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Some skin lymphomas can look like common skin issues and need careful testing to diagnose correctly.

Digital gangrene can be an unusual first sign of late-onset lupus.

The flaky skin mouse mutation is a natural model for studying human psoriasis.

A 69-year-old woman has a fast-growing hand lesion that didn't improve with salicylic acid.

Excess vitamin A changes skin and hair follicle development and affects polysaccharide distribution.

Buschke-Ollendorff syndrome is a rare genetic disorder causing skin and bone changes, with some cases also showing ADHD or developmental delays.

CSC is linked to mineralocorticoid receptor damage, stress, and steroid use, with treatments including drugs and laser therapies to prevent eye damage.

The model helps understand scar contraction and develop new treatments.

Lipedematous alopecia causes permanent hair loss due to increased scalp fat.

Hair loss in autoimmune blistering skin diseases varies and may regrow with disease control.

The conclusion is that skin, mucous, and eye problems after Stevens-Johnson syndrome and Lyell syndrome significantly affect patients' lives, highlighting the need for comprehensive care and eye check-ups.

Lipedema is a painful fat disorder in women that's hard to treat, often worsens with hormonal changes, and requires symptom-focused therapies.

High-dose corticosteroid treatment helped improve symptoms in a patient with Adult Onset Still Disease.

Claudin-1 is crucial for maintaining skin barrier and preventing inflammation.

A rare lupus case on the chin was successfully treated with steroids and immunomodulators after accurate diagnosis using advanced imaging techniques.

The document suggests a possible link between mast cells and scarring alopecia, recommending more research for potential treatments.

A 60-year-old man with Cronkhite-Canada syndrome improved with treatment, but the condition has a high mortality rate and a risk of colorectal cancer.

A 73-year-old woman with Hypopigmented Mycosis Fungoides, a rare skin lymphoma, experienced disease progression despite treatment, emphasizing the need for ongoing monitoring.

Alopecia areata can show unusual red-dotted vessels and dithranol treatment may mask typical patterns.

A 16-year-old boy's facial condition improved with doxycycline, suggesting an immune response to hair follicle damage.

Consider amyloidosis in patients with specific nail changes and check for systemic issues.

The document reports a rare case of ECCL with a new association with optic disc colobomas.

A new syndrome may link skin, growth, mental, and hair issues.

Early diagnosis and treatment of calcinosis cutis in lupus patients is crucial due to its rarity and potential complications.

LC-OCT can help identify lupus-related scarring hair loss by spotting unique features.

A possible link exists between minimal change nephrotic syndrome and complete hair loss.

Fetal wound healing changes with development, affecting inflammation and collagen, which may influence scarring.

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

Hair loss is common in autoimmune diseases and can be an early sign of the condition, often requiring prompt treatment to prevent permanent damage.

Inherited ichthyoses cause widespread skin scaling and thickening due to gene mutations.