Internal Medicine, Medical College and Hospital Kolkata, Kolkata, West Bengal, India.
Internal Medicine, RG Kar Medical College and Hospital, Kolkata, West Bengal, India
BMJ Case Rep. 2021 Oct 19;14(10):e246073. doi: 10.1136/bcr-2021-246073.
Inherited thrombophilic disorders are well-established predisposing factors for venous thromboembolism, but their role in arterial ischaemic stroke is uncertain. The exact mechanism of arterial thrombosis in thrombophilias remains elusive. Herein, we report a case of a 30-year-old woman who was admitted to our facility with sudden-onset right-sided ptosis and ophthalmoplegia. Detailed clinical features, neuroimaging and laboratory evaluation clinched the diagnosis of ischaemic stroke in midbrain due to microvascular obstruction associated with isolated protein S deficiency. She was treated with oral anticoagulant (warfarin) and physiotherapy; without any improvement of her symptoms at 2 months of follow-up. A high index of clinical suspicion is needed in any case of young ischaemic stroke in absence of common cardiac and vascular risk factors, to recognise the presence of inherited thrombophilia.
遗传性血栓形成倾向是静脉血栓栓塞的既定易患因素,但它们在动脉缺血性卒中中的作用尚不确定。血栓形成倾向中动脉血栓形成的确切机制仍难以捉摸。在此,我们报告了一例 30 岁女性,因突发右侧上睑下垂和眼肌麻痹而入住我院。详细的临床特征、神经影像学和实验室评估确定了由于孤立性蛋白 S 缺乏症引起的微血管阻塞导致中脑缺血性卒中的诊断。她接受了口服抗凝剂(华法林)和物理治疗;在 2 个月的随访中,她的症状没有任何改善。在无常见心脏和血管危险因素的情况下,任何年轻的缺血性卒中病例都需要高度的临床怀疑,以识别遗传性血栓形成倾向的存在。