Levee Viva, Sivaganesh Karthikeyan, Schaeffer Andrew, Karunaratne Kushan
Imperial College Healthcare NHS Trust, London, UK.
Imperial College London, London, UK.
Pract Neurol. 2025 Jan 16;25(1):56-59. doi: 10.1136/pn-2024-004232.
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.
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。