Embryology Flashcards

1
Q
  1. What structure arises from the primitive pharynx?
  2. What structure arises from the structure in the first question?
  3. What germ layers are these derived from?
A
  1. larnygotracheal groove gives rise to…
  2. laryngotracheal diverticulum (lung bud)
  3. endoderm
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

What parts of the respiratory tract arise from endoderm?

A

pulmonary epithelium

glands of larynx, trachea, bronchi

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

What region of the mesoderm are respiratory components derived from?

A

lateral plate mesoderm

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

The lateral plate mesoderm splits to give rise to..

A

splanchic mesoderm

somatic mesoderm

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

What is the visceral pleura derived from?

A

splanchnic mesoderm

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

What is the CT, smooth muscle, and cartilage of the respiratory tract derived from?

A

splanchnic mesoderm

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

what is the parietal pleura derived from?

A

somatic mesoderm

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

What is the role of the tracheoesophageal septum?

A

divides the trachea and esophagus at the origin point of the laryngotracheal diverticulum

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

What is the mechanism of error in the division of the tracheoesophageal septum?

A

decreased proliferation of endoderm

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

What is esophageal atresia? symptoms?

A

a blind esophagus due to errors in the tracheoesophageal septum

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

What is a tracheoesopheal fistula?

A

an abnormal connection between the trachea and esophagus, usually accompanied by esophageal atresia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

What secondary condition arises from tracheoesophageal fistulas? why does this occur?

A

polyhydramnios (excess amniotic fluid)
normally the amniotic fluid is ingested and transferred to the placenta, but the fetus is unable to ingest anything so the fluid builds up

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

When do the primary bronchi form off of the respiratory bud? what direction do they grow?

A

week 4

grow caudal/ventral

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

when do the primary bronchi split to become secondary (lobular bronchi)?

A

week 5

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

when do the secondary bronchi split to become tertiary?

A

week 7

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

when are the bronchopulmonary segments done branching and how many orders of branching occur?

A

week 24

17 orders of branching, 7 more after birth

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

When is the psudeoglandular stage of development?

A

weeks 5-17

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

what occurs in the pseudo-glandular stage of development? can the fetus survive at this stage?

A

endodermal tubes –> terminal bronchioles
(looks like exocrine glands)
not compatible with life

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
19
Q

when is the canalicular stage?

A

weeks 16-25

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
20
Q

what occurs in the canalicular stage? can it surive?

A

terminal bronchioles –> respiratory bronchioles –> alveolar ducts (primordial alveolar sacs)
maybe able to survive

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
21
Q

when is the terminal sac stage?

A

Week 24-birth

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
22
Q

what occurs during the terminal sac stage?

A

alveolar ducts –> alveolar sacs
alveoli form as epithelium thins
type I and II pneumocytes form
gas exhange can occur

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
23
Q

when is the alveolar stage?

A

week 32-age 8

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
24
Q

what occurs in the alveolar stage?

A

terminal sacs –> adult alveoli

primitive alveoli form and continues till age 9

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
25
Q

what cells produce surfactant and what is its role?

A

type II, reduces surface tension and prevents collapse of small alveoli

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
26
Q

what splits to form the intraembryonic coelem?

A
lateral plate mesoderm
forms somatic (dorsal) and splanchic mesoderm (ventral) with cavity in between
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
27
Q

How is are the two intraembryonic coelem brought together to form one big cavity?

A

lateral folding

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
28
Q

what is the arrangement of structures in the intraembryonic cavity after folding?

A

inside of body wall covered by parietal peritoneum
gut tube is covered in visceral peritoneum and suspended by dorsal mesesentary

note: remember lungs butt out from the gut tube at the layrngotracheal groove and grow into this cavity thats formed

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
29
Q

What moves the pericardial ceolum and septum transversum ventrally?

A

head ventral folding, brain grows over and pushes structures downward

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
30
Q

What are the parts of the intraembryonic ceolum after folding and where are they located?

A

pericardial coelum-ventral to heart tube, cranial to septum transversum
pericardioperitoneal canal=two tubes running along the ventral portion of the fetus connected to the pericardial coelum

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
31
Q

what does the pericardial-peritoneal canal become?

A

pleural cavities, peritoneal cavities

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
32
Q

what separates the pericardial cavity from the pericardial-peritoneal canal?

A

the pleuropericardial folds

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
33
Q

how do the pleuropericardial folds seperate the pericadial cavity from the pericardial-peroneal canal?

A

it grows medially from the somatopluera and becomes a pleuropericardial membrane separating the two cavities

lungs then grow ventrally and carve out the rest of the cavity

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
34
Q

what does the pleuropericardial membrane become?

A

fibrous pericardium

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
35
Q

What affect does oligohydraminos have on lung development?

A

decreases hydraulic pressure on developing lungs
impairs stretch receptors and lung growth

results in pulmonary hypoplasia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
36
Q

what causes respiratory distress syndrome? what are some buzzwords to narrow this down?

A

shitty type II pneumocytes that makes them incapable of producing surfactant

rapid labored breathing shortly after birth
“glassy membrane lungs”
“hyaline membrane lungs”

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
37
Q

What causes a congenital lung cyst?

A

dilation of terminal bronchioles with air or fluid

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
38
Q

what is pulmonary agenesis and what causes?

A

absence of lung growth

respiratory bud fails to split

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
39
Q

How do the pericardioperitoneal canals close?

A

pleuroparietal membrane grows ventrally and fuses with septum transversum

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
40
Q

At what week do we see definitive pleural and peritoneal cavities?

A

week 7

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
41
Q

what are the components of the diaphragm?

A

septum transversum (central tendon)

pleuroperitoneal membranes

musuclar ingrowth from body walls

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
42
Q

what issues arise from pericardioperitoneal canal closure?

A

congenital diaphragmatic hernia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
43
Q

what side do congenital diaphragmatic hernias usually occur?

A

left side, visceral bulge into pleural cavity

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
44
Q

what is an angioma?

A

bening growth of blood vessels and lymphatic capillaries

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
45
Q

What germ layer gives rise to early cardiogenic precursors?

A

splanchnic mesoderm –> angiogenic clusters (endothelial precursor cells) –> endocardial tubes and pre cardiomyocytes

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
46
Q

What structures arise from the primary heart field?

A

R/L atria, L ventricle

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
47
Q

What structures arise from the secondary heart field?

A

R ventricle, outflow tract

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
48
Q

What causes the two heart tubes to fuse together at midline to become one cardiac tubes?

A

lateral folding

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
49
Q

What are the three layers of the single heart tube and what do they arise from?

A

Endocardium from endothelial precursor cells
cardiac jelly= Splanchnic mesoderm
myocardium from precardiomyocytes

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
50
Q

What degenerates giving rise to the transverse sinus?

A

dorsal mesocardium

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
51
Q

what gives rise to the epicardium

A

proepicardial organ (From splanchnic)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
52
Q

How does the heart get from the cranial end and what is its position after this event?

A

cranial folding

it is cranial to the septum transversum, suspended in the body cavity via the dorsal mesocardium

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
53
Q

How is the primitive heart tube attached after folding?

A

outflow tract attached cranially, inflow tract attached caudally

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
54
Q

when does cardiac looping occur?

A

week 4

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
55
Q

Explain cardiac looping, why does this occur?

A

continued growth of the heart tube, but since its fixed at its cephalic and caudal ends, it folds and loops, moving the primordial ventricles to ventrally and to the right

56
Q

what role does the secondary heart field play in cardiac looping?

A

these cells are inhibited by the notocord until lateral folding occurs, then secretes growth factors that contribute to the lengthening of the tube

57
Q

What are the definitive regions of the early heart after cardiac looping?

A

superior region connected to venous sinus will become atria

inferior region connected to outflow tract will become ventricles

58
Q

What is the path of oxygenated blood in fetal circulation?

A

umbilical vein –> ductus venosus –> right atrium –> foramen ovale –> left atrium –> left ventricle –> aorta
(some mixing occurs in right ventricle)

59
Q

What is the path of deoxygenated blood in fetal circulation?

A

SVC –> RA (some mixing with oxygenated)–> right ventricle –> pulmonary trunk –> ductus arteriosus (bypasses pulmonary circulation –> descending aorta –> out

60
Q

What is dextrocardia? what is the cause?

A

reversal of ventricles

errors in cardiac looping

61
Q

What is situs invertus?

A

total reversal of all internal organs

62
Q

What is situs ambiguous?

A

partial reversal of internal organs

63
Q

What is visceroatrial heterotaxia?

A

a type of situs ambiguous where the heart is on the right and GI is normal

64
Q

Describe the primitive venous inflow into the sinus venosus

A

3 bilaterally symmetrical veins
R/L vitelline
R/L umbilical
A/P cardinal

65
Q

How is the primitive venous inflow remodeled so all venous return goes to right atrium?

A

left to right shunting

66
Q

What is the fate of the R and L vitelline veins?

A

right becomes hepatic portal system

left regresses

67
Q

What is the fight of the R and L umbillical veins?

A

Right-regresses and becomes r umbilical ligament

Left-proximal part regresses, distal connects to ligamentum teres hepatis

68
Q

What is the fate of the anterior cardinal veins?

A

left to right shunting forms a branchiocephalic anastomosis and later remodeling to become the SVC on the right

69
Q

What is the fate of the posterior cardinal veins?

A

Supracardinal and subcardinal veins add on
left to right shunting turns them into the IVC
also supracardinal becomes azygos and hemiazygos i guess

70
Q

What features arise when sinus venosum is incorporated into the wall of the R atrium?

A

crista terminalis
right horn of sinus venosus=smooth part of right atrium
left horn of sinus venosus=coronary sinus

71
Q

What is the crista terminalis?

A

interior of the atrial wall that separates the smooth and rough parts

72
Q

WHAT IS THE SINUS VENARUM?!?!?

A

smooth part of right atria formed from right horn of sinus venosus

73
Q

What two processes result in cardia septa formation?

A
  1. endocardial cushion formation (contributes to membranous part)
  2. differential growth (muscular growth of septum)
74
Q

Where does endocardial cushion tissue come from?

A

outgrowth of endocardium

75
Q

what part of the septa does endocardial cushion contribute to?

A

membranous inter-ventricular septum and atrial septum

76
Q

How is the AV septum formed? How does this lead to formation of AV canals? are neural crest cells involved in this process?

A

endocardial cushion tissue grows from ventral and dorsal sides and meet in middle

lateral parts dont fuse and are the AV canals

NO NCC

77
Q

What closes off the outflow tract?

A

conotruncal endocardial cushion AND NCC

78
Q

What occurs in a persistent AV canal? cause? symptoms? what is it commonly associated with?

A

failure of endocardial cushion cells
results in an ASD and VSD
sx: pulmonary HTN, intolerance to exercise, SOB, cardiac congestion

downs syndrome

79
Q

Describe how the atria are divided (sorta long but deal with it)

A
  1. Septum Primum and dorsal mesenchymal protrusion grows from dorsal to ventral towards endocardial cushion, hole in it is foramen primum
  2. Foramen primum closes, foramen secundum opens
  3. Septum secundum develops and covers most of the foramen secundum
  4. Remaining opening for foramen secundum is now foramen ovale
80
Q

What keeps foramen ovale open during fetal times?

A

greater pressure in RA vs LA because pulmonary circulation doesn’t exist yet

81
Q

What congenital abnormalities result in cyanosis? (5 Ts

A
  1. truncus arteriousis (persistant)
  2. transposition of great vessels
  3. tricuspid atresia
  4. tetrology of fallot
  5. TAPVR

VSD>ASD>PDA

82
Q

What causes cyanosis? what would cause early cyanosis vs late?

A

lack of oxygenated blood
mixing of oxygenated and deoxygenated blood
early=right to left
later=left to right

83
Q

How does the foramen ovale close at birth?

A
  1. Infant takes breath (when born)
  2. Everything opens and pulmonary vascular resistance
    decreases
  3. Pressure in right atrial pressure drops compared to left
  4. Higher LA pressure forces septum primum against
    septum secundum and they fuse
  5. Fossa ovalis remains
84
Q

What causes a patent foramen ovale? is this usually treated? what complications can arise from this down the road?

A

septum primum and septum secundum fail to fuse at birth

no, but later on thromboemboli that enter atrial circulation can go from RA to LA then to brain

85
Q

By what 3 ways can an atrial septal defect occur? how is this different from a patent forament ovale?

A
  1. failure of development of septum secundum
  2. excessive absorption of septum primum
  3. patent foramen primum

in this septa fail to develop in PDA the are there but fail to fuse

86
Q

What do the septum primum and secundum arise from?

A

atrial wall and AV cushion

87
Q

How do the developing ventricles gain access to the AV canal?

A

truncus arteriosis shifts right
cardiac cushion cells shift left
this shifts the right AV canal over

88
Q

What is a double outlet right ventricle? how does this occur? symptoms? will this person have a VSD?

A

insufficent shifting of the truncus arteriosis
both aorta and pulmonary artery are in right ventricle
yes to VSD
sx: cyanosis, breathlessness

89
Q

How is the outflow tract become the aorta and pulmonary trunk?

A
  1. NCC migrate to truncus arteriosus (undivided outflow
    tract) and conus cordis, and combine with conotruncal endocardial cushion cells
  2. Transform into mesenchyme that make two conotruncal ridges
  3. These two ridges grow towards each other and zip and
    spiral
  4. Aortopulmonary septum made and fuses with interventricular septum
  5. Eventually becomes ascending aorta and pulmonary
    trunk
90
Q

What are the three major tissue structures needed to separate the left and right ventricle? where do they come from

A
  1. muscular interventriclar septum from outgrowth
  2. aorticopulmonary septum rotates and fuses with muscular interventricular septum to form membranous part
  3. endocardial cushion cells contribute to membranous part of IVS
91
Q

What is usually the cause of the major outflow tract defects? what is associated with all of them?

A

Defects in migration of neural crest cells, a VSD

92
Q

What is persistent truncus arteriousus? cause? VSD?

A

failure of aorta and pulmonary trunk to fully divide

failure of NCC, has a VSD

93
Q

What occurs in transposition of great vessels? cause? what do they need in order to survive?

A

great vessels switched, aorta in right ventricle, pulmonary trunk in left ventricle (2 closed loops, no oxygenated blood to system)

caused by shitty NCC and no spiraling

need a shunt to survive, VSD, patent ductus arteriousis or patent foramen ovale

94
Q

What occurs in tetrolagy of fallot? (PROV) cayse?

A
pulmonary stenosis (yuge giveaway)
RV hypertrophy (Cause of the pulmonary stenosis)
overriding aorta (aorta over VSD)
VSD

cause: shit NCC resulting in misplacement of the infundibular septum

95
Q

What is pulmonary valvular atresia? signs? what do they need to survive?

A

no pulmonary semilunar valve
results in right ventricular hypoplasia
need PFO (so deoxygenated blood can get from right to left) , PDA (so deoxygenated blood can enter pulmonary circulation) to live

96
Q

What is aortic valve atresia? signs? what do they need to survive?

A

no aortic valve, LV hypoplasia
need atrial septal defect (so oxygenated blood can go from left to right) and patent ductus arteriosis
(so blood can get into aorta)

97
Q

what occurs in a bicuspid aortic valve?

A

2 leaflets instead of 3

LV hypertrophy cause it creates more resistance

98
Q

What occurs in tricuspid atresia? what occurs? what do you need in order to survive?

A

no tricuspid valve
RV hypoplasia
need ASD, VSD or you die

99
Q

What occurs in a hypoplastic left ventricle? what do you need to survive and why?

A

underdeveloped LV resulting in shit aortic semilunar and mitral valves resulting in shit ascending aorta

VSD
-so that oxygenated blood can move thr, and patent

foramen ovale or ASD,
-to get oxygenated blood from left to right side of heart

PDA
-so blood van go from pulmonary circulation to systemic

100
Q

Which aortic arches contribute to nothing and just regress?

101
Q

which aortic arches contribute the most?

A

III, IV, VI

102
Q

What is the fate of the cervical segmental arteries?

A

vertebral a.

103
Q

what is the fate of the left 7th intersegmental artery?

A

left subclavian a

104
Q

what is the fate of the thoracic segmental arteries?

A

internal thoracic aa.

105
Q

What is the fate of aortic arches I

106
Q

what is the fate of aortic arches II

107
Q

what is the fate of aortic arch III on the right

A

R: R common carotid, distal portion is internal carotid, proximal is external carotid

108
Q

what is the fate of the left aortic arch III

A

becomes left common carotid, proximal is external distal is internal

109
Q

What is the fate of left aortic arch IV?

A

ascending aorta, aortic arch, descending aorta

110
Q

what is the fate of right aortic arch IV?

A

right subclavian a.

111
Q

what is the fate of aortic arch V on both sides?

112
Q

what is the fate of aortic arch VI on the right?

A

proximal becomes right pulmonary a.

distal regresses

113
Q

what is the fate of the aortic arch VI on the left?

A

proximal becomes left pulmonary a.

distal becomes ductus arteriosus

114
Q

Why does the recurrent laryngeal nerve rise from the vagus nerve at two different levels in the adult?

A

on the right side the distal portion of VI regresses and it gets pulled up and caugh under the brachiocephalic trunk

on the left side it gets caught on the ligamentum arteriousus

115
Q

what is the purpose of the ductus arteriousus?

A

to augment flow of oxygenated blood from pulmonary to systemic circulation in a fetus

116
Q

how does the ductus arteriosus close after birth?

A

changes in O2 tension and blood flow decrease prostaglandin levels spurring smooth muscle contraction and it closes

117
Q

what occurs in patent ductus arteriousus? what occurs to the heart as a result?

A

after birth, pulmonary circulation resistance drops dramatically

if this duct remains open, high pressure aortic circulation will take the path of least resistance into pulmonary circulation

left ventricular hypertrophy, pulmonary a congestion,

118
Q

what is coarction of the aorta and which type is better and why?

A

thinning of aorta pre or post ductus arteriousus

post ductal is better because collateral circulation through the internal thoracic and intercostal arteries allows for profusion of blood to lower limbs

119
Q

what causes abnormal origin of the right subclavian?

A

persistence of the right distal segment of dorsal aorta

regression of right proximal segment (IV)

R subclavian now wraps around espophagus, can cause dysphagia

120
Q

what causes double aortic arches? what does this do

A

persistence of right distal segmant of dorsal aorta (VI)

entraps esophagus and trachea

121
Q

what causes right aortic arch?

A

persistence of right distal segment

regression of left distal segment

122
Q

what causes interrupted aortic arch? how does blood supply get to the descending aorta?

A

-abnormal regression of right and left arch IV
-ascending part is fine
descending part is toast

need patent ductus arteriosus to connect pulmonary trunk to descending aorta

123
Q

How does double SVC occur?

A
no brachiocephalic anastomosis forms
no brachiocephalic vein
two SVC
right is normal
left drains to oblique sinus
124
Q

how do you get a left sided SVC?

A

brachiocephalic anastomosis shunts blood right to left instead of left to right

connects to right atrium via oblique sinus

125
Q

what does the truncus arteriosis become?

A

ascending aorta and pulmonary trunk

126
Q

what does the bublus cordis become?

A

smooth part of outflow tract of ventricles

127
Q

what does endocardial cushion become?

A

Atrial septum, membranous ventricular septum, AV and semilunar valves

128
Q

what does the left horn of the sinus venosus become?

A

coronary sinus

129
Q

what does the right horn of the sinus venosus become?

A

smooth part of right atrium (Sinus venarum)

130
Q

what does the right common and anterior cardinal vein become?

131
Q

What congenital abnormalities are associated with rubella?

A

PDA, pulmonary artery stenosis, septal defects

132
Q

What congenital abnormalities are associated with downs?

A

AV septal defect (endocardial cushion( VSD, ASD

133
Q

what congenital abnormalities are associated with turner syndrome

A

coarction of the aorta

134
Q

What does the conus arteriosus form from?

A

Bulbus cordis

135
Q

What is the most common ASD?

A

Septum secundum perforation.

136
Q

How do you keep open a ductus arteriosus in hte case of heart defect

A

Ductus arteriosis usually closes within 1-2 hours of birth
Closes because of smooth muscle contraction of tunica media
Before birth there is low oxygen content = high prostaglandins –> which keep the smooth muscle of the artery relaxed and open. Flow of O2 at birth causes inhibition of prostaglandins → the smooth muscle to contarct.