Fetal heart/chest pathology registry review Flashcards

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

A

Rhabdomyoma

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
Q

Ectopia Cordis

A

Heart located outside the chest through defect in sternum; elevated AFP

26
Q

Transposition of great vessels

A

Great vessels aorta and main pulmonary artery are switched
-Aorta rises from right ventricle
-Main pulmonary artery arises from left ventricle

27
Q

Coarctation of aorta

A

Narrowing of aortic arch, commonly between left subclavian artery and ductus arteriosus

28
Q

Associated findings with coarctation of aorta

A

Right ventricle and main pulmonary artery enlargement

29
Q

Cardiac views of coarctation of aorta

A

Outflow tracts, sagittal aortic arch, possibly normal 4CH

30
Q

Pericardial effusion

A

Fluid located AROUND the heart

31
Q

Pleural effusion

A

Fluid surrounding lungs
*bat wing sign = bilateral effusion

32
Q

Pulmonary hypoplasia

A

Underdevelopment of lungs
*result of other defects

33
Q

Most common cause of chest mass causing pulmonary hypoplasia / reason for cardiac malposition

A

Diaphragmatic hernia

34
Q

Diaphragmatic hernia

A

A birth defect in which there is an abnormal opening in the diaphragm

35
Q

Bochdalek hernia

A

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
Q

Right diaphragmatic hernia

A

Through foramen of Morgagni may allow entire liver into chest. -Heart pushed to left

37
Q

Congenital pulmonary airway malformation (CCAM)

A

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
Q

Type 1 congenital pulmonary airway malformation

A

Most common type. Macrocystic, large visualized cysts

39
Q

Type 2 congenital pulmonary airway malformation

A

Mixed, cystic and solid appearing

40
Q

Type 3 congenital pulmonary airway malformation

A

Microcystic. Cysts too small to be visualized, entire mass is echogenic. Similar appearance as pulmonary sequestration

41
Q

Pulmonary sequestration

A

Echogenic mass of nonfunctioning lung tissue with own blood supply or arises from thoracic aorta