Fig. 22.1
(a) Axial brain MRI T1WI with contrast showing an irregularly enhancing posterior fossa fourth ventricular lesion in a child with recurrent ependymoma with spinal metastases. (b) Sagittal T1WI + C of a 4-year-old child with progressive headache and no neurologic deficit, showing a large 4-cm mass enhancing mass within the fourth ventricle
Fig. 22.2
(a) Brain MR and T1 contrast weighted coronal sequence showing a left lateral ventricle choroid plexus papilloma. Fifteen-year-old boy, incidentally found to have this tumor after a mild traumatic brain injury. (b) Axial T1WI + C of the patient in Fig. 22.1a showing metastatic ependymoma along the CSF pathways to settle in the right frontal horn
Epidemiology and Classification
Brain tumors are the most common form of solid cancer in the pediatric population/childhood. Their incidence has increased within the past few decades, with a current annual age-adjusted rate of 3.2 cases per 100,000 children, as reported by the Cancer Statistics Report (CSR).
Pediatric brain tumors are primary classified by their location within the intracranial compartments in infratentorial and supratentorial tumors . About 60 % of brain tumors in children occur in the infratentorial compartment, and they may be intrinsic to the brain stem (Fig. 22.3) or located with the cerebellar parenchyma or cerebrospinal fluid spaces of the posterior fossa (Fig. 22.4). Supratentorial tumors are usually hemispheric (Fig. 22.5) but may also arise from the suprasellar and/or pineal region (Fig. 22.6). For the youngest children, the ratio of infratentorial versus supratentorial lesions is reversed, and in the first year of life, supratentorial tumors are actually slightly more prevalent.
Fig. 22.3
(a) Brain MRI sagittal T2WI showing an expansile pontine mass that abuts the clivus in a 7-year-old girl presenting with hemiparesis; (b, d) encasing the basilar artery in axial T2WI. The actual size and extension of such lesions are more readily detected on axial FLAIR images; (c) in a 14-year-old child with ocular motility problems
Fig. 22.4
(a) Axial T1WI + C in a 13-year-old child presenting with headache and progressive ataxic gait. It shows a well-defined partially cystic contrast-enhancing lesion in the left cerebellar hemisphere. Common site and configuration for JPA. (b) Axial T1WI + C of an 11-year-old boy with classic cerebellar manifestations of headache, nausea, and vomiting, showing an irregular ring-enhancing lesion with a more solid component to one side. Also a classic picture and presentation of juvenile pilocytic astrocytoma (JPA)
Fig. 22.5
(a) Brain MRI, T2WI axial sequence showing a left hemispheric desmoplastic infantile astrocytoma. Three-month-old boy that presents with a new onset seizure. (b) Axial T1WI + C MRI brain of a child with multiple recurrent astrocytoma GIV presenting with progressive headache, lethargy, and worsening inactivity
Fig. 22.6
(a) Sagittal T1WI + C of a 17-year-old child with incidental diagnosis of this lesion. Had no hormonal or visual problems, no clinical evidence of diabetes insipidus. He has a contrast-enhancing sellar mass with suprasellar partially cystic extension (white arrow head). (b) Brain MRI T2WI sagittal sequence showing a pineal region immature teratoma. Two-month-old girl that presented with a bulging anterior fontanel, sunset gaze, and emesis
The World Health Organization (WHO) outlines another important classification. This is based upon a tumor’s behavior and its histopathological characteristics. Inside the infratentorial compartment, the most typical histological subtypes are cerebellar astrocytomas, medulloblastomas, ependymomas (Figs. 22.7 and 22.8), and brain stem gliomas. In the supratentorial space, gliomas and particularly low-grade astrocytomas (Fig. 22.9) remain the most common tumors of the cerebral hemispheres. Craniopharyngiomas (Fig. 22.10) and optic pathway gliomas of the suprasellar region and germ cell tumors of the pineal region are also fairly common.
Fig. 22.7
(a) Brain MRI T1WI + C sagittal sequence showing a fourth ventricle medulloblastoma. Ten-year-old boy that presented with a several-month history of emesis and headaches. (b) Axial T1WI + C of 4-year-old child with progressive headache shown in Fig. 22.1b with posterior fossa ependymoma