European Journal of Dermatology
MENUHyperkeratotic cutaneous vascular malformation associated with familial cerebral cavernous malformations (FCCM) with KRIT1/CCM1 mutation Volume 24, issue 2, March-April 2014
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1 Department of Dermatology,
- DOI : 10.1684/ejd.2014.2280
- Page(s) : 255-7
- Published in: 2014
We report the case of a 40-year-old male patient with a history of seizures due to multiple cerebral cavernomas since the age of 14, treated by oxycarbamazepine and lamotrigine. Familial history for cerebral cavernomas was negative. The patient was referred to the department of Dermatology by his neurologist for the evaluation of an asymptomatic dark-blue spot on the left heel, which had been present for many years. The lesion was an isolated well-delimited dark-blue hyperkeratotic plaque with an [...]