Fetal heart/chest pathology registry review Flashcards

(41 cards)

1
Q

Hypoplastic left heart

A

Small or absent left ventricle. Surgery must be preformed within 1st month of life

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2
Q

Leading cause of cardiac death in neonate

A

Hypoplastic left heart

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3
Q

Cardiac view of hypoplastic left heart and possible causes

A

-4CH with small or absent left ventricle
- Aortic atresia, aortic stenosis, coarctation
-Connection with T13

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4
Q

Hypoplastic right heart

A

Small or absent right ventricle

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5
Q

Cause of hypoplastic right heart

A

Pulmonary stenosis or tricuspid atresia

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6
Q

Cardiac view of hypoplastic right heart and additional findings

A

-Small/absent right ventricle, enlarged left ventricle
-Fetal hydrops

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7
Q

Hydrops fetalis

A

Accumulation of fluid in 2 fetal body cavities

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8
Q

Cause of hydrops fetalis

A

Heart failure, tumors, syndromes, ect

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9
Q

Ventricular septal defects (VSD)

A

Opening or hole in ventricular septum; may be isolated or associated with other defects

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10
Q

Most common cardiac defect

A

Ventricular septal defect

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11
Q

Cardiac view of ventricular septal defects

A

4CH with beam perpendicular to IVS, showing “gap” with color flow crossing the septum

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12
Q

Arterial septal defects (ASD)

A

Absence of segment of atrial septum (*foramen ovale should normally be seen as a large opening in septum)

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13
Q

Atrioventricular septal defects
(endocardial cushion defect or AV canal defect)

A

Lack of development of central part of heart
Associated with T21

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14
Q

Endocardial cushion

A

Where the IVS, IAS, septal valve leaflets connect at the center

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15
Q

Cardiac view of atrioventricular septal defects

A

4CH absence of atrial/ventricular septum. Lack of apical offset to mitral valve and tricuspid valve

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16
Q

Ebstein Anomaly

A

Tricuspid valve is incorrectly positioned apically within the right ventricles, atrialized right ventricle, poor prognosis

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17
Q

Atrialized

A

A condition where part of the right ventricle becomes functionally part of the right atrium

18
Q

Cardiac view of ebstein anomaly

A

4CH malpositioned tricuspid valve, tricuspid regurfitation, enlarged right atrium

19
Q

Tetralogy of Fallot

A

Combination of 4 findings: overriding aorta, VSD, pulmonary stenosis, RV hypertrophy

20
Q

Cardiac vies of tetralogy of fallot

A

4CH and outflow tracts

21
Q

Rhabdomyoma

A

Echogenic tumors within myocardium; associated with tuberous sclerosis, cardiac failure, fetal hydrops

22
Q

Most common fetal cardiac tumor

23
Q

Tuberous sclerosis

A

Tumors on multiple organs

24
Q

Echogenic intracardiac focus (EIF)

A

Calcification of papillary muscle or chordae tendonae usually seen in left ventricle

25
Ectopia Cordis
Heart located outside the chest through defect in sternum; elevated AFP
26
Transposition of great vessels
Great vessels aorta and main pulmonary artery are switched -Aorta rises from right ventricle -Main pulmonary artery arises from left ventricle
27
Coarctation of aorta
Narrowing of aortic arch, commonly between left subclavian artery and ductus arteriosus
28
Associated findings with coarctation of aorta
Right ventricle and main pulmonary artery enlargement
29
Cardiac views of coarctation of aorta
Outflow tracts, sagittal aortic arch, possibly normal 4CH
30
Pericardial effusion
Fluid located AROUND the heart
31
Pleural effusion
Fluid surrounding lungs *bat wing sign = bilateral effusion
32
Pulmonary hypoplasia
Underdevelopment of lungs *result of other defects
33
Most common cause of chest mass causing pulmonary hypoplasia / reason for cardiac malposition
Diaphragmatic hernia
34
Diaphragmatic hernia
A birth defect in which there is an abnormal opening in the diaphragm
35
Bochdalek hernia
Most common on left side; containing stomach, bowel and left lobe of liver -No stomach will be seen in the abdomen -Heart pushed to the right, stomach lateral to heart
36
Right diaphragmatic hernia
Through foramen of Morgagni may allow entire liver into chest. -Heart pushed to left
37
Congenital pulmonary airway malformation (CCAM)
Mass consisting of abnormal bronchial and lung tissue. Causes displacement of heart to contralateral side -Normally regress spontaneously -Large can lead to hydrops or pulmonary hypoplasia
38
Type 1 congenital pulmonary airway malformation
Most common type. Macrocystic, large visualized cysts
39
Type 2 congenital pulmonary airway malformation
Mixed, cystic and solid appearing
40
Type 3 congenital pulmonary airway malformation
Microcystic. Cysts too small to be visualized, entire mass is echogenic. Similar appearance as pulmonary sequestration
41
Pulmonary sequestration
Echogenic mass of nonfunctioning lung tissue with own blood supply or arises from thoracic aorta