Burden Zachary, Fasen Madeline, Judkins Benjamin L, Isache Carmen
Department of Medicine, University of Florida College of Medicine-Jacksonville, Florida, United States.
University of Florida College of Medicine-Gainesville, Florida, United States.
IDCases. 2019 Feb 13;15:e00505. doi: 10.1016/j.idcr.2019.e00505. eCollection 2019.
We present here a case of West Nile Virus (WNV) encephalitis that initially presented with diabetic ketoacidosis and rhabdomyolysis.
A 35-year-old male with no past medical history presented to the emergency department complaining of polydipsia, generalized weakness, lightheadedness, and visual disturbances of one week duration. He was found to be in diabetic ketoacidosis. His hemoglobin A1c was 11%. The patient was appropriately treated for diabetic ketoacidosis and it resolved on hospital day 1. On hospital day 2, the patient developed a fever of 101.6 °F and his mental status became severely altered. He developed auditory and visual hallucinations. IgM and IgG antibodies to West Nile Virus were positive in the cerebral spinal fluid (CSF). The patient's creatine kinase level rose to 118,400 U/L during his hospitalization and eventually returned to baseline. The patient made a full recovery with no residual neurologic deficits after an 11 day hospital course.
In this patient, neuroinvasive WNV was confirmed with positive CSF IgM. The patient's newly diagnosed diabetes likely contributed to his susceptibility to neuroinvasive disease. Furthermore, WNV encephalitis in a background of DKA has not been previously described in the literature and this case demonstrates WNV neuroinvasive disease should be in the differential diagnosis for patients presenting with unexplained neurological symptoms.
Diagnosis of neuroinvasive WNV is imperative to stop unnecessary therapies, limit further diagnostic evaluation, help predict patient outcomes, direct public health prevention measures, and further provide investigations into the clinical conditions that define the spectrum of WNV disease.
我们在此报告一例西尼罗河病毒(WNV)脑炎病例,该病例最初表现为糖尿病酮症酸中毒和横纹肌溶解。
一名35岁无既往病史的男性因多饮、全身乏力、头晕和持续一周的视觉障碍就诊于急诊科。检查发现他处于糖尿病酮症酸中毒状态。其糖化血红蛋白A1c为11%。患者接受了糖尿病酮症酸中毒的适当治疗,并于住院第1天病情缓解。住院第2天,患者体温升至101.6°F,精神状态严重改变,出现听觉和视觉幻觉。脑脊液(CSF)中针对西尼罗河病毒的IgM和IgG抗体呈阳性。患者住院期间肌酸激酶水平升至118,400 U/L,最终恢复至基线水平。经过11天的住院治疗,患者完全康复,无残留神经功能缺损。
在该患者中,脑脊液IgM阳性确诊为神经侵袭性WNV。患者新诊断的糖尿病可能导致了他对神经侵袭性疾病的易感性。此外,文献中此前未描述过在糖尿病酮症酸中毒背景下的WNV脑炎,该病例表明,对于出现不明原因神经症状的患者,WNV神经侵袭性疾病应列入鉴别诊断。
诊断神经侵袭性WNV对于停止不必要的治疗、限制进一步的诊断评估、帮助预测患者预后、指导公共卫生预防措施以及进一步研究界定WNV疾病谱的临床情况至关重要。