General Medicine, Buckinghamshire Healthcare NHS Trust, Buckinghamshire, UK.
Imperial College London School of Medicine, London, UK.
Br J Hosp Med (Lond). 2024 Aug 30;85(8):1-6. doi: 10.12968/hmed.2024.0236. Epub 2024 Aug 15.
A 21-year-old gentleman presented with low responsiveness and an unwitnessed tonic-clonic seizure. A 3-day history of fevers, headaches, and poor sleep was reported. He was initially treated for meningoencephalitis. Subsequently, he developed an erythematous rash over the face and chest. He had three generalised tonic-clonic seizures and his Glasgow Coma Score (GCS) deteriorated to 8 out of 15 requiring intubation and ventilation, and antiepileptics. Lumbar puncture (LP) results were unremarkable; however, the computed tomography (CT) head concluded bilateral haemorrhages and commented on the possibility of cerebral venous sinus thrombosis (CVST). Computed tomography venogram (CTV) confirmed CVST in the superior sagittal sinus, cortical vein and left transverse sinus. Repeat CT head revealed no new changes. Clinically, he exhibited residual left-sided weakness following stroke secondary to CVST. The patient was discharged with lifelong warfarin due to unprovoked CVST. He re-presented ten months later with persistent headaches. Clinical review noted bilateral papilloedema and he required LP to relieve raised intracranial pressure (ICP). In a 5-year follow-up, he continues to have raised ICP and associated headaches requiring further LPs. He continues to take warfarin, levetiracetam and topiramate, for headaches. This is an atypical case of CVST presenting initially with meningoencephalitis-like symptoms, demonstrating diverse clinical presentation. Ergo, this encourages an early multidisciplinary approach in presentations of headaches and seizures as clinical suspicion for CVST is high. Ultimately, this will appropriately identify patients for neuroimaging with computed tomography/magnetic resonance venogram. Furthermore, 5-year follow-up is presented in this case highlighting the importance of long-term follow-up in view of variable long-term complications that remain difficult to predict.
一位 21 岁的男士表现出反应迟钝和未经目击的强直阵挛性发作。据报告,他有 3 天的发热、头痛和睡眠不佳病史。他最初被诊断为脑膜炎脑炎。随后,他的面部和胸部出现红斑疹。他发生了 3 次全身性强直阵挛性发作,格拉斯哥昏迷评分(GCS)降至 15 分中的 8 分,需要插管和通气,并使用抗癫痫药物。腰椎穿刺(LP)结果无明显异常;然而,头部计算机断层扫描(CT)得出双侧出血的结论,并提到了脑静脉窦血栓形成(CVST)的可能性。计算机断层静脉造影(CTV)证实了上矢状窦、皮质静脉和左侧横窦的 CVST。头部 CT 复查未见新变化。临床检查显示,由于 CVST 继发的中风,他遗留左侧肢体无力。由于 CVST 引起的自发性 CVST,该患者出院后需终身服用华法林。10 个月后,他因持续性头痛再次就诊。临床检查发现双侧视乳头水肿,需要 LP 以缓解颅内压升高(ICP)。在 5 年的随访中,他的 ICP 持续升高,并伴有头痛,需要进一步 LP 治疗。他继续服用华法林、左乙拉西坦和托吡酯来治疗头痛。这是一例不典型 CVST 病例,最初表现为类似脑膜炎的症状,表现出不同的临床表现。因此,这鼓励在头痛和癫痫发作的表现中尽早采用多学科方法,因为 CVST 的临床怀疑很高。最终,这将适当地为患者进行神经影像学检查,包括计算机断层扫描/磁共振静脉造影。此外,在本病例中还进行了 5 年的随访,强调了在存在难以预测的各种长期并发症的情况下进行长期随访的重要性。