neonatal brain 3 Flashcards

(39 cards)

1
Q

what is hydrocephalus

A

progressive dilation of ventricular system

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2
Q

3 mechanisms leading to hydro cephalic

A

Obstruction to CSF outflow
Decreased CSF absorption
CSF overproduction

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3
Q

what grades of hemorrhage can cause hydrocephalus

A

3 and 4

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4
Q

what are 3 signs of hydrocephalus

A

Increasing head size
Bulging of the anterior fontanelle
Separation of cranial sutures

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5
Q

what can occur later with hydro cephalic

A

Bradycardia, apnea and increased ICP

thus monitoring is important

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6
Q

what is ependymitis

A

swelling of the ependymal linings of the ventricles.

it will have increased echogenicity

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7
Q

infants with progressive hydrocephalus and increased ICP may require

A

shunt

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8
Q

what is done to identify ICP

A

a slight pressure is applied to the head with using spectral doppler of pericallosal artery

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9
Q

does cerebellar hemorrhage have crazy symptoms

A

no it may be silent and just found out of routine

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10
Q

how is cerebral hemorrhage viewed

A

through mastoid fontanelle

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11
Q

normal posterior fossa viewed through

A

mastoid fontanelle

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12
Q

what will hemorrhage appear as

A

large echogenic space

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13
Q

what is periventricular leukomalacia

A

hypoxic ischemic brain injury

leukomalacia means softening of white tissue

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14
Q

common sites of periventricular leukomalacia

A

White matter adjacent to peritrigonal area of lateral ventricles
Frontal cerebral white matter anterolateral to frontal horns

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15
Q

sono appearance of PVL

A

Increased echogenicity in affected area
Bilateral and symmetric
Echogenicity should not be > choroid plexus
Difficult to differentiate from periventricular blush
Later changes to PVL
Formation of cysts as a result of necrosis and cavitation

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16
Q

long term effects of PVL

A

cerebral palsy, developmental abnormalities, intellectual and visual impairment

17
Q

appearance of agenesis of corpus callosum

A

Frontal horns widely separated and angled laterally
Occipital horns have parallel orientation and a teardrop* shape
Enlargement of posterior (occ.) horns (colpocephaly)
*
Radial arrangement of sulci and gyri above 3rd ventricle – sunburst sign**
Absent CSP*, high and enlarged 3rd ventricle

18
Q

dandy walker malformation has a spectrum of anomalies affecting

A

posterior fossa

19
Q

7 anomalies of dandy walker malformations

A
Cystic dilatation of 4th ventricle
Superior elevation of the tentorium
Absence of vermis
Small cerebellar hemispheres
Hydrocephalus 
agenesis of CC
holoprosencephaly
20
Q

most common type of chiari malformation

21
Q

what is chiari malformation almost always associated with

A

myelomenigocele

22
Q

what is seen when the 3rd ventricle is dilated and what does it connect

A

massa intermedia

connects two thalami and crosses the third ventricle

23
Q

several sono appearance of chiari malformation

A

Hydrocephalus with prominent massa intermidia
Inferior pointing of frontal horns – “bat wing”
Downward displacement of cerebellum and 4th v. into spinal canal
Non-visualized cisterna magna
Small posterior fossa
Low and displastic tentorium
Colpocephaly (large occ. horns)
Complete or partial CC agenesis

24
Q

coronal plane sign of chiari 2 malformation

A

bat wing appearance

25
most common intracranial vascular anomaly in neonate
vein of galen malformation
26
what is vein of galen malformation
midline cerebral AV malformation that causes dilatation of v. of Galen Anterior and posterior cerebral arteries feed the malformation Decreased blood supply to brain – atrophy and calcifications of brain
27
what sono signs are seen with vein of galen malformation
cystic structure turbulent flow increased systolic and diastolic flow velocities
28
what is holoprosencephaly
Spectrum of congenital malformations that result from a disorder of diverticulation in which the primitive forebrain (prosencephalon) fails to divide into two separate cerebral hemispheres
29
most severe holoprosencephaly
most severe | alobar type are stillborn or die shortly after birth
30
facial defects as a result of alobar holoprosencephaly
``` Severe facial anomalies Close set eyes – hypotelorism Cyclopia Proboscis – nose on forehead Cleft lip/palate ```
31
brain defects as a result of alobar
``` There is a thin pancake like primitive cerebrum covering a horseshoe shaped midline monoventricle Missing: Corpus callosum Third ventricle Interhemispheric fissures Thalami are fused ```
32
semilobar brain defects
Incomplete forebrain division with partial separation of the cerebral hemispheres posteriorly Single ventricle with occipital and temporal horns formed Falx may be present 3rd v. is small or absent
33
intracranial infections torch acronym
``` T  Toxoplasmosis O  Others R  Rubella C  Cytomegalovirus CMV H  Herpes Simplex ```
34
most common intracranial infection
CMV
35
2nd mots common intracranial infection
toxoplasmosis
36
intracranial infections transmit how
via placenta | except herpes is transmitted at birth
37
role of US with intracranial infections
observe Parenchymal calcifications and Lenticulostriate vasculopathy
38
what is seen sono with CMV
non shadowing echogenic foci representing parenchymal calcifications
39
what is seen on sonogram with lenticulostriate vasculopathy
Bilateral branching of echogenic foci in the basal ganglia (these are mineral deposits)