Review
Copyright ©The Author(s) 2016.
World J Clin Pediatr. Aug 8, 2016; 5(3): 262-272
Published online Aug 8, 2016. doi: 10.5409/wjcp.v5.i3.262
Table 5 Summarizes incidentally found “serious lesions” on pediatric brain magnetic resonance imaging
Ref.The context in which brain MRI was orderedWorsening course
Outcome/comment
KnownPotential
Yilmaz et al[5]Children mean age 11.2 yr presented for headache evaluationMalignant brain tumor and hydrocephalusChiari I malformation I; Relevant to headacheTissue type of tumor in study was unspecified
Schwedt et al[8]Children mean age 12.1 yr presented for headache evaluationTumors, moyamoya disease, and demyelinating diseaseArteriovenous malformation and intracerebral hemorrhageStudy focus was “benign” imaging abnormalities, no further information for serious lesion other than pineal tumor was available
Kalnin et al[10]Children mean age 9.7 yr presented for the first onset seizureNoneTemporal lobe lesionsVarious Epileptic abnormalities1 have been associated with pediatric brain MRI
Potchen et al[14]Community-based children mean age 12.1 yrGranulomas with gliosisEmpty sella and vermian atrophyCalcified granulomas caused by neurocysticercosis or tuberculosis occurs in the endemic part of the world
Mogensen et al[19]All girls, mean age unavailable, presented for early puberty evaluation to endocrine clinicPontine and pineal tumor, and hypothalamic pilocytic astrocytomaHydrocephalus, cortical dysplasia, and chiari II malformationA high frequency a pathological brain findings occurred in 6-8 yr old girls with precocious puberty
2Perret et al[20]Incidentally found mass lesions management in children mean age 7.6 yr in oncologyLow-grade glioma, craniopharyngioma, ependymoma, and CPPMedulloblastoma and fibrillary astrocytomaDysembryoplastic neuroepithelial tumor and tectal glioma can be monitored conservatively
Jordan, et al[21]Children mean age 9.2 yr with sickle cell disease in neurology researchChiari I malformation with large spinal cord syrinx3Possible tectal glioma, Possible tumor vs dysplasiaAmongst 6.6% incidental findings identified, 0.6% children with sickle cell disease had potentially serious or urgent finding