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Steatocystoma multiplex causes recurring skin cysts and needs early recognition for better management.

Cathepsin L deficiency causes large, abnormal cell structures and health issues in mice.

A rare skin condition was misdiagnosed as a harmless mole on a woman's eyelid.

A painless cheek lump was misdiagnosed but found to be a rare, benign skin lesion called pilomatrixoma, treatable by surgery.

A rare hair follicle tumor showed unusual high levels of mucin.

Hair repigmentation can indicate malignancy and should be investigated.

Steroid treatment improved both gut and nerve symptoms in a man with Cronkhite–Canada syndrome.

PCFCL may have unrecognized subtypes and needs more research.

A rare adrenal tumor in a 9-year-old girl was successfully treated with surgery.

Generalized trichoepitheliomas with hair loss may indicate myasthenia gravis.

A painless cheek lump was misdiagnosed but later identified as a rare benign skin lesion called pilomatrixoma.

Consider Castleman's disease in similar cases; histology and steroids help diagnose and manage it.

Bone marrow-derived cells contribute to skin tumors, suggesting new treatment targets for non-melanoma skin cancers.

The study suggests that mast cells might be involved in the hair loss condition telogen effluvium and could be a target for treatment.

CYLD deficiency in skin tumors disrupts hair follicle cell processes and protein secretion.

Waldenstrom’s Macroglobulinaemia can mimic multiple myeloma, so accurate diagnosis is crucial.

A skin condition called pyodermatitis vegetans was found in a patient with multiple myeloma for the first time.

Albumin and prednisone improved symptoms in a woman with Cronkhite-Canada syndrome, revealing potential genetic causes.

Basal cell carcinoma with matrical differentiation is a rare type linked to hair follicles, with .-catenin important for its development.

Benign follicular mucinosis involves immune cells attacking hair follicles.

Mitochondriopathy may cause eyelash loss.

Acneiform follicular mucinosis can be controlled with systemic corticosteroids.

Recognizing minor skin lesions can help identify serious cancer syndromes.

A woman's cyclic Cushing syndrome was caused by a tumor in her adrenal gland that produced ACTH.

Cronkhite-Canada syndrome is rare, with high mortality and cancer risk, needing more research for treatment guidelines.

The boy's symptoms suggest a possible new medical condition.

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

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

Malassezia in cat skin biopsies may indicate internal cancer.

A man had a non-cancerous, fast-growing skin lump on his arm that was removed with surgery.