Supratentorial cavernous haemangiomas and epilepsy: a review of the literature and case series

被引:136
作者
Moran, NF [1 ]
Fish, DR [1 ]
Kitchen, N [1 ]
Shorvon, S [1 ]
Kendall, BE [1 ]
Stevens, JM [1 ]
机构
[1] Inst Neurol, Epilepsy Res Grp, London WC1N 3BG, England
关键词
cavernous haemangioma epilepsy; magnetic resonance imaging; treatment; haemorrhage;
D O I
10.1136/jnnp.66.5.561
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objectives-To characterise the clinical features and response to treatment of supratentorial cavernomas associated with epilepsy. Methods-A systematic review of the literature was carried out and a retrospective case series of patients with cavernoma diagnosed by MRI and/or histology was compiled. Patient selection biases in the literature review were reduced as far as possible by selection of unbiased publications. Results-In the literature, cavernomas were relatively less common in the frontal lobes. There were multiple cavernomas in 23% of cases. The main clinical manifestations were seizures (79%) and haemorrhage (16%). The annual haemorrhage rate was 0.7%. The outcome after excision was good with improvement in seizures in 92% of patients. In the case series the surgical outcome was less favourable, reflecting inclusion of a higher proportion of patients with inh actable epilepsy. In both the literature review and the case series, outcome was poorer in cases with a longer duration of seizures at the time of surgery. Conclusions-The good surgical results, particularly in cases treated earlier, and the significant cumulative haemorrhage rate, suggest that excision is the optimum treatment. However, these factors have not been examined prospectively and, despite the availability of several retrospective studies, the optimum treatment, particularly for non-intractable cases, will only be determined by a prospective study.
引用
收藏
页码:561 / 568
页数:8
相关论文
共 75 条
[1]   INTRACRANIAL AND ORBITAL CAVERNOUS ANGIOMAS - A REVIEW OF 74 SURGICAL CASES [J].
ACCIARRI, N ;
PADOVANI, R ;
GIULIONI, M ;
GAIST, G ;
ACCIARRI, R .
BRITISH JOURNAL OF NEUROSURGERY, 1993, 7 (05) :529-539
[2]   NATURAL-HISTORY OF INTRACRANIAL CAVERNOUS MALFORMATIONS [J].
AIBA, T ;
TANAKA, R ;
KOIKE, T ;
KAMEYAMA, S ;
TAKEDA, N ;
KOMATA, T .
JOURNAL OF NEUROSURGERY, 1995, 83 (01) :56-59
[3]   INTRACRANIAL CAVERNOUS ANGIOMA [J].
BARTLETT, JE ;
KISHORE, PRS .
AMERICAN JOURNAL OF ROENTGENOLOGY, 1977, 128 (04) :653-656
[4]   OCCULT CEREBROVASCULAR MALFORMATIONS - SERIES OF 18 HISTOLOGICALLY VERIFIED CASES WITH NEGATIVE ANGIOGRAPHY [J].
BECKER, DH ;
TOWNSEND, JJ ;
KRAMER, RA ;
NEWTON, TH .
BRAIN, 1979, 102 (JUN) :249-287
[5]  
Bertalanffy Helmut, 1992, Neurologia Medico-Chirurgica, V32, P659, DOI 10.2176/nmc.32.659
[6]   FAMILIAL CAVERNOUS ANGIOMAS [J].
BICKNELL, JM ;
CARLOW, TJ ;
KORNFELD, M ;
STOVRING, J ;
TURNER, P .
ARCHIVES OF NEUROLOGY, 1978, 35 (11) :746-749
[7]  
BIGGER DD, 1989, RUSSELL RUBINSTEINS, P730
[8]   Stereotactically guided cavernous malformation surgery [J].
BoecherSchwarz, HG ;
Grunert, P ;
Guenthner, M ;
Kessel, G ;
MuellerForell, W .
MINIMALLY INVASIVE NEUROSURGERY, 1996, 39 (02) :50-55
[9]   MANAGEMENT OF CEREBRAL CAVERNOUS ANGIOMAS IN CHILDREN PRESENTING WITH SEIZURES [J].
BUCKINGHAM, MJ ;
CRONE, KR ;
BALL, WS ;
BERGER, TS .
CHILDS NERVOUS SYSTEM, 1989, 5 (06) :347-349
[10]   Supratentorial cavernous malformations and epilepsy: seizure outcome after lesionectomy on a series of 35 patients [J].
Cappabianca, P ;
Alfieri, A ;
Maiuri, F ;
Mariniello, G ;
Cirillo, S ;
deDivitiis, E .
CLINICAL NEUROLOGY AND NEUROSURGERY, 1997, 99 (03) :179-183