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Clinico-neuropathological study of incontinentia pigmenti achromians — an autopsy case
Authors:Osamu Fujino   Kiyoshi Hashimoto   Takehisa Fujita   Hisashi Enokido   Hideki Komatsuzaki   Goro Asano   Junichi Sato  Yoshio Morimatsu
Affiliation:

aDepartment of Pediatrics, Nippon Medical School, 1-1-5 Sendagi, Bunkyo-ku, Tokyo 113, Japan

bDepartment of Pathology, Nippon Medical School, Tokyo, Japan

cDivision of Clinical Neuropathology, Tokyo Metropolitan Institute for Neurosciences, Tokyo, Japan

Abstract:
A clinico-neuropathological study of a Japanese girl with hypomelanosis of Ito, one of the neurocutaneous syndromes, is reported. At birth, typical skin hypopigmentation on the trunk and a hypopigmented streak on the left lower extremity were noted. From 2 months of age, intractable convulsions occured and EEG showed various abnormalities. Psychomotor development was severely retarded and she died of pneumonia at the age of 13 months. Neuropathological examination revealed brachycephaly, micropolygyria and asymmetry of lateral ventricles. A histological examination showed a disarray of cortical lamination, and the existence of nerve cells in the white matter. These pathological findings showed a migration anomaly during brain maturation.
Keywords:Hypomelanosis of Ito (incontinentia pigmenti achromians)   Micropolygyria   Gray matter heterotopia   Intractable seizure
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