecia areata and thymoma.

An 18-year-old boy had a harmless skin nodule near his nose with hair and oil glands inside.

The document reports the first Brazilian case of a girl with Becker nevus syndrome, characterized by skin changes, breast underdevelopment, and scoliosis.

Misdiagnosing kerion as a bacterial infection can lead to unnecessary surgery and permanent hair loss.

A rare eyelid tumor was successfully diagnosed and removed, highlighting the need for careful examination.

Fahr syndrome causes brain calcification and is managed by treating symptoms and underlying issues.

CARASIL can cause different symptoms even with the same genetic mutation.

Hair loss in this case was caused by a tumor, not typical baldness.

MRI can show unusual brain changes in adrenomyeloneuropathy.

A possible link exists between hair follicle abnormalities, hair loss, and muscle weakness.

Trichoblastomas in aged house musk shrews show unique features and may involve serum amyloid A in inflammation.

Some skin growths with mucin can form hair follicles and resemble skin cancer, but a special stain can help tell them apart.