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首页> 外文期刊>Clinical neurology and neurosurgery >A case report of rapid spontaneous redistribution of acute supratentorial subdural hematoma to the entire spinal subdural space presenting as a Pourfour du Petit Syndrome and review of the literature
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A case report of rapid spontaneous redistribution of acute supratentorial subdural hematoma to the entire spinal subdural space presenting as a Pourfour du Petit Syndrome and review of the literature

机译:急性上上硬膜下硬膜下血肿快速自发性重新分布为整个脊柱硬膜下腔的病例报告,表现为Pourfour du Petit综合征,并复习文献

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Objective: This report illustrates the rare rapid spontaneous redistribution of an acute intracranial supratentorial subdural hematoma (AISSDH) to the entire spinal subdural space (SSS). The study is also unique in that the spinal subdural hematoma (SSH) manifested by the extremely rare Pourfour du Petit Syndrome (PPS). Methods: A 66-year-old man sustained blunt head trauma. On admission to the regional hospital, he scored 6 on GCS and his pupils were of equal size reacting to light. Initial computed tomography (CT) scan showed a unilateral AISSDH. The patient was referred to our department and arrived 16 h following the accident, at which time a repeat CT scan revealed almost complete resolution of the AISSDH without clinical improvement. On the 9th postinjury day transient anisocoria and tachycardia without spinal symptomatology developed. Since neither neurological examination nor follow-up CT scans showed intracranial pathology explaining the anisocoria, the patient was treated further conservatively. During the next 3 days circulatory instability developed and the patient succumbed to primary traumatic injury. Autopsy revealed a SSH occupying the entire SSS. Conclusion: This case calls attention to the unique combination of the displacement of an AISSDH to the SSS and the presentation of this clinical entity by the PPS.
机译:目的:本报告说明了急性颅内上硬膜下硬膜下血肿(AISSDH)在整个脊髓硬膜下间隙(SSS)中罕见的快速自发性再分布。该研究的独特之处还在于脊柱硬膜下血肿(SSH)表现为极为罕见的Pourfour du Petit综合征(PPS)。方法:一名66岁的男子头部受到钝性创伤。进入地区医院后,他在GCS上得分为6,他的学生对光的反应大小相同。最初的计算机体层摄影(CT)扫描显示单侧AISSDH。该患者被转介到我们的部门,并在事故发生后16小时到达,此时再次进行CT扫描发现AISSDH几乎完全消失,而没有临床改善。受伤后第9天出现无脊髓症状的短暂性房间隔和心动过速。由于神经系统检查和后续CT扫描均未显示颅内病变可解释该异房症,因此对该患者进行了进一步的保守治疗。在接下来的三天中,循环系统变得不稳定,患者屈服于原发性创伤。验尸显示,SSH占用了整个SSS。结论:该病例引起人们对AISSDH置换为SSS的独特结合以及PPS对该临床实体的展示的独特结合。

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