Tsalouchidou Panagiota-Eleni, Juenemann Clara, Hahn Wiebke, Zahnert Felix, Möller Leona, Hakel Lukas, Kemmling André, Menzler Katja, Simon Ole J, Timmermann Lars, Knake Susanne, Bernhard Felix
Department of Neurology, University Hospital Gießen and Marburg, Marburg, Germany.
Epilepsy Center Hessen, Department of Neurology, Philipps University Marburg, Marburg, Germany.
Epilepsy Behav Rep. 2024 Oct 6;28:100716. doi: 10.1016/j.ebr.2024.100716. eCollection 2024.
This case series describes the clinical features, diagnostic challenges, treatment approaches, and outcomes of three adult patients with COQ8A-related CoQ10 deficiency presenting with focal status epilepticus, who were effectively treated at the Department of Neurology, Philipps University Marburg, Marburg, Germany. The patients, all from consanguineous families with the first two being siblings, presented with a late onset of the disease, characterized by progressive cerebellar ataxia and epilepsy, with clinical deterioration and focal status epilepticus occurring in adulthood. The first patient exhibited myoclonic status, while the second and third patients presented with bilateral tonic-clonic seizures followed by focal status epilepticus manifesting with cortical blindness. Despite differing semiologies, all patients displayed similar EEG findings with continuous or nearly continuous occipital sharp waves and spikes. MRI findings revealed focal changes in the Diffusion-Weighted Imaging (DWI) and Fluid Attenuated Inversion Recovery (FLAIR) sequences. Significant clinical improvement was observed following treatment with high doses of CoQ10, with the diffusion restriction abnormalities being reversible after therapy. In conclusion, consistent with existing literature, we observed a characteristic EEG pattern that can help identify the disease and facilitate early diagnosis and treatment. The diffusion restriction abnormalities on MRI were reversible after therapy, and high doses of CoQ10 proved beneficial even in cases of status epilepticus.
本病例系列描述了三名患有COQ8A相关辅酶Q10缺乏症且表现为局灶性癫痫持续状态的成年患者的临床特征、诊断挑战、治疗方法及预后,这三名患者在德国马尔堡菲利普斯大学神经内科得到了有效治疗。这些患者均来自近亲家庭,前两名是兄弟姐妹,疾病起病较晚,以进行性小脑共济失调和癫痫为特征,在成年期出现临床病情恶化和局灶性癫痫持续状态。第一名患者表现为肌阵挛状态,而第二名和第三名患者出现双侧强直阵挛发作,随后出现以皮质盲为表现的局灶性癫痫持续状态。尽管症状学不同,但所有患者脑电图表现相似,均有持续或近乎持续的枕部尖波和棘波。磁共振成像(MRI)结果显示弥散加权成像(DWI)和液体衰减反转恢复序列(FLAIR)有局灶性改变。高剂量辅酶Q10治疗后观察到显著的临床改善,治疗后弥散受限异常可逆转。总之,与现有文献一致,我们观察到一种特征性脑电图模式,有助于识别该疾病并促进早期诊断和治疗。MRI上的弥散受限异常在治疗后可逆转,高剂量辅酶Q10即使在癫痫持续状态的病例中也被证明是有益的。