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Pigmented papules on the ear can be a rare skin condition called cutaneous amyloidosis, treatable with topical tretinoin.

The document concludes that ERBB2 mutations are common in extramammary Paget disease and may respond to systemic treatments like cancer immunotherapy.

A 9-year-old boy had a calcium deposit nodule on his earlobe.

DPR can show different hair characteristics, as seen in two brothers with normal hair.

ALEP is a drug-triggered skin reaction with pustules that clears up in a week after stopping the drug.

Middle Eastern patients with epidermolysis bullosa show specific genetic mutations linked to different types of the disease.

Mutant keratins cause inflammation in Epidermolysis Bullosa Simplex, suggesting targeting them could help treat the disorder.

Corneal issues in pemphigus vulgaris may require surgery if medication is not followed.

A dark-haired Chinese girl had hair that looked banded under certain light but was normal under a microscope.

The study found clear differences in lesion distribution and microscopic features among trichostasis spinulosa, keratosis pilaris, and eruptive vellus hair cysts.

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

Molluscum contagiosum can occur in epidermoid cysts, especially with prolonged steroid use.

A heart transplant patient developed a skin condition called epidermodysplasia verruciformis after taking immune-suppressing drugs.

A rare benign tumor was found in a man's scrotum, highlighting the need for accurate diagnosis.

Cetuximab can cause eyelash growth, which is rare but manageable.

Nevus comedonicus is a rare skin condition with grouped open pores, sometimes linked to other body issues.

Nevus comedonicus can sometimes grow terminal hair, challenging previous beliefs.

Eyelid pilomatrixomas are rare, benign tumors that need accurate diagnosis for proper treatment.

Topical 6% salicylic acid effectively reduced skin plaques in a patient with wooly hair and palmoplantar keratoderma.

Spiny keratoderma is a rare skin condition with small spines on palms and soles, possibly linked to abnormal hair formation.

Dermatologists give better information on pathology forms, hypersensitivity vasculitis is a common skin issue, misdiagnoses can occur, and various skin conditions are linked to loss of elastin or genetic factors.

A bull with a gene mutation was asymptomatic, synthetic retinoids cause hair loss, and new therapeutic targets were identified for skin diseases.

The document reports unique growth lines in a child after Stevens-Johnson syndrome, skin reaction from parsnips and sun in a girl, and itchy skin with xanthomas in a boy with Alagille syndrome.

Restoring phenylalanine levels improved skin and hair symptoms in a PKU infant.

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

Pseudopelade of Brocq is hard to diagnose and treat, with limited effective options.

Accurate diagnosis of APL is crucial to avoid unnecessary treatments.

Prurigo pigmentosa mainly affects middle-aged White and Asian women, often linked to a ketogenic diet, and is best treated with oral antibiotics.

Erosive pustular dermatosis of the scalp can occur about 17 weeks after starting EGFR inhibitors, and early minocycline may help manage it.