دورية أكاديمية

Posterior reversible leukoencephalopathy syndrome in children with hematologic disorders

التفاصيل البيبلوغرافية
العنوان: Posterior reversible leukoencephalopathy syndrome in children with hematologic disorders
المؤلفون: Barış Malbora, Zekai Avcı, Fulden Dönmez, Bülent Alioğlu, Esra Baskın, Füsun Alehan, Namık Özbek
المصدر: Turkish Journal of Hematology, Vol 27, Iss 3, Pp 168-176 (2010)
بيانات النشر: Galenos Publishing House, 2010.
سنة النشر: 2010
المجموعة: LCC:Diseases of the blood and blood-forming organs
مصطلحات موضوعية: acute leukemia, aplastic anemia, posterior reversible leukoencephalopathy syndrome, tumor lysis syndrome, Diseases of the blood and blood-forming organs, RC633-647.5
الوصف: OBJECTIVE: : Posterior reversible leukoencephalopathy syndrome (PRES) is characterized by headache, altered mental status, cortical blindness, and seizures associated with neuroradiological findings. It involves predominantly white matter of the parieto-occipital lobes. Several medications and disorders play a role in the etiology of PRES. In this study, we aimed to show how the prognosis of PRES in hematological diseases of childhood might be according to the etiological factors. METHODS: Here, we report PRES in six patients, aged 4 to 14 years, with diagnoses of leukemia and aplastic anemia. RESULTS: Suggested causes in our patients were chemotherapeutics, hypertension, infection and antimicrobial drug administration, tumor lysis syndrome, acute renal failure and hemodialysis, immunosuppressive drug administration, and hypomagnesemia. One of the patients died of sepsis, renal failure and pulmonary hemorrhage and another died of relapse after total recovery from PRES. The other four patients are under follow-up without problems. CONCLUSION: We suggest that PRES can recover fully with early diagnosis and treatment whereas it can show poor prognosis depending on the etiology.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 1308-5263
Relation: https://jag.journalagent.com/z4/download_fulltext.asp?pdir=tjh&un=TJH-62681; https://doaj.org/toc/1308-5263
DOI: 10.5152/tjh.2010.24
URL الوصول: https://doaj.org/article/bebabb34c37549e984edac8c736a9350
رقم الأكسشن: edsdoj.bebabb34c37549e984edac8c736a9350
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:13085263
DOI:10.5152/tjh.2010.24