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急性出血性白质脑炎:法医病理学家需识别的关键病症。

Acute hemorrhagic leukoencephalitis: a critical entity for forensic pathologists to recognize.

作者信息

Lann Meredith A, Lovell Mark A, Kleinschmidt-DeMasters B K

机构信息

Department of Pathology, University of Colorado Denver, Aurora, Colo., USA.

出版信息

Am J Forensic Med Pathol. 2010 Mar;31(1):7-11. doi: 10.1097/PAF.0b013e3181c6be92.

Abstract

Acute hemorrhagic leukoencephalopathy (AHLE) is a rare, acute disorder characterized by perivenular demyelination and diffuse hemorrhagic necrosis of the central nervous system. AHLE is thought to represent a hyperacute form of acute disseminated encephalomyelitis. AHLE is associated with a greater morbidity and mortality and, fortunately, is much less common than acute disseminated encephalomyelitis. Since most cases of AHLE result in patient demise, forensic pathologists should be cognizant of this entity and consider it in their differential diagnosis.Here we describe an interesting case of a previously healthy 11-year-old boy who initially complained of vague gastroenteritis-like symptoms while visiting a mountain lake. The boy's symptoms evolved to include severe headache and dizziness, necessitating a visit to a rural emergency department. He presented with focal neurologic findings, and head computed tomography (CT) scan confirmed thalamic edema. Cerebrospinal fluid analysis was suggestive of infectious etiology, and multiple empiric therapies were initiated. He was transferred to our institution, and his clinical status continued to worsen. Given the poor prognosis, the family requested withdrawal of supportive care. On day 14 of symptoms the boy succumbed to his illness. An autopsy was requested to further characterize the proximate cause of death.AHLE often presents with abrupt onset of fever, neck stiffness, seizure, and/or focal neurologic signs several days following a viral illness or vaccination. Thus, AHLE can clinically mimic a direct central nervous system infection or a toxic ingestion. AHLE has a very poor prognosis, with rapid deterioration and death usually occurring within days to one week after onset of symptoms. The cause for AHLE is unclear. An autoimmune pathophysiology is likely, with immune cross-reactivity between myelin basic protein moieties and various infectious agent antigens. Treatment for AHLE is not well-established; some authors describe in recent literature that a combination of immunosuppressant medications and/or therapeutic plasma exchange may be of benefit in treating AHLE.

摘要

急性出血性白质脑病(AHLE)是一种罕见的急性疾病,其特征为中枢神经系统的血管周围脱髓鞘和弥漫性出血性坏死。AHLE被认为是急性播散性脑脊髓炎的超急性形式。AHLE的发病率和死亡率更高,幸运的是,它比急性播散性脑脊髓炎少见得多。由于大多数AHLE病例会导致患者死亡,法医病理学家应认识到这一实体,并在鉴别诊断中加以考虑。在此,我们描述了一例有趣的病例,一名先前健康的11岁男孩,他在游览山间湖泊时最初抱怨有类似肠胃炎的模糊症状。男孩的症状逐渐发展为包括严重头痛和头晕,因此需要前往农村急诊科就诊。他出现了局灶性神经学表现,头部计算机断层扫描(CT)证实丘脑水肿。脑脊液分析提示感染性病因,并开始了多种经验性治疗。他被转到我们机构,其临床状况持续恶化。鉴于预后不佳,家属要求停止支持治疗。在出现症状的第14天,男孩因病死亡。家属要求进行尸检以进一步明确死亡的直接原因。AHLE通常在病毒感染或接种疫苗几天后突然出现发热、颈部僵硬、癫痫发作和/或局灶性神经体征。因此,AHLE在临床上可能类似于直接的中枢神经系统感染或中毒性摄入。AHLE的预后非常差,通常在症状出现后的几天到一周内迅速恶化并死亡。AHLE的病因尚不清楚。可能存在自身免疫病理生理机制,髓磷脂碱性蛋白部分与各种感染原抗原之间存在免疫交叉反应。AHLE的治疗方法尚未完全确立;一些作者在最近的文献中描述,免疫抑制药物和/或治疗性血浆置换联合使用可能对治疗AHLE有益。

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