Cowden syndrome
Trichilemmomas in Cowden syndrome
Keywords: Cowden disease, Cowden syndrome, Autosomal dominant genetic disorder, Cheek, Face, Keratotic papules, Multiple hamartoma syndrome, Multiple skin-coloured papules, Skin of colour, Trichilemmoma
What is Cowden syndrome?
Cowden syndrome is a rare, autosomal dominant, inherited condition characterised by hamartomas in various organs, including breast, thyroid, uterus, brain, and mucocutaneous tissues with increased risk of malignancies. It is also known as ‘Cowden disease’ or ‘multiple hamartoma syndrome’.
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