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POLG癫痫在孕期表现为新发难治性癫痫持续状态(NORSE)。

POLG epilepsy presenting as new-onset refractory status epilepticus (NORSE) in pregnancy.

作者信息

Levee Viva, Sivaganesh Karthikeyan, Schaeffer Andrew, Karunaratne Kushan

机构信息

Imperial College Healthcare NHS Trust, London, UK.

Imperial College London, London, UK.

出版信息

Pract Neurol. 2025 Jan 16;25(1):56-59. doi: 10.1136/pn-2024-004232.

Abstract

A 21-year-old woman developed explosive new-onset refractory status epilepticus when 18 weeks pregnant. She had been previously well with no history of seizures and a normal developmental history. She had initially presented with focal impaired awareness seizures but subsequently developed status epilepticus requiring intensive care unit admission and was successfully treated with multiple anti-seizure medications. Once stabilised she was stepped down to the inpatient neurology ward and then transferred to the tertiary centre for a planned late termination of pregnancy, which was the patient's choice. Following transfer, she again developed refractory status epilepticus, requiring intensive care readmission. Subsequent investigations identified a compound heterozygous POLG genetic mutation. We discuss the challenges in the acute clinical situation and important considerations in the diagnosis and management of POLG-related epilepsy.

摘要

一名21岁女性在怀孕18周时出现爆发性新发难治性癫痫持续状态。她此前身体健康,无癫痫病史,发育史正常。她最初表现为局灶性意识障碍性癫痫发作,但随后发展为癫痫持续状态,需要入住重症监护病房,并通过多种抗癫痫药物成功治疗。病情稳定后,她被转至神经内科住院病房,然后转至三级医疗中心,进行计划中的晚期妊娠终止,这是患者的选择。转院后,她再次出现难治性癫痫持续状态,需要再次入住重症监护病房。后续检查发现了复合杂合性POLG基因突变。我们讨论了急性临床情况下的挑战以及与POLG相关癫痫诊断和管理中的重要注意事项。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10c1/11877079/cf4798481462/pn-25-1-g001.jpg

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