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Somatic BHD mutations are rare in Japanese renal tumors.

A neck lesion misdiagnosed as benign was later treated successfully with Mohs Micrographic Surgery.

Trichoblastic carcinoma may be a distinct type of skin cancer different from basal cell carcinoma.

A man's rare adrenal tumor caused feminization and white hair, was removed surgically, and improved after treatment.

Adrenocortical carcinoma is a rare, aggressive adrenal gland cancer with a poor outlook.

Skin lesions in Carney complex are likely caused by a specific group of skin cells that promote pigment production due to a genetic mutation.

The malignant pilomatricoma showed strong epithelial keratin expression, suggesting it may not calcify.

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

The case shows the importance of quick and thorough evaluation of adrenal tumors to prevent rapid disease progression and poor outcomes.

Trichilemmal carcinoma is rare, usually benign after removal, but needs close follow-up due to recurrence risks.

A man's neck lump was a trichilemmal cyst, not cancer, and should be fully removed due to rare risk of becoming malignant.

The nodule on the woman's back was a benign hair follicle tumor, not cancer, but needed removal.

A rare skin condition in a boy is likely due to a specific genetic mutation pattern.

Folliculotropic mycosis fungoides has unique molecular features and cell interactions that could guide targeted therapy.

Personalized treatment based on detailed tumor analysis successfully managed and reduced the patient's aggressive hair follicle cancer.

A mutation in the KRT86 gene causes hair fragility in a Turkish family.

A new gene mutation linked to Olmsted syndrome may increase cancer risk, suggesting the need for ongoing patient monitoring.

Thyroid tuberculosis can cause hypothyroidism and should be considered when diagnosing cervical masses.

Thorough evaluations and conservative management can lead to positive outcomes in pediatric adrenocortical carcinoma.

The nodule was a benign cutaneous lymphadenoma, not cancer, and was successfully removed.

Dabrafenib was effective and well tolerated in treating thyroid cancer with a specific mutation.

Natural compounds may help treat advanced papillary thyroid cancer by targeting specific molecular pathways.

A woman with a new PTCH gene mutation has both Gorlin syndrome and severe hair loss.

People with Birt-Hogg-Dubé syndrome often have lung problems and delayed diagnosis, and better recognition of CT scan signs could improve diagnosis and management.

New therapies for Birt–Hogg–Dubé syndrome are being developed based on understanding the FLCN gene's role.

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

Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

Two siblings had a rare immune disorder caused by a FOXN1 gene mutation.

Matrical tumors share a common growth mechanism involving the Wnt pathway and consistent PHLDA1 expression.

Generalized trichoepitheliomas with hair loss may indicate myasthenia gravis.