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Psychological interventions can improve mental health and quality of life in people with alopecia.

The number of new cases of cutaneous B-cell lymphoma has leveled off since the early 2000s, and survival rates have improved since 1973.

An elderly woman's upper lip lump, thought to be a mucocele, was actually a rare type of lymphoma usually found on legs, treated successfully with chemotherapy and radiation.

A new mutation in the FLCN gene linked to Birt-Hogg-Dube syndrome was found, suggesting people with certain lung collapse should be tested for this mutation and screened for kidney and colon cancer.

Dr. Connelly agrees that linear basal cell carcinomas might be more aggressive but highlights the study's lack of clear criteria to identify them.

Clq deficiency is linked to systemic lupus erythematosus symptoms.

NBCCS and BFHS might be the same syndrome, helping better identify and manage cases.

The CLASI is a reliable tool for measuring the severity of cutaneous lupus erythematosus.

Radiological findings help distinguish LAM, PLCH, and BHD to avoid invasive tests.

A woman with chronic hepatitis C had a rare skin condition linked to her illness.

Clouston syndrome is inherited in an autosomal dominant pattern and caused by a specific gene mutation, with no current treatment available.

Clim proteins are essential for maintaining healthy corneas and hair follicles.

CTCL patients can safely continue treatment during COVID-19 with proper safety measures.

The TCL1 transgenic mouse model is useful for understanding human B-cell leukemia and testing new treatments.

CCCA and LPP may be related hair loss conditions influenced by genetics and environment, needing early treatment.

PCFCL may have unrecognized subtypes and needs more research.

Coinheritance of BRCA2 and CYLD genes may lead to new treatment options for certain cancers.

Excluding alopecia and mucous membrane components from the CLASI-A score reduces its effectiveness in capturing important disease activity.

CCCA and lichen planopilaris have similar histological features, making them hard to distinguish.

A new method accurately measures clobetasol propionate in hair and skin.

Thymic LCH may be underdiagnosed, so thymic ultrasound should be considered in infants with cutaneous LCH.

Low-dose chemotherapy is safer, more effective, and cost-effective than surgery for treating bone lesions in children.

Birt–Hogg–Dubé syndrome is a rare genetic condition causing skin lesions, lung cysts, and a higher chance of kidney cancer.

A patient with Birt-Hogg-Dubé Syndrome also had choroidal melanoma, suggesting the need for careful eyelid exams in such patients.

ICL is a condition with low CD4+ T cells like AIDS but not caused by HIV, and normal CD4+ T cell counts may vary between men and women.

Chronic bacterial infections of hair follicles can cause ongoing skin inflammation.

Small bowel lesions in Cronkhite-Canada syndrome persist despite steroid treatment.

A man with kidney tumors and lung cysts was diagnosed with Birt–Hogg–Dubé syndrome and treated successfully, with genetic testing confirming the diagnosis.

Clouston syndrome can lead to skin cancer, so monitoring is crucial.

Black women with CCCA are more likely to have uterine fibroids.