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Posterior reversible encephalopathy syndrome in children with cancer.

Posterior reversible encephalopathy syndrome in children with cancer. Research Abstract Details 

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  • Posterior reversible encephalopathy syndrome in children with cancer. Abstract Text:

    e brannon morrisE Brannon Morris,fred h laninghamFred H Laningham,john t sandlundJohn T Sandlund,raja b khanRaja B Khan,

    PURPOSE: To identify predisposing factors, radiologic features, and clinical outcome of posterior reversible leucoencephalopathy (PRES) in children receiving cancer treatment. METHODS: We identified 11 patients (7 female) who had radiological and clinical features consistent with PRES and were treated for cancer at St. Jude Children's Research Hospital between January 1995 and January 2005. Clinical and radiographic data were abstracted from their records. RESULTS: The average age at the time of PRES onset was 10.4 years. Primary diagnoses were acute leukemia (n = 8), non-Hodgkin lymphoma (n = 2), and Ewing sarcoma (n = 1). PRES occurred in 8 patients during the induction phase of treatment, and all 11 patients had hypertension (5 chronically). Seizure activity was proximate to cytarabine and tacrolimus administration in three patients and further seizures occurred with re-administration of these medications in two patients. Coagulation and chemistry studies were normal. Concurrent brain magnetic resonance imaging (MRI) demonstrated T2 signal abnormalities in all 11 patients, restricted diffusion in 4, and hemorrhage in 3. Follow-up MRI showed chronic changes consistent with a previous hemorrhage in three and evidence of prior parenchymal ischemia in one. Three patients developed epilepsy and remain on chronic anticonvulsant therapy. CONCLUSIONS: PRES is an increasingly recognized complication of pediatric cancer treatment. Risk factors for PRES in pediatric cancer patients include hypertension (not necessarily acute), remission induction chemotherapy, and administration of tacrolimus. MR images often show atypical findings, some of which are irreversible. A significant number of patients develop epilepsy despite clinical and radiographic evidence of recovery.

    Posterior reversible encephalopathy syndrome in children with cancer. Publishing Authors By Initials

    eb morrisEB Morris,fh laninghamFH Laningham,jt sandlundJT Sandlund,rb khanRB Khan,

    For similar pathological conditions, signs and symptoms: pathologic processes: disease: syndrome research abstracts see: pathological conditions, signs and symptoms: pathologic processes: disease: syndrome research

    PUBMED ID PMID:

    MEDLINE DATE:

    Posterior reversible encephalopathy syndrome in children with cancer. Journal Published:

    PUBLICATION TYPE: Research Support, Non-U.S. Gov

    Journal: Pediatric blood & cancer

    VOLUME: 48

    Page Numbers: 152-9

    Journal Abbreviation:

    ISSN: 1545-5009

    DAY: 3

    MONTH: Feb

    YEAR: 2007

    Posterior reversible encephalopathy syndrome in children with cancer. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 101186624

    Posterior reversible encephalopathy syndrome in children with cancer. Keywords Mesh Terms:

    KEYWORDS: Syndrome

    MESH TERMS: etiology

    Chemical & Substance for Abstract: Posterior reversible encephalopathy syndrome in children with cancer. Information

    Substance Name:

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    Grant and Affiliation Information for Posterior reversible encephalopathy syndrome in children with cancer.

    AFFILIATION: Division of Neurology, St. Jude Children's Research Hospital, Memphis, Tennessee 38105, USA. brannon.morris@stjude.org

    Country: United States

    United States Research PublicationUnited States Research Publication

    AGENCY: United States NCI

    GRANT: CA21765

    ACRONYM: CA

    MEDLINETA: Pediatr Blood Cancer

    REFSOURCE:

    DATABASENAME:

    ACCESSION NUMBER:

    Number Hits: 0

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