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发热伴睾丸炎患者接受利妥昔单抗治疗后发生致命性蜱传脑炎(鹿蜱病毒,谱系 II)

Fatal Powassan Encephalitis (Deer Tick Virus, Lineage II) in a Patient With Fever and Orchitis Receiving Rituximab.

机构信息

Neuropathology Division, Department of Pathology, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts.

Department of Neurology, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts.

出版信息

JAMA Neurol. 2018 Jun 1;75(6):746-750. doi: 10.1001/jamaneurol.2018.0132.

Abstract

IMPORTANCE

Powassan virus is a rare but increasingly recognized cause of severe neurological disease.

OBJECTIVE

To highlight the diagnostic challenges and neuropathological findings in a fatal case of Powassan encephalitis caused by deer tick virus (lineage II) in a patient with follicular lymphoma receiving rituximab, with nonspecific anti-GAD65 antibodies, who was initially seen with fever and orchiepididymitis.

DESIGN, SETTING, AND PARTICIPANTS: Comparison of clinical, radiological, histological, and laboratory findings, including immunohistochemistry, real-time polymerase chain reaction, antibody detection, and unbiased sequencing assays, in a single case report (first seen in December 2016) at an academic medical center.

EXPOSURE

Infection with Powassan virus.

MAIN OUTCOMES AND MEASURES

Results of individual assays compared retrospectively.

RESULTS

In a 63-year-old man with fatal Powassan encephalitis, serum and cerebrospinal fluid IgM antibodies were not detected via standard methods, likely because of rituximab exposure. Neuropathological findings were extensive, including diffuse leptomeningeal and parenchymal lymphohistiocytic infiltration, microglial proliferation, marked neuronal loss, and white matter microinfarctions most severely involving the cerebellum, thalamus, and basal ganglia. Diagnosis was made after death by 3 independent methods, including demonstration of Powassan virus antigen in brain biopsy and autopsy tissue, detection of viral RNA in serum and cerebrospinal fluid by targeted real-time polymerase chain reaction, and detection of viral RNA in cerebrospinal fluid by unbiased sequencing. Extensive testing for other etiologies yielded negative results, including mumps virus owing to prodromal orchiepididymitis. Low-titer anti-GAD65 antibodies identified in serum, suggestive of limbic encephalitis, were not detected in cerebrospinal fluid.

CONCLUSIONS AND RELEVANCE

Owing to the rarity of Powassan encephalitis, a high degree of suspicion is required to make the diagnosis, particularly in an immunocompromised patient, in whom antibody-based assays may be falsely negative. Unbiased sequencing assays have the potential to detect uncommon infectious agents and may prove useful in similar scenarios.

摘要

重要性

波瓦桑病毒是一种罕见但日益被认识到的严重神经疾病病因。

目的

强调在一例滤泡性淋巴瘤患者中,由于鹿蜱病毒(谱系 II)引起的致命波瓦桑脑炎的诊断挑战和神经病理学发现。该患者正在接受利妥昔单抗治疗,伴有非特异性抗 GAD65 抗体,最初表现为发热和附睾炎。

设计、设置和参与者:在一家学术医疗中心的单一病例报告(首次于 2016 年 12 月就诊)中,对临床、影像学、组织学和实验室发现进行比较,包括免疫组织化学、实时聚合酶链反应、抗体检测和无偏测序检测。

暴露

感染波瓦桑病毒。

主要结果和措施

回顾性比较各个检测结果。

结果

在一例 63 岁患有致命性波瓦桑脑炎的男性中,血清和脑脊液中的 IgM 抗体通过标准方法未被检测到,这可能是由于利妥昔单抗暴露所致。神经病理学发现广泛,包括弥漫性软脑膜和实质淋巴组织细胞浸润、小胶质细胞增生、明显的神经元丢失以及白质微梗死,小脑、丘脑和基底节最严重。通过 3 种独立的方法在死后做出诊断,包括在脑活检和尸检组织中检测到波瓦桑病毒抗原、通过靶向实时聚合酶链反应在血清和脑脊液中检测到病毒 RNA,以及通过无偏测序在脑脊液中检测到病毒 RNA。广泛的其他病因检测结果均为阴性,包括由于附睾炎前驱症状而排除的腮腺炎病毒。血清中检测到低滴度的抗 GAD65 抗体,提示边缘性脑炎,但未在脑脊液中检测到。

结论和相关性

由于波瓦桑脑炎罕见,因此需要高度怀疑才能做出诊断,特别是在免疫功能低下的患者中,抗体检测可能会出现假阴性。无偏测序检测有可能检测到不常见的病原体,并且在类似情况下可能会很有用。

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