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Posterior reversible leukoencephalopathy syndrome in children with hematologic disorders.
Malbora, Baris; Avci, Zekai; Dönmez, Fulden; Alioglu, Bülent; Baskin, Esra; Alehan, Füsun; Özbek, Namik.
Afiliación
  • Malbora B; Baskent University Faculty of Medicine, Department of Pediatric Hematology 6. Cadde, No: 72/3, 06490, Bahçelievler 06490 Ankara, Turkey Phone: +90 312 212 68 68 E-mail: barismalbora@gmail.com.
Turk J Haematol ; 27(3): 168-76, 2010 Sep 05.
Article en En | MEDLINE | ID: mdl-27263601
ABSTRACT

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.

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Tipo de estudio: Prognostic_studies / Screening_studies Idioma: En Revista: Turk J Haematol Año: 2010 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Tipo de estudio: Prognostic_studies / Screening_studies Idioma: En Revista: Turk J Haematol Año: 2010 Tipo del documento: Article