دورية أكاديمية

Treatment of Lyme neuroborreliosis with plasmapheresis

التفاصيل البيبلوغرافية
العنوان: Treatment of Lyme neuroborreliosis with plasmapheresis
المؤلفون: Çelik T., Çelik Ü., Kömür M., Tolunay O., Dönmezer Ç., Yıldızdas D.
المساهمون: Çukurova Üniversitesi
بيانات النشر: Wiley-Liss Inc.
سنة النشر: 2016
مصطلحات موضوعية: child, Guillain–Barre, Lyme, plasmapheresis
الوصف: PubMedID: 26356494 ; Lyme disease is a rare tick-borne multisystemic infection caused by Borrelia burgdorferi. Different neurological conditions were reported in the disease. In this article, we present a 15-year-old patient hospitalized with ataxia who was diagnosed with Lyme neuroborreliosis. Intravenous immunoglobulin and ceftriaxone treatment was applied to the patient for 4 weeks. However, ataxia did not recover, upper and lower muscle weakness developed, and deep tendon reflexes diminished during follow-up. The patient was diagnosed with Guillain–Barre syndrome arising from B. burgdorferi. Second dose of intravenous immunoglobulin treatment was started for 5 days but the patient didn't recover. Therefore administration of plasmapheresis was decided. All symptoms relieved following the plasmapheresis. The effect of plasmapheresis in pediatric neuroborreliosis has not been documented before. This study highlights that plasmapheresis could be a useful alternative for pediatric neuroborreliosis cases. J. Clin. Apheresis 31:476–478, 2016. © 2015 Wiley Periodicals, Inc. © 2015 Wiley Periodicals, Inc.
نوع الوثيقة: article in journal/newspaper
اللغة: English
تدمد: 0733-2459
العلاقة: Journal of Clinical Apheresis; Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı; https://dx.doi.org/10.1002/jca.21430Test; https://hdl.handle.net/20.500.12605/22245Test; 31; 476; 478
DOI: 10.1002/jca.21430
الإتاحة: https://doi.org/20.500.12605/22245Test
https://doi.org/10.1002/jca.21430Test
https://hdl.handle.net/20.500.12605/22245Test
حقوق: info:eu-repo/semantics/closedAccess
رقم الانضمام: edsbas.D8ACF40F
قاعدة البيانات: BASE
الوصف
تدمد:07332459
DOI:10.1002/jca.21430