Phacomatosis pigmentokeratotica (PP) is a mosaic disorder that represents a distinct epidermal naevus syndrome. Its defining features are an epidermal naevus that is usually of the sebaceous type and a speckled lentiginous naevus arranged in a chequerboard pattern. In addition, there are neurological, ophthalmological and skeletal abnormalities, including limb hemiatrophy with muscular weakness, ptosis, seizures and ipsilateral segmental hyperaesthesia and hyperhidrosis. We report a 44-year-old man with an extensive epidermal naevus and an ipsilateral speckled lentiginous naevus. He also had ipsilateral right leg hypertrophy and a suprasellar dermoid cyst with associated neurological abnormalities. We propose that this case represents an unusual example of PP. © 2007 The Author(s).
CITATION STYLE
Majmudar, V., Loffeld, A., Happle, R., & Salim, A. (2007). Phacomatosis pigmentokeratotica associated with a suprasellar dermoid cyst and leg hypertrophy. Clinical and Experimental Dermatology, 32(6), 690–692. https://doi.org/10.1111/j.1365-2230.2007.02511.x
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