Diagnostic imaging in 13 cases of Rasmussen's encephalitis: can early MRI suggest the diagnosis?

被引:98
作者
Chiapparini, L
Granata, T
Farina, L
Ciceri, E
Erbetta, A
Ragona, F
Freri, E
Fusco, L
Gobbi, G
Capovilla, G
Tassi, L
Giordano, L
Viri, M
Dalla Bernardina, B
Spreafico, R
Savoiardo, M
机构
[1] Inst Nazl Neurol C Besta, Dept Neuroradiol, I-20133 Milan, Italy
[2] Ist Nazl Neurol Carlo Besta, Dept Paediat Neurol, Milan, Italy
[3] Osped Pediat Bambino Gesu, Dept Paediat Neurol, Rome, Italy
[4] Osped Maggiore Pizzardi, Dept Paediat Neurol, Bologna, Italy
[5] Osped Poma, Dept Paediat Neurol, Mantua, Italy
[6] Osped Niguarda Ca Granda, Dept Epilepsy Surg, Milan, Italy
[7] Osped Fatebenefratelli Oftalmico, Epilepsy Ctr, Milan, Italy
[8] Osped Civile, Dept Paediat Neurol, Brescia, Italy
关键词
Rasmussen's encephalitis; epilepsia partialis continua; magnetic resonance imaging;
D O I
10.1007/s00234-002-0923-7
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Rasmussen's encephalitis (RE) is a rare, progressive, chronic encephalitis characterised by drugresistant epilepsy, progressive hemiparesis and mental impairment. It typically involves only one cerebral hemisphere, which becomes atrophic. We present neuroradiological findings in 13 children with RE. MRI was performed in all patients, fluorodeoxyglucose positron-emission tomography (PET) in three, Tc-99m hexamethylpropylenamine oxime single-photon emission computed tomography (SPECT) in two and proton MR spectroscopy ((HMRS)-H-1) in two. MRI showed progression of the hemisphere atrophy, always prevalent in the region primarily involved (13 patients), spread of the abnormal signal in white matter (11) and cortex (10) and progression of atrophy of the head of the caudate nucleus (nine). Associated secondary changes were: atrophy of the contralateral cerebellar hemisphere (in four patients), the ipsilateral hippocampus (in five) and the brain stem (in five). The earliest CT and MRI abnormalities, seen between I day and 4 months after the first seizure (in 12 patients examined, nine of whom had MRI) in one cerebral hemisphere included: high signal on T2-weighted images in the cortex (seven patients) and white matter (nine), cortical atrophy usually involving the frontoinsular region, with mild or severe enlargement of the lateral ventricle (eight) and moderate atrophy of the head of the caudate nucleus (seven). Cortical swelling in the early stage of the disease was recognisable only in two patients. PET revealed hypometabolism, SPECT decreased perfusion, and (HMRS)-H-1 reduction of N-acetylaspartate in the affected hemisphere. PET and SPECT were usually performed in the late stages and did not provide specific findings. MRI thus demonstrates the progression of RE and may suggest the diagnosis in the early stages, often before the appearance of neurological deficits. Early diagnosis of RE may be crucial for selecting patients for aggressive medical therapy or major surgical interventions such as hemispherectomy.
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收藏
页码:171 / 183
页数:13
相关论文
共 41 条
[1]  
[Anonymous], CHRONIC ENCEPHALITIS
[2]  
ATLAS SW, 1996, MAGNETIC RESONANCE I, P707
[3]   [11C](R)-PK11195 positron emission tomography imaging of activated microglia in vivo in Rasmussen's encephalitis [J].
Banati, RB ;
Goerres, GW ;
Myers, R ;
Gunn, RN ;
Turkheimer, FE ;
Kreutzberg, GW ;
Brooks, DJ ;
Jones, T ;
Duncan, JS .
NEUROLOGY, 1999, 53 (09) :2199-2203
[4]  
BARKOVICH AJ, 2000, PEDIAT NEUROIMAGING, P744
[5]   Rasmussen's encephalitis: Neuroimaging findings in 21 patients with a closer look at the basal ganglia [J].
Bhatjiwale, MG ;
Polkey, C ;
Cox, TCS ;
Dean, A ;
Deasy, N .
PEDIATRIC NEUROSURGERY, 1998, 29 (03) :142-148
[6]   Diagnosis and staging of Rasmussen's encephalitis by serial MRI and histopathology [J].
Bien, CG ;
Urbach, H ;
Deckert, M ;
Schramm, J ;
Wiestler, OD ;
Lassmann, H ;
Elger, CE .
NEUROLOGY, 2002, 58 (02) :250-257
[7]   The natural history of Rasmussen's encephalitis [J].
Bien, Christian G. ;
Widman, Guido ;
Urbach, Horst ;
Sassen, Robert ;
Kuczaty, Stefan ;
Wiestler, Otmar D. ;
Schramm, Johannes ;
Elger, Christian E. .
BRAIN, 2002, 125 :1751-1759
[8]   EARLY DETECTION OF RASMUSSEN SYNDROME BY BRAIN SPECT IMAGING [J].
BURKE, GJ ;
FIFER, SA ;
YODER, J .
CLINICAL NUCLEAR MEDICINE, 1992, 17 (09) :730-731
[9]   IMAGING OF AXONAL DAMAGE IN-VIVO IN RASMUSSENS SYNDROME [J].
CENDES, F ;
ANDERMANN, F ;
SILVER, K ;
ARNOLD, DL .
BRAIN, 1995, 118 :753-758
[10]   REAPPRAISAL OF RASMUSSENS-SYNDROME WITH SPECIAL EMPHASIS ON TREATMENT WITH HIGH-DOSES OF STEROIDS [J].
CHINCHILLA, D ;
DULAC, O ;
ROBAIN, O ;
PLOUIN, P ;
PONSOT, G ;
PINEL, JF ;
GRABER, D .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 1994, 57 (11) :1325-1333