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磁共振成像模式下亚急性硬化性全脑炎可能类似于代谢紊乱:6 例临床、脑电图和影像学特征。

Magnetic resonance imaging patterns of subacute sclerosing panencephalitis may mimic metabolic disorders: clinical, electroencephalographic and imaging features of six cases.

机构信息

Department of Pediatric Neurology, Faculty of Medicine, Gazi University, Besevler, 06510, Ankara, Turkey.

Department of Pediatric Neurology, Hatay State Hospital, Antakya, Hatay, Turkey.

出版信息

Acta Neurol Belg. 2021 Aug;121(4):955-965. doi: 10.1007/s13760-020-01469-1. Epub 2020 Aug 18.

DOI:10.1007/s13760-020-01469-1
PMID:32809122
Abstract

Subacute sclerosing panencephalitis is a rare, devastating neurodegenerative encephalitis whose diagnosis and therapy are still in question. Atypical clinical presentation and heterogeneity of neuroimaging findings that have been initially confused with metabolic disorders have hampered early diagnosis. To describe a series of patients with subacute sclerosing panencephalitis with imaging findings mimicking metabolic disorders. A total of six patients with subacute sclerosing panencephalitis were diagnosed from January 2012 to December 2016 in whom a metabolic disorder was suspected on initial clinical and MRI findings. Detailed laboratory investigation was performed in all patients. All patients presented with atypical neurologic manifestations, including dystonia, syncopal attacks, involuntary limb movements, meaningless speech and ataxia. Magnetic resonance imaging abnormalities included bilateral putaminal, bilateral posterior periventricular white matter and diffuse or splenial corpus callosum involvement which are particularly unusual in SSPE and mostly observed in metabolic disorders. All patients had elevated cerebrospinal fluid Ig G measles antibodies. The diagnosis of subacute sclerosing panencephalitis through clinical and imaging features can be considerably challenging. It is crucial to differentiate it from metabolic disorders, since the management and clinical outcome are different.

摘要

亚急性硬化性全脑炎是一种罕见且具有破坏性的神经退行性脑炎,其诊断和治疗仍存在疑问。不典型的临床表现和神经影像学表现的异质性,最初与代谢紊乱相混淆,这阻碍了早期诊断。描述一组影像学表现类似于代谢紊乱的亚急性硬化性全脑炎患者。2012 年 1 月至 2016 年 12 月期间,共诊断出 6 例亚急性硬化性全脑炎患者,这些患者在最初的临床和 MRI 发现中怀疑存在代谢紊乱。对所有患者均进行了详细的实验室检查。所有患者均表现出非典型的神经表现,包括肌张力障碍、晕厥发作、不自主肢体运动、无意义言语和共济失调。磁共振成像异常包括双侧壳核、双侧侧脑室周围白质和弥漫性或胼胝体压部受累,这在 SSPE 中特别不常见,主要见于代谢紊乱。所有患者的脑脊液 IgG 麻疹抗体升高。通过临床和影像学特征诊断亚急性硬化性全脑炎具有相当大的挑战性。与代谢紊乱相鉴别非常重要,因为其治疗和临床结局不同。

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Am J Trop Med Hyg. 2023 Mar 13;108(5):1025-1027. doi: 10.4269/ajtmh.22-0731. Print 2023 May 3.

本文引用的文献

1
Subacute sclerosing panencephalitis: evaluation with CT and MR.亚急性硬化性全脑炎:CT与MR评估
AJNR Am J Neuroradiol. 1996 Apr;17(4):761-72.