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首页> 外文期刊>The Journal of pediatrics >Vigabatrin-Relatecl Magnetic Resonance imaging Abnormalities in an Infant with Tuberous Sclerosis Complex and Infantile Spasms
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Vigabatrin-Relatecl Magnetic Resonance imaging Abnormalities in an Infant with Tuberous Sclerosis Complex and Infantile Spasms

机译:伴结节性硬化症和小儿痉挛的婴儿的Vigabatrin-Relatecl磁共振成像异常

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摘要

Anewborn with hypopigmented skin macules, cardiac rhabdomyomas, and cerebral magnetic resonance imaging (MRI) demonstrating cortical tubers and sube-pendymal nodules (Figure, A) was diagnosed with tuberous sclerosis complex (TSC). Clusters of flexor spasms began at 3 months of age, infantile spasms was diagnosed. Treatment was commenced with vigabatrin, an irreversible inhibitor of y-aminobutyric acid transaminase, and the spasms ceased within 1 week. Routine follow-up MRI demonstrated the interval development of asymptomatic abnormalities, including restricted diffusion in the bilateral brainstem, basal ganglia, and thalami (Figure, B). After 1 year of successful treatment, the vigabatrin was discontinued and follow-up MRI demonstrated full resolution of these abnormalities (Figure, C).
机译:新生的色素沉着不足的皮肤黄斑,心脏横纹肌瘤和脑磁共振成像(MRI)表现出皮质块茎和皮下腺结节(图A),被诊断出患有结节性硬化症(TSC)。屈肌痉挛开始于3个月大,诊断为婴儿痉挛。用维加巴特林(一种不可逆的γ-氨基丁酸转氨酶抑制剂)开始治疗,痉挛在1周内停止。常规随访MRI显示无症状异常的间隔发展,包括双侧脑干,基底神经节和丘脑的扩散受限(图B)。在成功治疗1年后,停用了vigabatrin,并且随访MRI证实了这些异常的完全解决(图C)。

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