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Hair removal with intense pulsed light can cause rare skin lesions that are hard to fully treat.

The girl's skin condition is benign but challenging to treat due to its size and location.

A 50-year-old woman with breast cancer developed an autoimmune skin disorder, highlighting the need for thorough checks and team-based treatment.

Lichen planus is linked to several autoimmune diseases.

Tjalma Syndrome is a rare condition in people with lupus, causing fluid buildup and high CA-125 levels, but not due to tumors.

Early treatment of fibrosing alopecia in a pattern distribution may improve outcomes.

Immunomodulatory therapies are effective for treating cutaneous lymphoma, particularly in early stages.

Platelet-rich plasma may successfully treat lichen planopillaris, as shown by one patient's symptom regression.

EPDS and MS might share an immune-related cause.

A woman with X-linked chronic granulomatous disease developed lupus-like skin lesions, improved with treatment, suggesting a unique skin condition in carriers.

A young man with an unusual type of scarring hair loss suggests a possible new variant of a known scalp condition.

Red dots on the upper chest may be an early sign of certain types of hair loss.

Pemphigus vulgaris involves specific immune cells and B cells that produce antibodies causing skin blisters.

Skin problems are common in lupus, important for diagnosis, and can be triggered by sunlight.

The document concludes that a woman has both Frontal Fibrosing Alopecia and Lichen Simplex Chronicus, a previously unreported combination of conditions.

New insights show Lichen Planopilaris is a rare, scarring hair loss condition, hard to treat, mainly affecting middle-aged women, and significantly impacts mental health.

A 29-year-old man had a jaw plaque diagnosed as follicular mucinosis, linked to nestin-positive hair follicle stem cells.

Researchers found a potential new type of skin growth called follicular mucinous nevus.

Metabolic issues may trigger lymphocytic cicatricial alopecia, and treatments targeting these issues could help.

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.

Scalp disease in dermatomyositis causes significant symptoms and has unique features.

A young woman had a rare, usually non-cancerous tumor on her face that was initially mistaken for a different condition.

A 66-year-old woman's thick scalp and hair loss were confirmed as lipedematous alopecia, a rare condition possibly influenced by genetics, with no effective treatment known.

Bullous pemphigoid, intrahepatic cholangiocarcinoma, and alopecia areata may share immune-related causes.

Generalized trichoepitheliomas with hair loss may indicate myasthenia gravis.

Early recognition and treatment of LPP can prevent hair loss and improve quality of life.

A woman with a rare scalp condition causing a thick scalp and hair loss didn't improve with steroid treatment.

Upper eyelid hyperpigmentation can help diagnose facial lichen planus pigmentosus in patients with frontal fibrosing alopecia.

The lump on a woman's scalp was a rare, potentially cancerous tumor from the hair follicle, not a common cyst.

TB lymphadenitis can occur in people with weakened immune systems, like those with SLE.