PEDS NEURO
CONGENITAL MALFORMATIONS
DWM: large post fossa w upward displacement of tentorium & elevation of torcular herophili (torcular-lamboid inversion), severe vermian hypoplasia (agenesis), cystic dilatation of 4th ventricle, communication of the 4th ventricle to the posterior fossa cyst. When not ALL of these findings are seen, use the term DW variant. 80% have hydrocephalus.
Callosal dysgenesis: CC forms genu -> splenium; assoc pericallosal lipoma
Holoproscencephaly: large supratentorial dorsal cyst (alobar) w/ downward mass effect on post fossa
Mega cisterna magna: normal 4th ventricle covere by an intact cerebellar vermis, normally positioned tentorium
C2M: small posterior fossa w inferior herniation of intact cerebellar vermis
MASSES
DDX: age? intraventricular or intraparenchymal? supra or infratentorial?
Ependymoma: 15% of peds post fossa tumor; ages 1-5; 2/3 occur in post fossa (intraventricular floor)& 1/3 in preventricular supratentorial WM, -restricted diffusion; More likely to contain foci of hemorrhage or calcification compared to other pediatric 4th ventricle mass; <20% of pts develop CSF mets; Assoc NF2; surgical resection is primary tx +/- chemorads (never <3 yo)
Medulloblastoma: Age 6-11 yo; hyperdense NECT, classically arises from 4th ventricle roof in midline post fossa; no extension through foramen of Magendie/Luschka; T2WI isointense; intraventricular/roof, +restricted diffusion, >90% enhancement; typically little cyst component
ATRT: <3 yo; off-midline & CPA; 40% are supratentorial; NECT hyperdense; restricted diffusion w/o cystic components dismal prognosis
JPA: MC primary; Peak age 5-15 yo; 60% cerebellum, 25% optic chiasm; variable appearance; solid heterogeneously enhancing mass; off-midline post fossa mass largely composed of a cyst w an enhancing mural nodule arising from cerebellar hemisphere; less frequently includes a centrally necrotic solid mass or a solid mass w/o cyst; no restricted diffusion; Increased enhancement
Assoc w NF1 (particularly in optic pathway and brainstem)
Tx w surgery
Brain stem glioma: pons, +restricted diffusion, +/- enhancement (better if NF1)
Choroid plexus carcinoma: hyperenhancing mass arising MC lateral ventricular atria in children & rarely in post fossa(4th ventricle in adults)
Hemangioblastoma: hx of vHL
OTHER
Acute encephalitis: Neonatal affects any lobe, older children affects inf frontal & temporal lobes; cytotoxic edema w/ GWD loss
HEAD & NECK

SPINAL ULTRASOUND
Spinal lipoma: echogenic mass
Tethered SC: low conus medullaris (below L3) with possible short thickened filum terminale; assoc dorsal displacement of SC, decreased SC pulsatility, intrathecal cyst
If not diagnosed in newborn period, may present later in childhood w incontinence, lower extremity spasticity, weakness, &/or scoliosis.
Dorsal dermal sinus: tract extension from dimple to thecal sac
Diastematomyelia: split in SC or fibroosseous spur
Myelomeningocele: obvious sac protruding through a dysraphic defect
CASES
