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Phakomatosis pigmentovascularis: A new case with renal angiomas and some considerations about the classification
A Di Landro1, G L Tadini, L Marchesi
1Clinica Dermatologica V, Universita' degli Studi di Milano, Bergamo General Hospital Bergamo, Italy.gonzer.caste@ctrade.it
Abstract:
We report phakomatosis pigmentovascularis detected in a Caucasian child characterized by the presence of a nevus flammeus and nevus anemicus on the face, a telangiectatic linear nevus of the right leg, and a very extensive blue spot covering 60% of the body surface, with ocular melanosis. Multiple angiomatous lesions of the kidney are associated without alterations of the central nervous system (CNS). This association has not been reported before; it could be a further expression of the complex of developmental defects. Our case corresponds exactly to type IIb in the classification of phakomatosis pigmentovascularis proposed by Hasegawa. As this classification seems very extensive, the higher incidence of cases corresponding to the second subtype suggests that we should identify it by the term phakomatosis pigmentovascularis, while the others could be considered as only very uncommon variants.
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