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Synchronous rare tumors in a pediatric patient with a de novo cancer predisposition syndrome
Journal article   Peer reviewed

Synchronous rare tumors in a pediatric patient with a de novo cancer predisposition syndrome

Timothy J. D. Ohlsen, Samantha Scanlon, Francisco A. Perez, Ralph P. Ermoian, Vera A. Paulson, Jason S. Hauptman, Erin E. Crotty and Michelle A. Ting
Pediatric Blood and Cancer, Vol.69(11)
2022
DOI: https://doi.org/10.1002/pbc.29746

Abstract

Child Disease Susceptibility Genetic Predisposition to Disease Humans Neoplasms, Multiple Primary acetylsalicylic acid arginine bevacizumab histone H3 irinotecan isocitrate dehydrogenase protein p53 temozolomide transcriptional regulator ATRX abdominal radiography apparent diffusion coefficient blood brain biopsy brain damage brain stem bulbar paralysis cancer combination chemotherapy cancer patient cancer radiotherapy capsula interna case report chemoradiotherapy child clinical article copy number variation echocardiography emergency ward facial droop female fluid-attenuated inversion recovery imaging gait disorder ganglioneuroma gene inactivation genetic association genetic variability germline mutation glioblastoma glioma hemiparesis heterozygosity loss high throughput sequencing histopathology hospice care human human tissue immunohistochemistry incidental finding inoperable cancer ischemic stroke Letter Li-Fraumeni syndrome low drug dose lower limb maintenance chemotherapy MELAS syndrome molecular diagnosis multiple tumor neuroimaging neurologic disease nuclear magnetic resonance imaging occupational therapy patent foramen ovale pediatric patient pediatric physiotherapy preschool child proton therapy radiation response radiotherapy dosage repeat procedure speech therapy stereotactic biopsy T2 weighted imaging thalamus treatment failure treatment response upper limb whole genome sequencing wild type disease predisposition genetic predisposition genetics multiple cancer pathology

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