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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.

Poromas are related to sweat duct cells, and CK patterns help distinguish apocrine poromas from other neoplasms.

A benign skin tumor was removed from a man's leg, and it didn't come back after 9 months.

Rothmund-Thomson syndrome causes skin changes, hair loss, and slightly high lysine and cystine in urine.

A rare nail bed cancer was successfully treated with no recurrence after 4 years.

Adenolipomas may develop from gland entrapment by fat tissue, showing complex and varied forms.

The newborn's skin blisters healed without scarring, leaving some light spots, and stopped forming after four months.

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

The four patients have a unique type of ichthyosis affecting hair follicles.

A rare calcium deposit condition was found on a man's scalp.

Intracorneal vacuoles are common in parakeratotic skin diseases in dogs, especially with more parakeratosis.

"D-CHRAMPS syndrome" is a newly identified condition with multiple severe symptoms.

A new mutation in the K6b gene caused a girl's late-appearing nail condition.

Sheet formation is key to macrofibril structure differences in wool.

PCFCL may have unrecognized subtypes and needs more research.

Trichogerminoma is a rare, benign skin tumor from hair cells, with a small risk of becoming cancerous.

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

A man with rare skin changes on his fingers was diagnosed with multiple myeloma-linked amyloidosis.

A patient with a PLEC mutation has epidermolysis bullosa, muscular dystrophy, and myasthenia gravis, which improved with steroid treatment.

A wide range of proteins are integrated into the skin's protective layer.

The patient has a rare skin condition that shows features of two known disorders.

Trichocytic cytokeratins are found in hair, nails, tongue, and thymus cells, showing complex regulation in tissue development.

A patient with Rothmund-Thomson syndrome showed skin changes, hair loss, and dental defects but no cataracts or skeletal issues.

Hereditary elliptocytosis causes elongated red blood cells and can lead to mild or no symptoms.

Follicular mucinosis causes significant damage to hair follicle cells.

Cronkhite-Canada syndrome can cause multiple gastrointestinal polyps and various physical symptoms.

Some canine hair follicle tumors contain amyloid deposits, with a protein called CK5 involved in their formation.

Brindled mice show abnormal catecholamine neuron development due to copper deficiency.

A boy had a rare scalp condition with thickened skin and different-colored hair.

Netherton's disease causes multiple hair defects.