Pregled bibliografske jedinice broj: 1259011
West Nile virus presenting as opsoclonus-myoclonus cerebellar syndrome
West Nile virus presenting as opsoclonus-myoclonus cerebellar syndrome // 29th ECCMID 2019
Amsterdam, Nizozemska, 2019. P0043, 1 (poster, međunarodna recenzija, sažetak, znanstveni)
CROSBI ID: 1259011 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
West Nile virus presenting as opsoclonus-myoclonus
cerebellar syndrome
Autori
Vukelić, Dalibor ; Zember, Sanja ; Oroši, Dorotea
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Skup
29th ECCMID 2019
Mjesto i datum
Amsterdam, Nizozemska, 13.04.2019. - 16.04.2019
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
West Nile virus ; opsoclonus-myoclonus cerebellar syndrome
Sažetak
Background: West Nile virus (WNV) first appeared in the Western hemisphere in 1999 with an outbreak in the New York City area. Most individuals infected with WNV remain asymptomatic. Susceptibility increases with age, chronic illness, and immunosuppression. WNV most commonly causes meningitis and meningoencephalitis, however it can also cause acute flaccid paralysis, as well as focal parenchymal involvement of the cerebellum, brainstem, rhombencephalon, or spinal cord. Case report: We presenta case of a 70-year- old patient admitted to the University Hospital for Infectious Diseases on the 6th day of illness, that started with fever and headache, and from the 3rd day accompanied by vommiting and diarrhea. The patient had diabetes mellitus and ten years ago underwent hysterectomy due to carcinoma in situ. Additional therapy was not needed. On admission to the hospital, the patient had a temperature of 39 °C. There was mild neck stiffness. She was alert and fully oriented, with a mild truncal and limb ataxia, mild myoclonus and opsoclonus/ocular flutter. Lumbar puncture revealed mononuclear pleocytosis in the cerebrospinal fluid (CSF). Differential etiology ruled out herpes simplex virus, enteroviruses, lysteria, tick borne encephalitis, B.burgdorferi. Paired serology testing confirmed West-Nilevirus. WNV viruria was also confirmed by PCR. The virus was not detected in the CSF. Paraneoplastic/autoimmune etiology of encephylitis was also ruled out as well as malignant disease dissemination. With symptomatic and supportive theray, the patient became afebrile and her headache resolved. Opsoclonus/ocular flutter was expressed for more than a month, after which it gradually abated. Conclusions: West-Nile virus infections have been recorded in Croatia since 2012. The majority of cases have been confirmed in 2018 (more than 50 cases so far). At the Zagreb University Hospital for Infectious Diseases, 12 patients have been treated in the past 6 months with clinical presentation of meningoencephalitis, of whom three died. We present a case of opsoclonus-myoclonus cerebellar syndrome caused by WNV in a 70-year-old patient with favorable disease outcome. To our knowledge, there have been only two other reported cases of opsoclonus myoclonus cerebellar ataxia due to WNV infection.
Izvorni jezik
Engleski
Znanstvena područja
Kliničke medicinske znanosti
POVEZANOST RADA
Ustanove:
Medicinski fakultet, Zagreb,
Klinika za infektivne bolesti "Dr Fran Mihaljević"