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Two patients with the same genetic mutation had both blistering skin and easily pulled out hair.

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

Pigmented papules on the ear can be a rare skin condition called cutaneous amyloidosis, treatable with topical tretinoin.

The study found that polymorphous light eruption varies among patients and can be distinguished from benign summer light eruption by the time it takes for symptoms to appear after sun exposure.

The treatment significantly improved lymphocytic cicatricial alopecia symptoms in most patients.

A rare scalp tumor was removed from a 49-year-old woman, with a good outlook if benign but needing careful monitoring if malignant.

Discoid lupus erythematosus involves immune activation and fibrosis around hair follicles, with shared pathways across humans, dogs, and mice, suggesting potential treatments for both humans and animals.

Hair loss is common in lupus patients and can be permanent or reversible, depending on the type, with various treatments available.

Cicatricial alopecia can progress to complete hair loss, making diagnosis and management difficult.

Fox Fordyce disease might be more common in prepubertal girls than thought and can be managed with treatment.

Black hairy tongue can be an early sign of graft-versus-host disease after stem cell transplants.

Combining baricitinib with UV-B therapy effectively treats non-segmental vitiligo and is well-tolerated.

Lupus erythematosus can mimic alopecia areata, and trichoscopy is key for accurate diagnosis and better patient outcomes.

A 16-year-old boy with Castleman's disease and lupus was successfully treated and showed no recurrence.

Systemic lupus erythematosus treatment can restore vision in patients with retinal artery occlusion.

Lenalidomide effectively and safely treats skin symptoms in pediatric lupus, reducing the need for prednisone.

A baby had a rare condition with abnormal blood vessels in the brain and unusual skin and hair growth, possibly a new syndrome.

Patients with systemic lupus erythematosus and hair loss had fewer hair follicles and non-scarring alopecia; direct immunofluorescence was not helpful in diagnosing lupus in these cases.

Telitacicept effectively improved hair regrowth in a woman with lupus and alopecia.

Two sisters with lipoedematous scalp suggest a genetic influence in the condition.

A 70-year-old woman with bronchiectasis developed a rare immune disease due to a bacterial infection, requiring a difficult balance of treatments.

Two boys developed a viral skin infection during chemotherapy, which resolved with improved immune function.

Current SLE classifications need refinement, and the complement system is a key therapeutic target.

An 18-year-old girl with pemphigus vulgaris needed strong medication and careful treatment due to ineffective initial therapies and side effects.

Pimozide treatment resolved cysts and partially restored cheek fat in a man with Barraquer–Simons syndrome.

The document suggests that severe hair loss in SLE patients may be an early sign of scalp DLE, treatable with immunosuppressive therapy.

A girl with Becker naevus syndrome has a genetic variant in the ACTB gene related to her symptoms.

Two patients had a rare combination of red skin spots and white scaly skin lesions not on the genitals.

Pseudopelade is likely an independent disease due to its distinct features.

Lichen planopilaris can be triggered by prolonged scalp traction and can be treated with corticosteroids.