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成年期神经退行性变的儿童静态脑病(SENDA)患者的磁共振成像(MRI)、磁共振波谱成像(MR spectroscopy)及弥散张量成像(diffusion tensor imaging)结果

MRI, MR spectroscopy, and diffusion tensor imaging findings in patient with static encephalopathy of childhood with neurodegeneration in adulthood (SENDA).

作者信息

Kimura Yukio, Sato Noriko, Sugai Kenji, Maruyama Shinsuke, Ota Miho, Kamiya Kouhei, Ito Kimiteru, Nakata Yasuhiro, Sasaki Masayuki, Sugimoto Hideharu

机构信息

Department of Radiology, National Center of Neurology and Psychiatry, Kodaira, Tokyo, Japan.

出版信息

Brain Dev. 2013 May;35(5):458-61. doi: 10.1016/j.braindev.2012.07.008. Epub 2012 Aug 11.

Abstract

Static encephalopathy of childhood with neurodegeneration in adulthood (SENDA) is a recently established disorder that is a subtype of neurodegeneration with brain iron accumulation (NBIA). We presented the first case report of SENDA of a 39-year-old female. She had psychomotor retardation from childhood and remained static for two decades. Then, at the age of 30, she developed severe dystonia and parkinsonism. Brain MRI revealed T2-weighted hypointensity signal in the globus pallidus and substantia nigra, and T1-weighted hyperintensity signal in the substantia nigra with a central hypointensity area. These clinical and imaging findings are characteristic of SENDA. Advanced MRI, including (1)H-MR spectroscopy (MRS) and diffusion tensor imaging (DTI), demonstrated similar findings of pantothenate kinase-associated neurodegeneration (PKAN), which is a major syndrome of SENDA. MRI plays a crucial role in the diagnosis of NBIA, especially SENDA.

摘要

儿童期静态性脑病伴成年期神经退行性变(SENDA)是一种最近确定的疾病,是脑铁沉积神经退行性变(NBIA)的一种亚型。我们报告了首例39岁女性SENDA病例。她自幼出现精神运动发育迟缓,病程停滞20年。随后,在30岁时,她出现了严重的肌张力障碍和帕金森综合征。脑部MRI显示苍白球和黑质T2加权低信号,黑质T1加权高信号且中央有低信号区。这些临床和影像学表现是SENDA的特征。先进的MRI,包括氢质子磁共振波谱(MRS)和弥散张量成像(DTI),显示出与泛酸激酶相关神经退行性变(PKAN)相似的表现,PKAN是SENDA的主要综合征。MRI在NBIA尤其是SENDA的诊断中起着关键作用。

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