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超声检查发现的新生儿室管膜下囊肿:患病率、超声表现及临床意义。

Neonatal subependymal cysts detected by sonography: prevalence, sonographic findings, and clinical significance.

作者信息

Larcos G, Gruenewald S M, Lui K

机构信息

Department of Nuclear Medicine and Ultrasound, Westmead Hospital, New South Wales, Australia.

出版信息

AJR Am J Roentgenol. 1994 Apr;162(4):953-6. doi: 10.2214/ajr.162.4.8141023.

Abstract

OBJECTIVE

Cranial sonography in neonates occasionally shows subependymal cysts. These cysts may be due to a variety of pathologic disorders, but they also occur as an "isolated" condition without an obvious cause in some patients. Assessment of the clinical significance of these lesions has been difficult because of the limited duration of follow-up, the informal nature of neurodevelopmental evaluation, and the heterogeneous cohort of patients previously reported. Accordingly, the purposes of this study were to provide more complete and longer neurodevelopmental followup and to describe the prevalence and sonographic characteristics of isolated subependymal cysts detected on cranial sonograms in neonates.

MATERIALS AND METHODS

In a 4 1/2-year period, more than 4000 cranial sonograms were obtained at our institution. We retrospectively determined that 17 neonates (59 studies) had sonographic evidence of an isolated subependymal cyst. A high-resolution real-time mechanical sector transducer was used to obtain the sonograms. No subjects had clinical or sonographic evidence of intercurrent hemorrhage, infarct, infection, or congenital abnormalities. Neurodevelopmental outcome was independently determined. In particular, premature infants who weighed less than 1500 g at birth were longitudinally assessed by a multidisciplinary developmental team. A general quotient was derived in nine subjects by using the Griffith Mental Developmental Scales.

RESULTS

Subependymal cysts were often tear shaped, 2-11 mm in size, and located either at the caudothalamic groove or along the anterior aspect of the caudate nucleus. Most subjects (n = 15) who had the cysts were born prematurely (mean gestational age, 31 weeks; range, 25-34 weeks). Results of follow-up were available in 14 infants 2-41 months old (mean, 22 months; median, 21 months). Development was considered to be normal in 13 of the 14 subjects; one term infant referred because of mild dysmorphic features had a mild global delay. The general quotient for corrected age, determined in nine subjects, had a mean of 111 (range, 103-120; normal, > 83). Fifteen neonates had at least two cranial sonographic examinations. In seven patients, serial examinations showed that cysts had resolved or diminished in size (on average 23 weeks after the initial sonographic study). In the other eight, no change in the size of the cyst was observed, but the mean interval between the first and last sonograms was only 14 days.

CONCLUSION

Cranial sonograms of neonates occasionally show isolated subependymal cysts, usually in premature infants. In most cases, no serious neurodevelopmental complications occur. Many cysts resolve after a variable period.

摘要

目的

新生儿头颅超声检查偶尔会发现室管膜下囊肿。这些囊肿可能由多种病理疾病引起,但在一些患者中也会作为“孤立”情况出现,无明显病因。由于随访时间有限、神经发育评估的非正式性质以及先前报道的患者队列的异质性,对这些病变的临床意义进行评估一直很困难。因此,本研究的目的是提供更完整、更长时间的神经发育随访,并描述新生儿头颅超声检查发现的孤立性室管膜下囊肿的患病率和超声特征。

材料与方法

在4年半的时间里,我们机构获得了4000多份头颅超声检查图像。我们回顾性确定17例新生儿(59次检查)有孤立性室管膜下囊肿的超声证据。使用高分辨率实时机械扇形探头获取超声图像。所有受试者均无并发出血、梗死、感染或先天性异常的临床或超声证据。独立确定神经发育结局。特别是,对出生时体重小于1500g的早产儿由多学科发育团队进行纵向评估。9名受试者使用格里菲斯心理发育量表得出一般商数。

结果

室管膜下囊肿通常呈泪滴状,大小为2 - 11mm,位于丘脑尾状沟或尾状核前缘。大多数有囊肿的受试者(n = 15)为早产儿(平均胎龄31周;范围25 - 34周)。14名2 - 41个月大的婴儿(平均22个月;中位数21个月)有随访结果。14名受试者中有13名发育被认为正常;一名因轻度畸形特征转诊的足月儿有轻度全面发育迟缓。9名受试者校正年龄的一般商数平均为111(范围103 - 120;正常,> 83)。15名新生儿至少进行了两次头颅超声检查。7例患者的系列检查显示囊肿已消退或缩小(初次超声检查后平均23周)。另外8例中,囊肿大小无变化,但首次和末次超声检查之间的平均间隔仅为14天。

结论

新生儿头颅超声检查偶尔会发现孤立性室管膜下囊肿,通常见于早产儿。大多数情况下,不会发生严重的神经发育并发症。许多囊肿在一段可变时间后会消退。

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