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非洲黑人儿童发育迟缓的影像学表现:喀麦隆雅温得的一项医院为基础的研究。

Imaging of developmental delay in black African children: A hospital-based study in Yaoundé-Cameroon.

机构信息

University of Yaounde I Faculty of Medicine and Biomedical Sciences, Pediatrics; Yaounde Gynaeco-Obstetric and pediatric Hospital, pediatrics.

University of Yaounde I Faculty of Medicine and Biomedical Sciences.

出版信息

Afr Health Sci. 2023 Mar;23(1):686-692. doi: 10.4314/ahs.v23i1.73.

DOI:10.4314/ahs.v23i1.73
PMID:37545916
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10398464/
Abstract

BACKGROUND

The purpose of this study was to describe the anomalies observed on imaging for developmental delay in black African children.

METHODS

It was a descriptive cross-sectional study, which included children aged between 1 month to 6 years with developmental delay and had done a brain MRI and/or CT scan.

RESULTS

We included 94 children, 60.6% of whom were males. The mean age was 32.5 ± 6.8 months. A history of perinatal asphyxia found in 55.3% of cases. According to the Denver developmental II scale, profound developmental delay observed in 35.1% of cases, and severe developmental delay in 25.5%. DD was isolated in 2.1% of cases and associated with cerebral palsy, pyramidal syndrome, and microcephaly in respectively 83%, 79.8%, and 46.8% of cases. Brain CT scan and MRI accounted for 85.1% and 14.9% respectively. The tests were abnormal in 78.7% of the cases, and cerebral atrophy was the preponderant anomaly (cortical atrophy = 80%, subcortical atrophy = 69.3%). Epileptic patients were 4 times more likely to have abnormal brain imaging (OR = 4.12 and p = 0.05),. We did not find a link between the severity of psychomotor delay and the presence of significant anomalies in imaging.

CONCLUSION

In our context, there is a high prevalence of organic anomalies in the imaging of psychomotor delay, which were dominated by cerebral atrophy secondary to hypoxic ischemic events.

摘要

背景

本研究旨在描述非洲黑人儿童发育迟缓的影像学表现。

方法

这是一项描述性的横断面研究,纳入了年龄在 1 个月至 6 岁之间、伴有发育迟缓且已行脑部 MRI 和/或 CT 扫描的儿童。

结果

共纳入 94 名儿童,其中 60.6%为男性,平均年龄为 32.5 ± 6.8 个月。55.3%的患儿有围产期窒息史。根据丹佛发育 II 量表,35.1%的患儿存在严重发育迟缓,25.5%的患儿存在重度发育迟缓。2.1%的患儿孤立性发育迟缓,分别有 83%、79.8%和 46.8%的患儿合并脑瘫、锥体外系综合征和小头畸形。脑 CT 扫描和 MRI 的检出率分别为 85.1%和 14.9%。78.7%的患儿检查结果异常,以脑萎缩为主(皮质萎缩=80%,皮质下萎缩=69.3%)。癫痫患儿脑影像学异常的可能性是正常患儿的 4 倍(OR=4.12,p=0.05)。我们未发现精神运动迟缓的严重程度与影像学异常之间存在关联。

结论

在我们的环境中,精神运动迟缓患儿的影像学检查存在较高的器质性异常发生率,以缺氧缺血性事件继发的脑萎缩为主。

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