Bass W T, Jones M A, White L E, Montgomery T R, Aiello F, Karlowicz M G
Department of Pediatrics, Eastern Virginia Medical School, Norfolk, USA.
J Perinatol. 1999 Jul-Aug;19(5):330-6. doi: 10.1038/sj.jp.7200190.
To determine the clinical usefulness of recently published ultrasonographic criteria for the differential diagnosis of periventricular hemorrhagic venous infarction (PHVI) versus periventricular leukomalacia (PVL), and its relevance to neurodevelopmental outcome.
From 1992 to 1995, we evaluated 998 very low birth weight infants of which 111 developed cerebral white matter lesions on cranial ultrasonogram examination. An attempt was made to differentiate the lesions into either PHVI or PVL using specific ultrasonographic criteria (Volpe JJ. Brain inury in the premature infant: is it preventable? Pediatr Res 1990; 6:S28-33). Seventy-six patients who survived to discharge constituted the study group. Survivors were followed prospectively with neurologic examinations, visual and auditory screening, and developmental testing.
PHVI was diagnosed in 23 patients (30%), PVL in 36 (47%), characteristics of both PHVI and PVL (mixed lesions) in 8 (11%), and persistent periventricular echodensity without cystic change in 9 (12%). Two-year follow-up data were obtained on 57 of 76 (75%) patients. Neurodevelopmental deficits were common in all groups; however, infants with localized PHVI had a mean developmental quotient in the normal range.
The majority of white matter lesions (77%) can be differentiated as either PHVI or PVL by ultrasonographic criteria, with coexisting features in only 11% of patients. In addition to these lesions, persistent periventricular echodensity was also associated with a high risk of subsequent neurodevelopmental deficit. However, normal development was seen in a subgroup of patients with localized periventricular hemorrhagic venous infarction.
确定最近发表的超声诊断标准在鉴别脑室周围出血性静脉梗死(PHVI)与脑室周围白质软化(PVL)方面的临床实用性及其与神经发育结局的相关性。
1992年至1995年,我们评估了998例极低出生体重儿,其中111例在头颅超声检查时出现脑白质病变。尝试使用特定的超声诊断标准(Volpe JJ. 早产儿脑损伤:能否预防?儿科研究1990;6:S28 - 33)将这些病变区分为PHVI或PVL。76例存活至出院的患者组成研究组。对存活者进行前瞻性随访,包括神经学检查、视觉和听觉筛查以及发育测试。
23例(30%)诊断为PHVI,36例(47%)为PVL,8例(11%)具有PHVI和PVL的特征(混合性病变),9例(12%)为脑室周围持续回声增强且无囊性改变。76例患者中的57例(75%)获得了两年的随访数据。所有组中神经发育缺陷都很常见;然而,局限性PHVI的婴儿平均发育商在正常范围内。
大多数白质病变(77%)可通过超声诊断标准区分为PHVI或PVL,仅11%的患者存在共存特征。除这些病变外,脑室周围持续回声增强也与随后神经发育缺陷的高风险相关。然而,局限性脑室周围出血性静脉梗死患者亚组中可见正常发育情况。