From the Division of Neuropaediatrics (J.G.-A., A.M.), Hospital for Children and Adolescents, University Hospital Leipzig, Leipzig, Germany
Department of Pediatric Radiology (I.S.), University Hospital for Children and Adolescents, University Leipzig, Germany.
AJNR Am J Neuroradiol. 2023 Sep;44(9):1090-1095. doi: 10.3174/ajnr.A7948. Epub 2023 Aug 24.
Despite its rarity in Western countries, kernicterus resulting from severe neonatal hyperbilirubinemia and its associated neurologic consequences still persists. Subtle MR imaging patterns may be overlooked, leading to diagnostic and prognostic uncertainties. The study systematically analyzes MR imaging pattern over time.
A retrospective MR imaging study was conducted in Departments of Pediatric Neurology at the University Children's Hospitals in Leipzig, Germany, or Tübingen, Germany, between 2012 and 2022 in patients who presented beyond the neonatal period suspected of having chronic kernicterus.
Eight patients with a total of 15 MR images were identified. The clinical diagnosis of kernicterus was confirmed in all cases on the basis of typical MR imaging findings: Bilateral, diffuse hyperintensity of the globus pallidus was observed in the neonatal period on T1WI (1 MR imaging, at 2 weeks), in infancy on T2WI (4 MR images, at 9-26 months). In children 2 years of age and older, bilateral hyperintensity on T2WI was limited to the borders of the globus pallidus (8 MR images, at 20 months -13 years). Notably, 2 children exhibited normal initial MR imaging findings at 2 months of age. Hence, MR imaging depiction of kernicterus pathology evolves with time, first evident on T1WI, subsequently on T2WI, with a "blind window" during early infancy. The T2WI signal change initially involves the entire globus pallidus and later is limited to the borders. Kernicterus had not been diagnosed in any except 2 patients by previous investigators.
All patients presented with a characteristic clinical history and signs and an evolving MR imaging pattern. Nonetheless, the diagnosis of kernicterus was frequently missed. Abnormalities on later MR images appear to be underrecognized.
尽管在西方国家较为罕见,但严重新生儿高胆红素血症引起的核黄疸及其相关神经后果仍然存在。细微的磁共振成像(MR)表现可能被忽视,导致诊断和预后不确定。本研究系统地分析了随时间推移的 MR 成像模式。
回顾性研究了 2012 年至 2022 年期间在德国莱比锡大学儿童医院或图宾根大学儿童医院神经科就诊的、怀疑患有慢性核黄疸的晚发性新生儿期患者的 MR 成像资料。
共确定了 8 例患者,共 15 个 MR 图像。所有病例均根据典型的 MR 成像表现确诊为核黄疸:在新生儿期 T1WI 上(1 个 MR 图像,2 周龄)观察到双侧苍白球弥漫性高信号,在婴儿期 T2WI 上(4 个 MR 图像,9-26 月龄)。在 2 岁及以上的儿童中,双侧苍白球高信号在 T2WI 上局限于边界(8 个 MR 图像,20 个月至 13 岁)。值得注意的是,有 2 例儿童在 2 个月龄时 MR 成像正常。因此,核黄疸病理的 MR 成像表现随时间演变,首先在 T1WI 上,随后在 T2WI 上显现,在婴儿早期存在“盲窗”期。T2WI 信号改变最初累及整个苍白球,随后局限于边界。除了 2 例患者外,之前的研究者均未诊断出核黄疸。
所有患者均具有特征性的临床表现和体征以及进行性的 MR 成像模式。然而,核黄疸的诊断常常被忽视。对后续 MR 图像的异常认识不足。