Abstract:Posterior reversible encephalopathy syndrome features reversible cortical neurologic dysfunction and characteristic findings on brain imaging studies. This syndrome can be caused by several agents including traditional chemotherapy and immunosuppressive drugs. Targeted therapies such as agents binding vascular endothelial growth factor/VEGFR, CD20 and cytotoxic T-cell lymphocyte antigen 4 (CTLA-4) antigens are also among the culprits. Vemurafenib is a BRAF gene inhibitor that has not been previously linked wit… Show more
“…Erythropoietin and certain colony stimulating factors such as G-CSF have been associated with PRES as well. This syndrome has also been reported to be associated with newer targeted therapies such as antivascular endothelial growth factor (VEGF) agents (bevacizumab), A B anti-CD20 antibodies (rituximab), tyrosine kinase inhibiting (TKI) agents (sorafenib, sunitinib, pazopanib) and, most recently, with anti-cytotoxic T-cell lymphocyte antigen 4 (CTLA-4) agents (ipilimumab) (24).…”
Section: Discussionmentioning
confidence: 99%
“…This as a domino phenomenon triggers mild and reversible ischemia and oedema of the white matter (23). Moreover, chemotherapeutic agents (MTX, L-asparaginase, adriamycin, cyclophosphamide, cytosine arabinoside, vincristine) contribute to PRES also by inducing or exacerbating hypertension due to corticosteroids treatment or renal dysfunction (24). Erythropoietin and certain colony stimulating factors such as G-CSF have been associated with PRES as well.…”
“…Erythropoietin and certain colony stimulating factors such as G-CSF have been associated with PRES as well. This syndrome has also been reported to be associated with newer targeted therapies such as antivascular endothelial growth factor (VEGF) agents (bevacizumab), A B anti-CD20 antibodies (rituximab), tyrosine kinase inhibiting (TKI) agents (sorafenib, sunitinib, pazopanib) and, most recently, with anti-cytotoxic T-cell lymphocyte antigen 4 (CTLA-4) agents (ipilimumab) (24).…”
Section: Discussionmentioning
confidence: 99%
“…This as a domino phenomenon triggers mild and reversible ischemia and oedema of the white matter (23). Moreover, chemotherapeutic agents (MTX, L-asparaginase, adriamycin, cyclophosphamide, cytosine arabinoside, vincristine) contribute to PRES also by inducing or exacerbating hypertension due to corticosteroids treatment or renal dysfunction (24). Erythropoietin and certain colony stimulating factors such as G-CSF have been associated with PRES as well.…”
“…Magnetic resonance imaging (MRI) evidence of hyperintense signal change in the cortical–subcortical areas, typically in posterior circulation distribution, is required to confirm PRES diagnosis . Initially described in hypertensive encephalopathy and eclampsia, subsequent reports have suggested an association with drugs, particularly immune system and vascular endothelial system modulating agents . Outcome of PRES in noncancer patients is usually good, but permanent sequelae and life‐threatening complications have been described .…”
Section: Introductionmentioning
confidence: 99%
“…[1,2] Initially described in hypertensive encephalopathy and eclampsia, subsequent reports have suggested an association with drugs, particularly immune system and vascular endothelial system modulating agents. [3][4][5] Outcome of PRES in noncancer patients is usually good, but permanent sequelae and life-threatening complications have been described. [6,7] Reports on outcomes of PRES in children with cancer have been limited by small number of patients and inadequate follow-up data.…”
Background
Diagnosis of posterior reversible encephalopathy syndrome (PRES) requires presence of headache, seizures, impaired vision, or altered mentation accompanied by specific imaging findings. We aimed to study long-term clinical and radiologic outcome of PRES in children with cancer to augment limited available data.
Procedure
Retrospective review of children with cancer who were diagnosed with PRES.
Results
We identified PRES in 21 males and 16 females amongst the 5,217 children treated during the study period. Median time from cancer diagnosis to PRES was 6.6 months in 25 leukemia (1.6%), 5 brain tumor (0.3%), and 7 other solid tumor (0.4%) patients; p=<0.0001 for leukemia versus all other tumors. Symptoms included seizures (97%), headaches (40%), altered mentation (68%), and vision impairment (27%). Hypertension in 97% and steroids use was seen in 78%. Headaches, visual disturbance, and mental status resolved within a median of <3 days, while epilepsy developed in 19%. T2 hyperintense signal was present in 100% of occipital, 47% of temporal, 75% of parietal, and 55% of frontal lobes, as well as 22% of cerebellum and 5% of basal ganglia. Follow-up MRI in 34 patients showed partial or complete T2 resolution in 79%, development of laminar necrosis in 5, microhemorrhages in 6, and focal atrophy in 3.
Conclusion
PRES in children is more common in hematological malignancy compared to other tumors and is associated with hypertension and steroid use. Seizure is the most common acute manifestation. Most MRI changes resolve, but persistent imaging abnormality and epilepsy may develop in a significant minority.
“…To the best of our knowledge, there are only four case reports on PRES under novel melanoma treatments [8][9][10][11]. However, the diagnosis of PRES in these cases was not completely reliable because an MRI was not performed [8,10].…”
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