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A man got six skin cancers within a year after a cell transplant for leukemia but was cancer-free 32 months later; skin checks are important post-transplant.

Trichilemmal cysts can appear on children's eyelids and may be mistaken for other conditions.

The newborn's skin blisters healed without scarring, leaving some light spots, and stopped forming after four months.

Sox9 levels in brain stem cells affect whether they stay as stem cells or become neurons.

The child was diagnosed with cutaneous leishmaniasis.

Bexxar is highly effective as a first treatment for non-Hodgkin's lymphoma, with most patients alive and many in remission after eight years.

Metreleptin treatment significantly improved metabolic health in a boy with congenital generalized lipodystrophy.

Trichofolliculomas can sometimes be more aggressive than thought.

Check hormone levels and blood counts before surgery in dogs with abnormal blood cell counts.

Early subungual melanoma might be treated with less aggressive surgery because it invades the skin under the nail more slowly.

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

K15 staining helps distinguish basal cell carcinoma from trichoepithelioma.

Stopping mitochondrial respiration can prevent brain cancer spread in skin cancer patients, and plant compound β-sitosterol could help achieve this.

CEP135 may predict cancer outcomes, and targeting PLK1 could help treat certain sarcomas.

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

Larger nail cavity sizes suggest benign tumors, while smaller ones may need further biopsy to rule out cancer.

Mother and son diagnosed with a rare genetic hair loss condition with no effective treatment.

Skin can produce blood cells, often due to disease, which might lead to new treatments for skin and blood conditions.

The Bethesda system is effective for identifying thyroid cancer but has low sensitivity.

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

The STIM1 R304W mutation in mice leads to bone changes and teeth hair growth.

An 11-year-old girl with hair thinning was diagnosed with monilethrix and early androgenetic alopecia.

High MUC-18/MCAM levels in blood indicate a worse outlook for melanoma patients.

A 15-year-old boy was correctly diagnosed with a rare skin condition after initially being misdiagnosed.

A baby girl has a hair disorder called monilethrix, causing fragile hair that may improve over time.

A transwoman developed a brain tumor after nine years of hormone therapy, suggesting a possible link between the treatment and tumor development.

Biological therapy boosts the immune system to effectively fight melanoma.

Woman with diabetes had hair loss due to rare ovarian tumor; surgery improved hair growth.

Scalp melanomas are more dangerous and likely to recur or cause death than other head and neck melanomas.

New findings suggest the protein linked to Birt–Hogg–Dubé syndrome is important in cell signaling and could affect treatment understanding.