Kaloti Zaid, Bell Kendall, Khalid Mowyad, Levine Diane
Internal Medicine, Wayne State University, Detroit, Michigan, USA
Internal Medicine, Wayne State University, Detroit, Michigan, USA.
BMJ Case Rep. 2020 Mar 10;13(3):e230710. doi: 10.1136/bcr-2019-230710.
We present a case of Legionnaires' disease complicated by cerebellar ataxia. A 60-year-old man was diagnosed with Legionnaires' disease by urine antigen after presenting to the hospital with a main problem of headache and gait instability. He also had a productive cough, as well as nausea, vomiting and diarrhoea. Initial physical examination revealed a positive Romberg test, positive pronator drift, severely unsteady gait and bilateral upper extremity resting tremors with the remainder of cranial nerves and neurological examination being unremarkable. The patient had a prolonged hospital course requiring endotracheal intubation and mechanical ventilation. He received 14 days of levofloxacin with resolution of the pneumonia. On repeat assessment prior to discharge, the patient's neurological symptoms improved; however, he still had mild residual gait instability, dysdiadokinesia and difficulty with fine motor tasks such as writing. Romberg test remained positive.
我们报告一例并发小脑共济失调的军团病病例。一名60岁男性因头痛和步态不稳为主诉入院,经尿抗原检测确诊为军团病。他还伴有咳痰,以及恶心、呕吐和腹泻。初始体格检查发现闭目难立征阳性、旋前圆肌征阳性、步态严重不稳,双侧上肢静息性震颤,其余颅神经及神经系统检查未见异常。患者住院病程延长,需要气管插管和机械通气。他接受了14天的左氧氟沙星治疗,肺炎症状得到缓解。出院前复查时,患者的神经症状有所改善;然而,他仍有轻度残余步态不稳、轮替运动障碍以及书写等精细运动任务困难。闭目难立征仍为阳性。