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华法林治疗相关的自发性胸段硬膜下血肿:病例报告及系列磁共振成像

Spontaneous thoracic subdural hematoma associated with warfarin therapy: Case report with serial MRI.

作者信息

Bunevicius Adomas, Tamasauskas Arimantas, Ambrozaitis Kazys Vytautas

机构信息

Department of Neurosurgery, Hospital of Lithuanian University of Health Sciences Kaunas Clinics, Kaunas, Lithuania.

Neuroscience Institute, Lithuanian University of Health Sciences, Kaunas, Lithuania.

出版信息

Surg Neurol Int. 2019 Mar 11;10:28. doi: 10.4103/sni.sni_384_17. eCollection 2019.

Abstract

BACKGROUND

Spontaneous acute spinal subdural hematoma (SASSDH) is a rare but serious condition. We present diagnostic challenges and serial magnetic resonance imaging (MRI) findings of a patient who developed warfarin-associated thoracic SASSDH that was managed surgically.

CASE DESCRIPTION

A 68-year-old male presented with sudden onset left-sided chest and back pain, left leg weakness, and bilateral loss of sensations below T4 level. His symptoms developed after strenuous physical activity. He was taking warfarin for atrial fibrillation. His admission international normalized ratio was 4.25. Deterioration of neurological status 3 days after admission prompted spinal computed tomography (CT) scan that demonstrated nonhomogenous hyperdense intradural mass lesion in the thoracic spine. MRI demonstrated heterogeneous mass lesion on the left side of the spinal canal and thoracic myelopathy. The patient underwent urgent surgical evacuation of subacute subdural hematoma extending from T3 to T6 levels. MRI scan following the surgery showed no signs of the hematoma and thoracic myelopathy. MRI at 3 months follow-up demonstrated myelopathy extending from T3 to T6 levels with deviation of the spinal cord. The patient's motor strength and sensations improved but he retained left leg weakness with sensory deficit below T8 level.

CONCLUSIONS

Spinal subdural hematoma should be suspected in patients presenting with acute onset back pain and myelopathy in the absence of trauma history. Coagulopathy should raise the suspicion for SASSDH. MRI is a valuable imaging modality for initial diagnosis to rule-out other lesions, and to assess postoperative re-bleeding and residual lesions.

摘要

背景

自发性急性脊髓硬膜下血肿(SASSDH)是一种罕见但严重的病症。我们报告了一名发生华法林相关胸椎SASSDH并接受手术治疗患者的诊断挑战及系列磁共振成像(MRI)表现。

病例描述

一名68岁男性,突发左侧胸背部疼痛、左腿无力,T4水平以下双侧感觉丧失。其症状在剧烈体力活动后出现。他因心房颤动正在服用华法林。入院时国际标准化比值为4.25。入院3天后神经功能状态恶化,促使进行脊柱计算机断层扫描(CT),显示胸椎硬膜内有不均匀高密度肿块病变。MRI显示椎管左侧有不均匀肿块病变及胸椎脊髓病。患者接受了从T3至T6水平的亚急性硬膜下血肿紧急手术清除。术后MRI扫描显示无血肿及胸椎脊髓病迹象。3个月随访时的MRI显示脊髓病从T3延伸至T6水平,脊髓有偏移。患者的运动力量和感觉有所改善,但仍遗留左腿无力及T8水平以下感觉缺失。

结论

对于无创伤史而出现急性背痛和脊髓病的患者,应怀疑有脊髓硬膜下血肿。凝血功能障碍应增加对SASSDH的怀疑。MRI是用于初步诊断以排除其他病变、评估术后再出血和残留病变的有价值的成像方式。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef9c/6499461/0b18d5e4c36a/SNI-10-28-g001.jpg

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