Search

everythingexperts & clinicslearnresearchcommunity

for

Search:↓

Trichofolliculoma was found in a person with amniotic band syndrome for the first time.

Tinea faciei should be considered in neonatal vesicular lesions and confirmed with KOH examination and culture.

A rare case of hair loss was linked to breast cancer spreading to the scalp, but treatment was effective.

Recognizing trichofolliculomas is important to avoid unnecessary surgery.

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

NISCH syndrome is a rare genetic disorder affecting skin and liver, with variable symptoms and limited treatment options.

Nail disorders not caused by infection are common and can look similar, with psoriasis being the most frequent and having specific nail symptoms.

Reflectance confocal microscopy can noninvasively diagnose onychomatricoma by showing unique features different from healthy nails or nail fungus.

A rare skin cancer was correctly diagnosed after surgery, highlighting the need for careful examination and follow-up.

A woman had a rare skin condition with recurring painful nodules that heal in 6 weeks, often without needing treatment.

Keratoacanthoma and some squamous cell carcinomas are linked to hair follicles, while others are not.

Vitiligo causes white skin patches, often starts before age 20, and is linked to other health issues.

A new genetic mutation in the ODC1 gene causes developmental delay and other symptoms in a young girl.

Neuroendocrine paraneoplastic syndromes often show skin changes, helping early diagnosis and requiring a team approach for best care.

Skin changes like hair loss, white patches, and nail changes are common in children after bone marrow transplants, often linked to chronic rejection.

Keratin 15 cells from hair follicles help develop and maintain skin tumors in mice.

Recognizing IPPP is crucial to prevent misdiagnosis and unnecessary treatments.

Scalp pemphigus vulgaris can be effectively treated with low-dose prednisone and triamcinolone.

Some immunosuppressed patients can get unusual skin infections from Malassezia, which can be treated with antifungal medication.

Podiatrists need more training to detect foot melanoma early.

Erythromelanosis follicularis faciei can also affect women, though it's rare.

The patient has a leg condition caused by vein issues, needing lifestyle changes and leg care.

Nail changes from immunotherapy can be managed without stopping cancer treatment.

Nail issues are common in kids with alopecia areata and should be checked for better diagnosis.

Giant keratoacanthoma can look like squamous cell carcinoma, requiring careful diagnosis and surgical removal.

Neuropilin 2 may be a biomarker for melanoma and affects melanocyte behavior.

Familial dyskeratotic comedones are a rare, inherited skin condition that is hard to treat but may improve slightly with topical retinoids and urea cream.

Trichilemmoma, BCC, and SCC tumors have different stem cell marker expressions.

Patients with Focal Dermal Hypoplasia often experience skin, nail, hair, and bone issues, and may benefit from calcium and vitamin D supplements.