Dandy-Walker Phenotype with Brainstem Involvement: 2 Distinct Subgroups with Different Prognosis.

IF 3.1 3区 医学 Q2 CLINICAL NEUROLOGY American Journal of Neuroradiology Pub Date : 2023-10-01 Epub Date: 2023-08-17 DOI:10.3174/ajnr.A7967
C A P F Alves, J Sidpra, A Manteghinejad, S Sudhakar, F V Massey, K A Aldinger, P Haldipur, L T Lucato, S F Ferraciolli, S R Teixeira, Ö Öztekin, D Bhattacharya, A Taranath, S P Prabhu, D M Mirsky, S Andronikou, K J Millen, A J Barkovich, E Boltshauser, W B Dobyns, M J Barkovich, M T Whitehead, K Mankad
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Abstract

Background and purpose: Although cardinal imaging features for the diagnostic criteria of the Dandy-Walker phenotype have been recently defined, there is a large range of unreported malformations among these patients. The brainstem, in particular, deserves careful attention because malformations in this region have potentially important implications for clinical outcomes. In this article, we offer detailed information on the association of brainstem dysgenesis in a large, multicentric cohort of patients with the Dandy-Walker phenotype, defining different subtypes of involvement and their potential clinical impact.

Materials and methods: In this established multicenter cohort of 329 patients with the Dandy-Walker phenotype, we include and retrospectively review the MR imaging studies and clinical records of 73 subjects with additional brainstem malformations. Detailed evaluation of the different patterns of brainstem involvement and their potential clinical implications, along with comparisons between posterior fossa measurements for the diagnosis of the Dandy-Walker phenotype, was performed among the different subgroups of patients with brainstem involvement.

Results: There were 2 major forms of brainstem involvement in patients with Dandy-Walker phenotype including the following: 1) the mild form with anteroposterior disproportions of the brainstem structures "only" (57/73; 78%), most frequently with pontine hypoplasia (44/57; 77%), and 2) the severe form with patients with tegmental dysplasia with folding, bumps, and/or clefts (16/73; 22%). Patients with severe forms of brainstem malformation had significantly increased rates of massive ventriculomegaly, additional malformations involving the corpus callosum and gray matter, and interhemispheric cysts. Clinically, patients with the severe form had significantly increased rates of bulbar dysfunction, seizures, and mortality.

Conclusions: Additional brainstem malformations in patients with the Dandy-Walker phenotype can be divided into 2 major subgroups: mild and severe. The severe form, though less prevalent, has characteristic imaging features, including tegmental folding, bumps, and clefts, and is directly associated with a more severe clinical presentation and increased mortality.

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脑干受累的Dandy Walker表型:2个不同预后的亚组。
背景和目的:尽管最近已经确定了Dandy Walker表型诊断标准的主要影像学特征,但这些患者中有大量未报告的畸形。脑干尤其值得注意,因为该区域的畸形对临床结果有潜在的重要影响。在这篇文章中,我们提供了一个大型、多中心的Dandy Walker表型患者队列中脑干发育不全相关性的详细信息,定义了不同的受累亚型及其潜在的临床影响。材料和方法:在这个由329名Dandy Walker表型患者组成的多中心队列中,我们纳入并回顾性回顾了73名额外脑干畸形受试者的MR成像研究和临床记录。对脑干受累的不同模式及其潜在临床意义进行了详细评估,并对诊断Dandy Walker表型的后颅窝测量值进行了比较。结果:Dandy Walker表型的患者有两种主要的脑干受累形式,包括以下几种:1)轻度脑干结构“仅”前后不均衡(57/73;78%),最常见的是脑桥发育不全(44/57;77%);2)重度脑干结构异常伴折叠、隆起和/或裂隙的患者(16/73;22%)。患有严重脑干畸形的患者出现大量脑室扩大、涉及胼胝体和灰质的其他畸形以及半球间囊肿的几率显著增加。临床上,严重型患者的延髓功能障碍、癫痫发作和死亡率显著增加。结论:Dandy Walker表型患者的额外脑干畸形可分为2个主要亚组:轻度和重度。严重型虽然不太常见,但具有特征性的影像学特征,包括被盖折叠、肿块和裂隙,并与更严重的临床表现和死亡率增加直接相关。
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来源期刊
CiteScore
7.10
自引率
5.70%
发文量
506
审稿时长
2 months
期刊介绍: The mission of AJNR is to further knowledge in all aspects of neuroimaging, head and neck imaging, and spine imaging for neuroradiologists, radiologists, trainees, scientists, and associated professionals through print and/or electronic publication of quality peer-reviewed articles that lead to the highest standards in patient care, research, and education and to promote discussion of these and other issues through its electronic activities.
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