Lin J P, Goh W, Brown J K, Steers A J
Department of Paediatric Neurology, Royal Hospital for Sick Children, Edinburgh, UK.
Childs Nerv Syst. 1993 Jul;9(4):205-14. doi: 10.1007/BF00303571.
To evaluate the topographical neurological distribution, patterns of abnormal tone and related functional neuromotor impairment after grade 3 and grade 4 intraventricular/periventricular haemorrhage (IPVH), 33 children with previous grade 3 or 4 IPVH of mean gestational age 30.9 weeks (range 25-40 weeks) and mean birth weight 1743 g (range 866-3600 g) were examined neurologically at 4.7 years (range 0.75-10.8 years). Neurological signs were absent in 10/33 cases which were equally distributed between the grade 3 and grade 4 IPVH groups. The largest single topographical neurological distribution was hemiparesis in 8/23, followed jointly by diplegia (cerebral paraplegia) in 6/23 and triplegia in 6/23 cases and finally quadriplegia in 3/23 cases. Grade 4 IPVH tended to result in asymmetrical syndromes, accounting for 7/8 cases of hemiparesis and 5/6 cases of triplegia, whereas all 3/3 cases of quadriplegia followed grade 3 IPVH. The 6/23 cases of diplegia were shared between the grade 3 and grade 4 IPVH groups. Tone was normal in 7/8 of the hemiparetic subjects. Dystonia was the commonest tone abnormality, affecting 8/23 children with neurological disturbance, followed by ataxia/hypotonia in 4/23 and mixed dystonia/hypotonia in 3/23. Only 1/23 cases had signs of spasticity. Spasticity is rare following severe IPVH. Diplegic children had a better functional neuromotor grade than hemiparetic children, who in turn did better than triplegic children. Ataxia hypotonia resulted in better functional outcome than dystronia, which in turn was more favourable than mixed tone patterns. Cranial imaging by ultrasound (US) or computed tomographic (CT) scanning proved an unreliable prognostic indicator except in the case of hemiparesis, for which US scans correctly predicted the affected side in 5/7 cases. The neurological syndromes following severe IPVH differ from the classical encephalopathy of prematurity, and this should lead to a re-appraisal of the trends in the prevalence of cerebral palsy. Caution should be exercised in the interpretation of cranial imaging with regard to pessimistic prognoses in the presence of changes or undue optimism in their absence.
为评估3级和4级脑室内/脑室周围出血(IPVH)后神经功能的局部分布、异常肌张力模式及相关功能性神经运动障碍,对33例曾患3级或4级IPVH的儿童进行了神经学检查,这些儿童的平均胎龄为30.9周(范围25 - 40周),平均出生体重为1743克(范围866 - 3600克),检查时间为4.7岁(范围0.75 - 10.8岁)。33例中有10例无神经学体征,在3级和4级IPVH组中分布均匀。最大的单一局部神经功能分布是偏瘫,23例中有8例;其次是双侧瘫(脑性截瘫)和三肢瘫,各有6例;最后四肢瘫有3例。4级IPVH倾向于导致不对称综合征,占偏瘫病例的7/8和三肢瘫病例的5/6,而所有3例四肢瘫均继发于3级IPVH。23例中有6例双侧瘫在3级和4级IPVH组中均有。偏瘫患者中有7/8肌张力正常。肌张力障碍是最常见的肌张力异常,23例有神经功能障碍的儿童中有8例受影响,其次是共济失调/低张力4例,肌张力障碍/低张力混合3例。23例中只有1例有痉挛体征。重度IPVH后痉挛罕见。双侧瘫儿童的功能性神经运动分级优于偏瘫儿童,偏瘫儿童又优于三肢瘫儿童。共济失调低张力导致的功能结局优于肌张力障碍,肌张力障碍又比混合性肌张力模式更有利。超声(US)或计算机断层扫描(CT)的头颅成像被证明是不可靠的预后指标,除了偏瘫情况,对于偏瘫,超声扫描在7例中有5例正确预测了患侧。重度IPVH后的神经综合征与经典的早产儿脑病不同,这应该促使对脑瘫患病率趋势进行重新评估。在解读头颅成像时,对于有改变时的悲观预后或无改变时的过度乐观都应谨慎。