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Hidradenitis suppurativa tunnels have different microenvironments, suggesting targeted treatments could be more effective.

Targeting CD169+ skin macrophages may help treat psoriasis.

Sentinel lymph node mapping is safe and effective for early-stage ovarian cancer but isn't yet standard practice.

Blocking the CXCR3 receptor reduces T cell accumulation in the skin and prevents hair loss in mice.

Recurrent pneumothorax can occur in Sjogren's syndrome, even without common markers.

Lipocartilage is a new type of tissue that affects hair growth and cartilage regeneration.

Mice with human fetal thymic tissue and stem cells developed symptoms similar to chronic graft-versus-host disease.

BKN-1 antibody targets specific keratin in basal cell epithelioma and normal skin basal cells.

A rare genetic mutation causes severe immune issues, hair loss, and nail problems.

Tranilast successfully treated a man's skin sarcoidosis when other treatments failed.

A dog had a rare skin tumor called desmoplastic tricholemmoma.

Certain blood markers, especially MLR, can help diagnose alopecia areata.

CYLD mutations cause a variety of skin tumors with symptoms starting around age 16, and treatments are currently limited.

Certain leukemia drugs can cause severe skin reactions that may require stopping treatment.

Lower levels of MYLK and CALD1 in bladder cancer and osteosarcoma are linked to worse survival rates.

Lupus pneumonitis can mimic tuberculosis and should be considered in diagnoses.

Some skin conditions are associated with other serious diseases, and office microscopy may miss many fungal infections.

Trichogerminoma is a rare, benign skin tumor from hair cells, with a small risk of becoming cancerous.

Cells that move well may improve hair loss treatments by entering hair follicles.

Recent findings in cell biology help understand cell roles in health and disease.

A rare ovarian tumor can occur without causing male-like symptoms.

IFN-γ and IL-2 are important for T cell activation in hair loss in mice.

A five-month-old boy with Omenn syndrome successfully recovered after a stem cell transplant with reduced intensity conditioning.

Unique fat cells near fibrotic areas contribute to systemic sclerosis progression.

A TNFAIP3 gene mutation can cause unusual and varied symptoms of lupus and Sjogren's syndrome.

Doctors used a special blood sampling technique to diagnose a woman's rare ovarian tumor that was producing male hormones.

Ixekizumab may be an effective first treatment for a rare skin condition causing hair loss.

Keratin 79 cells help form and regenerate hair canals.

Polythelia pilosa is a type of extra breast tissue with hair and should be classified as such.