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Oral lichen planus is a chronic disease causing mouth discomfort and sometimes needs immunosuppressive treatment.

Managing frontal fibrosing alopecia and lichen planus pigmentosus is challenging due to resistant hair loss and skin discoloration.

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.

A 37-year-old male with severe skin and internal issues has a rare inherited skin condition called dystrophic epidermolysis bullosa.

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

A rare type of skin cancer with mucosal involvement was partially treated but eventually relapsed.

Hair loss can occur in people with systemic lupus erythematosus.

Blood and urine markers are important for diagnosing lupus in children.

EPF can occur without visible pustules.

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

No single biomarker is reliable enough for diagnosing and assessing SLE.

A patient with Rhupus was diagnosed with Rowell syndrome and treated with various medications.

Patients with SLE experienced non-scarring hair loss with fewer hair follicles, and DIF did not help identify lupus.

PEH in vulvar LS is common and needs careful diagnosis to avoid confusion with cancer.

Skin changes in Pseudoxanthoma elasticum patients can indicate the severity of related health issues.

Most clinicians follow discharge guidelines, many lupus patients don't use sunscreen regularly, dithranol is effective for psoriasis, biopsy methods should be based on lesion type, voriconazole may raise skin cancer risk, a new scale can help diagnose female hair loss early, and most melanomas may develop from existing moles.

A new mutation in the PLEC gene causes a rare condition with skin blistering, muscle weakness, and hair loss.

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

The case shows how hard it is to tell apart Multiple Autoimmune Syndrome from other similar autoimmune conditions, but correct diagnosis is key for treatment to work.

Soft-tissue calcification is rare in systemic lupus erythematosus.

A 62-year-old man with diabetes and kidney disease had itchy skin lesions diagnosed as perforating folliculitis, treated with medication and skin care.

Rhupus is a complex syndrome that combines rheumatoid arthritis and lupus, making diagnosis challenging.

Two rare bald spots on the back of the scalp were found to be lupus, not alopecia areata.

Promising treatments for EBS include anti-inflammatory drugs, antibiotics, creams, mTOR inhibitors, and gene editing, but more trials are needed.

Reducing immunosuppression and using antiviral creams improved the woman's skin condition.

Erythematous papulopustular eruptions in cancer patients using EGFR inhibitors show specific skin changes that vary with severity and treatment type.

A woman with inflammatory bowel disease improved after treatment with ustekinumab for a rare skin condition associated with her disease.