M Baig Mirza, Phillips Martin
Department of Internal Medicine , Kankakee, IL, USA.
Department of Infectious Diseases, Riverside Medical Center , Kankakee, IL, USA.
Infect Dis Rep. 2013 Oct 14;5(2):e10. doi: 10.4081/idr.2013.e10. eCollection 2013 Oct 9.
Creutzfeldt-Jakob disease (CJD) is a rapidly progressive and ultimately fatal disorder of the central nervous system. It occurs worldwide with an incidence of 0.5-1 new case per million population per year. No specific treatment is available and management is limited to supportive care. Autopsy or biopsy provides a definitive diagnosis. Because of the transmissible nature of the disease and hesitancy of patients/family members to give consent for biopsy, numerous challenges in confirming the clinical diagnosis are faced by healthcare professionals. We report a case of 66-year-old male who was hospitalized due to hip fracture following a fall. Acute mental status changes followed the surgical fixation of hip fracture which triggered neurologic work up. This finally revealed suspicion and confirmation of CJD. Patient had progressive cognitive decline with akinetic mutism during further hospital stay and was later discharged home with hospice. Shorter thereafter he died at home. This case demonstrates the importance of keeping an open mind towards possibility of CJD when faced with esoteric neurologic presentations. Also this case provides insight into challenges in quarantine and sterilization of surgical instruments when these patients go through major surgeries.
克雅氏病(CJD)是一种中枢神经系统快速进展且最终致命的疾病。它在全球范围内均有发生,每年每百万人口的发病率为0.5 - 1例新发病例。目前尚无特效治疗方法,治疗仅限于支持性护理。尸检或活检可提供确诊依据。由于该疾病具有传染性,且患者/家属对活检同意存在犹豫,医护人员在确诊临床诊断时面临诸多挑战。我们报告一例66岁男性患者,因跌倒后髋部骨折入院。髋部骨折手术固定后出现急性精神状态改变,进而引发神经系统检查。最终怀疑并确诊为克雅氏病。患者在进一步住院期间出现进行性认知衰退及缄默症,随后在家中接受临终关怀出院。此后不久,他在家中去世。该病例表明,面对罕见的神经系统表现时,对克雅氏病的可能性保持开放态度非常重要。此外,该病例还揭示了这些患者接受大手术时,手术器械的隔离和消毒所面临的挑战。