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SLE affects lungs and kidneys similarly due to immune complexes.

Cutaneous lupus patients have higher levels of certain immune cells in their blood and skin.

Most patients with Lichen planopilaris improved with acitretin, but treatments often didn't work well; preventing infection in skin surgery is important, and bupivacaine might be a better anesthetic.

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

Follicular mycosis fungoides can look like a B-cell lymphoma, making diagnosis difficult.

A woman with Lupus Vasculitis improved after treatment with steroids and other medications.

CD4+ lymphocytopenia can occur in patients with systemic lupus erythematosus.

The patient's scalp lesions stabilized with a combination of treatments after initial therapies failed.

Lichen planopilaris can be accurately diagnosed and effectively treated.

A man developed a rare skin condition and drug-induced lupus, highlighting the need for biopsy in diagnosing skin issues caused by sunlight.

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

Timely diagnosis and aggressive treatment with high-dose steroids and B-cell depletion therapies are effective for severe acute cutaneous lupus.

Erosive lichen sclerosus is a distinct subtype with specific skin features, and treatment led to complete resolution in half of the cases.

Foreign-body granuloma may be a marker for late-stage Lichen Planopilaris and should be considered in diagnosis.

Skin problems are common and early signs of Systemic Lupus Erythematosus, and certain immune system markers are important for diagnosis and treatment.

This type of hair loss is probably often missed and treatments reducing inflammation might work well.

A young woman with lupus developed tuberculosis due to weakened immunity from her medication, showing the need for better TB screening in such patients.

Some patients with a type of skin lymphoma can experience a rare, non-scarring hair loss that looks like another hair loss condition but has distinct features.

Lichen planus pigmentosus and fibrosing frontal alopecia in Colombia are likely different stages of the same disease.

Lichen planopilaris can unusually affect only the face, causing pigmentation and scarring.

HTLV-1-associated lichenoid dermatitis (HALD) is linked to an immune response against HTLV-1-infected cells.

Early diagnosis and treatment can lessen the impact of cicatricial alopecia.

Most treatments for lichen planopilaris were found to be generally unsatisfactory.

Graham-Little Piccardi Lassueur Syndrome is a rare skin condition with specific hair loss and skin symptoms.

Early detection and treatment of primary biliary cirrhosis and related autoimmune diseases improve outcomes.

Surgical excision is an effective treatment for persistent nodules from poly-L-lactic acid injections.

A 59-year-old woman was diagnosed with a rare hair loss condition called lipedematous alopecia.

A woman in Sri Lanka was diagnosed with lupus after presenting with protein loss from the gut and other symptoms.

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

A 5-year-old girl has lipoid proteinosis, causing voice issues, hair thinning, skin lesions, and tongue movement problems.