Acute hemiparesis ================= * Da-Wei Huang * Jui-Ming Sun * Yu-Hao Chen * Kuo-Chang Huang ## A rare presentation of spontaneous spinal epidural hematoma mimicking acute stroke ## Abstract Acute hemiparesis is an extremely rare presentation of spontaneous spinal epidural hematoma, which may be misdiagnosed as acute ischemic stroke and improperly treated with an intravenous thrombolytic agent. Here, we report a case of a 54-year-old woman who presented with acute neck pain and right-sided weakness. She was initially suspected of having ischemic stroke and therefore treated with an intravenous thrombolytic agent. However, she developed progressive tetraparesis, and subsequent magnetic resonance images confirmed cervical spontaneous spinal epidural hematoma. Stroke is a leading cause of mortality and morbidity in Taiwan.1 Acute hemiparesis is one of the most indicative manifestations of acute stroke. Administration of recombinant tissue plasminogen activator (rtPA), a thrombolytic agent, within 3 to 4.5 hours of symptom onset is the standard treatment for acute ischemic stroke.2 However, various diseases such as slipped cervical discs, epilepsy, and spinal epidural hematoma may present along with acute hemiparesis, mimicking acute stroke, and thus be inappropriately treated with rtPA.3 Spontaneous spinal epidural hematoma (SSEH) is a rare condition of unknown etiology and requires urgent surgical intervention.3-5 The characteristic manifestation of SSEH is sudden-onset neck pain following by motor paralysis or tetraparesis.4 However, SSEH presenting with acute hemiparesis has been rarely reported in the literature. Therefore, we reported a case of SSEH with acute hemiparesis wrongly treated with rtPA in the emergency department (ED). ## Case Report ### Patient information The informed consent was obtained from the patient for the case report. The timeline for this case report was summarized in **Table 1**. A 54-year-old woman experienced sudden-onset neck pain, right facial numbness, and right-sided weakness. After these symptoms had persisted for 2 hours, she visited our ED. She denied a history of hypertension, taking anticoagulant/antiplatelet medication, or trauma events. View this table: [TABLE 1](http://nsj.org.sa/content/25/4/316/T1) TABLE 1 The timeline for the presented case. ### Clinical findings On arrival, she was alert and cognizant. Her vital signs were as follows: blood pressure of 113/73 mm Hg (normal range: 90/60mmHg to 120/80mmHg), heart rate of 74 beats per minute (normal range: 60 to 100 beats per minute), respiratory rate of 20 breaths per minute (normal range: 12 to 16 breaths per minute), and body temperature of 36.1°C (normal range: 36.1 to 37.2). Neurological examination revealed Grade 2 (of 5) muscle power in the right extremities, normal deep tendon reflexes, and a right Babinski sign. Cranial nerve function was normal, except for decreased sensation on the right side of the face. Laboratory examination revealed a hemoglobin level of 10.8 mg/dL (normal range: 12-15.5mg/dl) and platelet count of 263,000/μL (normal range: 150,000 to 450,000/uL). A coagulation test produced normal results. An emergency computed tomography (CT) scan of the brain revealed no intracranial hemorrhage. CT angiography revealed no evidence of major vessel occlusion or artery dissection. Her National institutes of health stroke scale was 11 (normal range: 0 to 42). As acute ischemic stroke is highly suspected with right hemiparesis, intravenous rtPA was administrated within 4.5 hours of symptom onset. ### Diagnostic assessment However, the right side progressively weakened after rtPA administration, and left-side weakness developed 3 hours later. The patient remained alert and oriented. Grade 2 (of 5) muscle power was found in the left extremities. Subsequent magnetic resonance (MR) images of the brain and cervical spine revealed a mass in the right dorsal portion of the cervical canal above the C3 level that was compressing the spinal cord (**Figure 1A**). The mass was isointense on T1-weighted images (**Figure 1B**) and hyperintense on T2-weighted images (**Figure 1C**). ![Figure 1](http://nsj.org.sa/https://nsj.org.sa/content/nsj/25/4/316/F1.medium.gif) [Figure 1](http://nsj.org.sa/content/25/4/316/F1) Figure 1 Magnetic resonance images of the cervical spine showing **A**) Axial T2-weighted image shows a mass (white arrow) in the right dorsal portion of the cervical canal above the C3 level, compressing the spinal cord. **B**) Sagittal T1-weighted image shows mass isointensity (white arrow). **C**) Sagittal T2-weighted image shows high mass intensity (white arrow). ### Therapeutic intervention With a diagnosis of cervical SSEH, the patient underwent emergent laminectomy with hematoma removal 12 hours after symptom onset. The hematoma was located primarily on the dorsal aspect of the right spinal canal above the C3 level and was severely compressing the spinal cord (**Figure 2**). Pathological examination confirmed the diagnosis of hematoma without vascular abnormality. The intraoperative blood loss was 50 mL. ![Figure 2](http://nsj.org.sa/https://nsj.org.sa/content/nsj/25/4/316/F2.medium.gif) [Figure 2](http://nsj.org.sa/content/25/4/316/F2) Figure 2 Intraoperative view following laminectomy; hematoma (white arrow) mainly located on the right dorsal aspect of the C3 region. ### Follow-up and outcomes Postoperatively, her neurological deficits decreased gradually. On the fifth postoperative day, the motor strength of the left extremities recovered to grade 4. The motor strength of the right extremities recovered to grade 3 at discharge. She could walk with the walker one month after the surgery. ## Discussion Spontaneous spinal epidural hematoma is a rare etiology of acute hemiparesis that can cause spinal cord compression. The annual incidence of SSEH is approximately 0.1 per 100,000, and most cases are observed in men aged between 50 and 80 years.4 Spontaneous spinal epidural hematoma is caused by many factors, such as hypertension, coagulopathy, anticoagulant/antiplatelet therapy, neoplasm, hemodialysis, vascular abnormality, and idiopathic causes.3,5 Although the pathophysiological mechanism is unclear, bleeding in SSEH has been hypothesized to be associated with activities resulting in a sudden increase in posterior epidural venous pressure, such as cough, sneezing, twisting, lifting, and straining.3-6 Patients with cervical SSEH commonly present with sudden-onset neck pain and subsequent rapid motor paralysis or sensory dysfunction.7 However, acute hemiparesis has been reported to be an extremely rare presentation of SSEH.5,8,9 Such cases may be initially misdiagnosed as acute ischemic stroke, which commonly presents with acute hemiparesis and is treated with intravenous thrombolytic agents in the ED.5,8,10 Kim et al3 showed that 2 (22.2%) of 9 patients initially misdiagnosed with ischemic stroke and treated with intravenous rtPA actually had SSEH. Clinical manifestations such as Horner syndrome, Brown-Sequard syndrome, and the absence of cranial nerve palsies in acute hemiparesis indicate SSEH rather than stroke; after observing such manifestations, Patel et al9 showed that 13 patients suspected of having stroke and treated with heparin, rtPA, or warfarin actually had SSEH. Furthermore, Matsumoto et al8 concluded that initial symptoms of neck pain and the Lhermitte sign are the most crucial for distinguishing SSEH from acute ischemic stroke. The soft tissue window of a CT scan may enable physicians to rule out cerebrovascular or cardiovascular disease and identify SSEH.11 Magnetic resonance imaging is the standard method for diagnosing SSEH and can help determine the location, contours, and severity of cord compression.4 In the acute stage, hematoma commonly appears as an isosignal on T1-weighted MR images and a high signal on T2-weighted MR images.4,7 Enhanced MR imaging or MR angiography may be helpful in differentiating SSEH from other disorders presenting with hemiparesis, including ischemic stroke, prolapsed cervical discs, epidural abscesses, neoplasms, or transverse myelitis.9 Although few cases (mainly from pediatric patients) with spontaneous resolution following conservative treatment have been described,12-14 decompressive laminectomy with hematoma evacuation is the standard care procedure for patients with SSEH presenting with neurological deficitis.4,9,11 The outcome is correlated with the delay from symptom onset until surgical intervention.9 Surgical decompression after more than 12 hours of profound deficits may cause permanent neurological disability.15 However, the effects of rtPA on the surgical outcome and intraoperative bleeding tendency are unclear because few SSEH patients are treated with intravenous rtPA.10 In our case, the operation was performed 8 hours after intravenous rtPA treatment, and the intraoperative blood loss was only 50 mL. Thus, the effect of one-time intravenous rtPA administration on surgical intervention is negligible. In patient’s perspective, cervical SSEH must be considered when sudden onset of neck pain following by motor weakness occurs, without obvious cranial nerve abnormalities such as facial palsy or tongue deviation. In conclusion, although acute hemiparesis is the main presentation of acute stroke in the ED, cervical SSEH must be considered when a patient presents with neck pain but no obvious cranial nerve abnormalities, such as facial palsy or tongue deviation. Improper use of rtPA may cause cervical SSEH to progress, delay surgical intervention, and worsen the surgical outcome. ## Acknowledgements *We would like to thank Dr. Cheng-Ta Hsieh (Sijhih Cathay General Hospital, New Taipei, Taiwan) for providing assistance in the preparation of the manuscript.* ## Footnotes * **Disclosure.** The all authors certify that they have NO affiliations with or involvement in any organization or entity with any financial interest (such as honoraria; educational grants; participation in speakers’ bureaus; membership, employment, consultancies, stock ownership, or other equity interest; and expert testimony or patent-licensing arrangements), or non-financial interest (such as personal or professional relationships, affiliations, knowledge or beliefs) in the subject matter or materials discussed in this manuscript. * Received March 2, 2020. * Accepted June 14, 2020. * Copyright: © Neurosciences Neurosciences is an Open Access journal and articles published are distributed under the terms of the Creative Commons Attribution-NonCommercial License (CC BY-NC). 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