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Retinoids increase steroid sulfatase activity in leukemia cells through RARα/RXR and involves certain pathways like phosphoinositide 3-kinase and ERK-MAP kinase.

Monoclonal antibodies LT-1, LT-2, and LT-7 help diagnose certain blood cancers.

COVID-19 vaccination may trigger recurrence of cutaneous T-cell lymphoma in some patients.

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

A man with a weakened immune system was diagnosed with a rare skin condition called trichodysplasia spinulosa using skin examination techniques.

A new medical syndrome may include skin changes, hair loss, sweating issues, bone malformations, leg swelling, and low cortisol.

Two patients with Cronkhite-Canada syndrome achieved remission after treatment.

Melanocyte stem cells can become melanoma, resembling human melanoma.

A new test helps find drugs to treat head and neck cancer by targeting c-Rel.

Skin aging and cancer development are influenced by the competition between stem cells.

The lemur's testicular tumor was removed, improving its coat and behavior, with no signs of cancer spread.

Elderly patients with CCCA were all African American with low vitamin D, but no iron or zinc deficiencies, and no hormonal imbalances compared to younger patients.

Three genes linked to the development of trichilemmal cysts were found.

SLE patients often face depression and anxiety due to physical changes, with African-American and Hispanic patients having higher unmet psychological needs.

Shrinking skin cancer increases the chance of cancer in nearby lymph nodes.

Beige and leaden pigment genes act within melanocytes, affecting pigment patterns.

A 78-year-old man with Cronkhite-Canada syndrome improved significantly after treatment and remains symptom-free.

Genetic testing is crucial for diagnosing and treating acrodermatitis enteropathica effectively.

A man was diagnosed with a rare form of lupus after showing unique skin symptoms that responded well to treatment.

Gender-specific analysis could improve treatment for childhood systemic lupus erythematosus.

A woman with Budd-Chiari syndrome improved after treatment and needs a liver transplant, highlighting the importance of considering non-criteria antiphospholipid syndrome in similar cases.

RCM and dermoscopy help identify different types of hair loss in children.

ECM1-modified stem cells can effectively treat liver cirrhosis.

Two siblings have a rare genetic condition causing curly, coarse hair.

Cord blood platelet-rich plasma may safely improve vulvar lichen sclerosus symptoms.

Removing PLCg1 from skin cells caused thicker oil glands and less hair in mice.

Biopsy is crucial for accurately diagnosing EPDS to avoid mistaking it for SCC.

Living with lupus as both a patient and doctor improved understanding and care for others.

A woman with a new PTCH gene mutation has both Gorlin syndrome and severe hair loss.