Wilkinson I, Bear J, Smith J, Gill A, Challinor C, Jones W, Shahidullah M, Wooderson S
John Hunter Hospital, Newcastle, New South Wales, Australia.
J Paediatr Child Health. 1996 Oct;32(5):445-9. doi: 10.1111/j.1440-1754.1996.tb00947.x.
To determine the neurological outcome of a cohort of premature babies having ultrasound diagnoses of severe cystic periventricular leukomalacia.
All neonatal intensive care unit admissions born at less than 35 weeks gestation or weighing less than 1500 g underwent serial cranial ultrasounds. Those developing severe bilateral cystic periventricular leukomalacia (12 patients) were then followed clinically to a mean age of 27.3 months.
Ten of the 12 patients fulfilling strict ultrasound criteria survived. All had a major neurological handicap, all having spastic quadriparesis and visual impairments, with most suffering global developmental delay and epilepsy.
Severe bilateral cystic periventricular leukomalacia results in major permanent handicap. It is currently impossible to identify most patients with this condition while they are being ventilated. Non-ultrasound techniques are needed to diagnose the condition earlier, and to give guidance to management.
确定一组经超声诊断为重度囊性脑室周围白质软化症的早产儿的神经学转归。
所有孕周小于35周或出生体重小于1500克的新生儿重症监护病房入院患儿均接受了系列头颅超声检查。随后对出现重度双侧囊性脑室周围白质软化症的患儿(12例)进行临床随访,直至平均年龄达27.3个月。
符合严格超声标准的12例患儿中有10例存活。所有患儿均有严重神经功能障碍,均表现为痉挛性四肢瘫和视力障碍,多数患儿存在全面发育迟缓及癫痫。
重度双侧囊性脑室周围白质软化症会导致严重的永久性残疾。目前在患儿接受机械通气时,多数患有此病的患儿无法被识别。需要采用非超声技术更早地诊断此病,并为治疗提供指导。