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An elderly woman's upper lip lump, thought to be a mucocele, was actually a rare type of lymphoma usually found on legs, treated successfully with chemotherapy and radiation.

HAT-MSCs can effectively engulf harmful microbes and particles, aiding infection treatment.

Using healthy donor stem cells can potentially calm overactive immune cells and reduce inflammation in severe hair loss patients, offering a possible treatment method.

Trichoscopy effectively visualizes scalp micropigmentation without invasive methods.

Only skin melanocytes, not other types, can color hair in mice.

Early and accurate diagnosis of congenital smooth muscle hamartomas is crucial to distinguish them from other conditions.

The Fas/FasL pathway may play a role in alopecia areata.

MITF and WNT3A are key in Dun Mongolian horse pigmentation.

A specific type II hair keratin was identified and found in hair cortex and tongue cells.

People with myotonic dystrophy type 1 have a higher chance of getting skin tumors, including melanoma.

Disruptions in hair follicle fibroblast dynamics can cause hair growth problems.

Increasing Wnt5a in mice skin delays hair growth but doesn't stop it.

Encapsulating hair loss drugs in cyclodextrins improves their solubility and reduces scalp irritation.

Fluorescent proteins help visualize and understand tumor blood vessel growth.

Erythema multiforme-like lesions can occur in lupus without drug use or herpes infection.

Excimer laser therapy can be an alternative for treating superficial morphea when topical steroids don't work.

Dexmedetomidine-loaded microneedles effectively reduce pain without sedation.

CMG2 and TEM8 receptors have distinct roles in skin and growth disorders, affecting collagen breakdown and growth.

Sex steroids affect the MafB gene differently in male and female hamsters.

The p.P25L mutation in the KRT5 gene causes a rare skin condition that worsens over time and may lead to hair loss starting in young adulthood.

A 47-year-old man's eyelid swelling didn't improve with basic treatments, so a biopsy was needed.

Monocyte-derived dendritic cells play a key role in UVB-induced skin sensitivity and inflammation.

A new MTX2 gene mutation caused a severe genetic disorder in a young Chinese girl.

A rare genetic mutation caused severe symptoms in a 6-year-old girl with mandibuloacral dysplasia type A.

Scleroderma patients have lower hair miR-29a levels.

The keratin 5 mutation in a family with epidermolysis bullosa simplex was due to mosaicism, not a new mutation.

People with myotonic dystrophy type 1 tend to develop basal cell carcinoma at a younger age but not more frequently than others.

Overexpression of IKZF1 and Ikaros causes hair loss in mice similar to alopecia areata.

Pretibial myxedema can occur with Graves' disease, showing skin changes like waxy plaques and swelling.

A patient with steroid sulfatase deficiency had a unique hair pattern and a brain malformation not previously linked to the condition.