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European Journal of Dermatology

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Hyperkeratotic 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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Authors
1 Department of Dermatology,
2 Department of Neurology,
University Hospital Zürich,
Gloriastrasse 31,
8091 Zürich,
Switzerland
3 Laboratoire de Cytogénétique,
APHP Hôpital Lariboisière,
Paris,
France

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 [...]