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Titolo:
DYSPLASTIC GANGLIOCYTOMA OF THE CEREBELLUM (LHERMITTE-DUCLOS DISEASE)
Autore:
RAINOV NG; HOLZHAUSEN HJ; BURKERT W;
Indirizzi:
MASSACHUSETTS GEN HOSP E,DEPT MOLEC NEUROGENET,13TH ST,BLDG 149,6TH FL BOSTON MA 02129 UNIV HALLE WITTENBERG,FAC MED,DEPT NEUROSURG D-06097 HALLE GERMANY UNIV HALLE WITTENBERG,FAC MED,INST PATHOL ANAT HALLE GERMANY
Titolo Testata:
Clinical neurology and neurosurgery
fascicolo: 2, volume: 97, anno: 1995,
pagine: 175 - 180
SICI:
0303-8467(1995)97:2<175:DGOTC(>2.0.ZU;2-V
Fonte:
ISI
Lingua:
ENG
Soggetto:
COWDEN DISEASE; IMMUNOHISTOCHEMISTRY; DIAGNOSIS; MRI;
Keywords:
COWDEN SYNDROME; DYSPLASTIC GANGLIOCYTOMA; LHERMITTE-DUCLOS DISEASE;
Tipo documento:
Note
Natura:
Periodico
Settore Disciplinare:
Science Citation Index Expanded
Science Citation Index Expanded
Citazioni:
29
Recensione:
Indirizzi per estratti:
Citazione:
N.G. Rainov et al., "DYSPLASTIC GANGLIOCYTOMA OF THE CEREBELLUM (LHERMITTE-DUCLOS DISEASE)", Clinical neurology and neurosurgery, 97(2), 1995, pp. 175-180

Abstract

The case of a 30-year-old male patient is presented who was admitted with a 3-month history of elevated intracranial pressure and reduced-hearing on the right. CT revealed hydrocephalus due to displacement of the 4th ventricle by a large non-enhancing cerebellar mass with calcifications. MRI sequences showed a space-occupying lesion within the right cerebellar hemisphere with unusual septations. At operation, the poorly demarcated lesion was excised from the apparently normal surrounding cerebellar tissue and histologically proven to be a dysplastic gangliocytoma (Lhermitte-Duclos disease). Clinical and neuroradiological appearance of this rare entity, as well as hypotheses on its pathogenesis are discussed.

ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 24/11/20 alle ore 11:26:30