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Titolo:
LHERMITTE-DUCLOS DISEASE - A CASE-REPORT
Autore:
HULCELLE P; DOOMS G; VERMONDEN J;
Indirizzi:
HOP JOLIMONT,SERV RADIOL,RUE FERRER B-7161 LA LOUVIERE BELGIUM CLIN UNIV ST LUC,DEPT IRM B-1200 BRUSSELS BELGIUM AIRC B-6060 GILLY BELGIUM
Titolo Testata:
Journal of neuroradiology
fascicolo: 1, volume: 21, anno: 1994,
pagine: 40 - 45
SICI:
0150-9861(1994)21:1<40:LD-AC>2.0.ZU;2-6
Fonte:
ISI
Lingua:
ENG
Soggetto:
DYSPLASTIC GANGLIOCYTOMA; CEREBELLUM;
Keywords:
CEREBELLUM; LHERMITTE-DUCLOS DISEASE; DYSPLASTIC GANGLIOCYTOMA; MRI;
Tipo documento:
Note
Natura:
Periodico
Settore Disciplinare:
Science Citation Index Expanded
Science Citation Index Expanded
Citazioni:
20
Recensione:
Indirizzi per estratti:
Citazione:
P. Hulcelle et al., "LHERMITTE-DUCLOS DISEASE - A CASE-REPORT", Journal of neuroradiology, 21(1), 1994, pp. 40-45

Abstract

We report one case of histologically proved Lhermitte-Duclos disease. Suspected on the basis of CT and angiography, the pre-operative diagnosis has been confirmed by the characteristic features of the lesion on MRI: a unilateral posterior fossa mass, hyperintense on proton density and T2-weighted images, hypointense on T1-weighted images, non enhancing after Gd administration. The gyral pattern was preserved, but a specific thickening of cerebellar folia was demonstrated. Despite a good post-operative short term prognosis, recurrence may occur. With a better depiction of lesion limits, MRI could improve the surgical approach and reduce the risk of subtotal excision.

ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 24/11/20 alle ore 22:09:57