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首页> 外文期刊>American Journal of Case Reports >Clinically Isolated Brainstem Progressive Multifocal Leukoencephalopathy: Diagnostic Challenges
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Clinically Isolated Brainstem Progressive Multifocal Leukoencephalopathy: Diagnostic Challenges

机译:临床上孤立的脑干渐进式多焦白血病:诊断挑战

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Patient: Female, 47-year-old Final Diagnosis: Brainstem progressive multifocal leukoencephalopathy Symptoms: Dizziness ? intermittent slurred speech ? right-sided facial droop and numbness Medication: — Clinical Procedure: Lumbar puncture Specialty: Neurology Objective: Mistake in diagnosis Background: Acute brainstem syndrome (ABS), as the initial manifestation of progressive multifocal leukoencephalopathy (PML), is rarely reported. Appropriate history and neurodiagnostic testing are essential to encompass the extended spectrum of clinical and radiological differentials of ABS. Case Report: A 47-year-old woman presented to the emergency department with slurred speech, dizziness, right-sided facial droop, and numbness. Brain magnetic resonance imaging (MRI) revealed non-enhancing hyperintensities in the right lateral pons and brachium pontis, eventually extending to the bilateral middle cerebellar peduncle, pons, left&right cerebellar hemisphere, right thalamocapsular region, and midbrain region. Lumbar puncture revealed 3 cerebrospinal fluid-specific oligoclonal bands. Initial diagnosis of multiple sclerosis led to high-dose intravenous steroid treatment. The patient continued to deteriorate, leading to multiple emergency department visits and hospital admissions. Additional history revealing previously diagnosed, treatment-naive HIV prompted a repeat lumbar puncture. Cerebrospinal fluid polymerase chain reaction (PCR) for JC polyomavirus (JCV) was positive, leading to the diagnosis of clinically isolated brainstem PML. Unfortunately, the patient developed pneumonia and hypoxic respiratory failure, which ultimately led to her death. Conclusions: This case highlights the need for considering isolated brainstem PML, as a diagnostic possibility, in patients presenting with acute-subacute brainstem symptoms and compatible neuroimaging findings. Clinicians need to be aware of varying PML presentations with brainstem or diencephalic variants, as well as monofocal lesions. The prognosis for PML has improved somewhat, secondary to immune reconstitution by highly active antiretroviral therapy, risk stratification in drug-induced PML, and other emerging treatments, such as pembrolizumab.
机译:病人:女性,47岁的最终诊断:脑干进步多焦点白血病症状:头晕?间歇性浆料?右侧的面部下垂和麻木药物: - 临床手术:腰椎穿刺专业:神经病学目标:诊断背景:急性脑干综合征(ABS),作为渐进式多焦白血病(PML)的初始表现,很少报道。适当的历史和神经发电虫测试对于包含ABS的临床和放射性差异的扩展谱是必不可少的。案例报告:一名47岁的女性向急诊部门提交,言语,头晕,右侧面部下垂和麻木。脑磁共振成像(MRI)揭示了在右侧PON和BONTIS中的不增强的超萎缩性,最终延伸到双侧中部小脑花序梗,PON,左& GT;右小脑半球,右丘脑区域和中脑区域。腰椎穿刺显示出3个脑脊液特异性的寡胶带。初步诊断多发性硬化导致高剂量静脉类固醇治疗。患者继续恶化,导致多次急诊部门访问和医院入学。额外的历史揭示先前诊断出的治疗,幼稚的艾滋病毒促使重复腰椎穿刺。 JC PolyomaVirus(JCV)的脑脊液聚合酶链式反应(PCR)是阳性的,导致临床孤立的脑干PML的诊断。不幸的是,患者发育了肺炎和缺氧呼吸衰竭,最终导致了她的死亡。结论:这种情况强调了在患有急性亚急性脑干症状和相容的神经影像体验的患者中考虑分离的脑干PML作为诊断可能性的需求。临床医生需要意识到具有脑干或Diencephalic变体的PML演示,以及单焦病变。通过高度活跃的抗逆转录病毒治疗,药物诱导的PML的风险分层和其他新出现的治疗,例如Pembrolizumab等新出现治疗,其预后已经有所改善,继发于免疫重建,患有药物诱导的PML的风险分层。

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