Respiratory System Flashcards

1
Q

What is the lower respiratory system

A

Larynx, trachea, bronchi, and lungs

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2
Q

When does the lower respiratory system begin to develop

A

4th week

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3
Q

The respiratory system starts as a median outgrowth-the ___ ___-that appears in the floor of the caudal end of the primordial pharynx

A

Laryngotracheal groove

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4
Q

The primordium of the tracheobronchial tree develops ___ to the __ pair of pharyngeal pouches

A

Caudal

Fourth

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5
Q

What does the endodermal lining of the laryngotracheal groove give rise to

A

Pulmonary epithelium and glands of the larynx, trachea, and bronchi

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6
Q

What does the splanchnic mesoderm surrounding the foregut make

A

CT, cartilage, smooth muscle

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7
Q

Signaling pathways of __, __, and ___ control patterning of the expression of __ and __ in the early foregut for the differentiation of the trachea from the esophagus.

A

BMP, Wnt, and FGF

Sox2 and NKx2.1in

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8
Q

In ventral areas, __ is activated while _ is suppressed

A

Nkx2.1

Sox2

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9
Q

By the end of the 4th week, the laryngotracheal groove has evaginated to form a pouch like ___ ____, which is located ventral to the caudal part of the foregut

A

Laryngotracheal diverticulum

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10
Q

As the diverticulum elongates, its distal end enlarges to form a globular ___ ___

A

Respiratory bud

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11
Q

The laryngotracheal diverticulum soon separates from the __ __, but it maintains communication with it through the ___ ___ ___

A

Primordial pharynx

Primordial laryngeal inlet

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12
Q

As hte diverticulum elongates, it is invested with __ ___

A

Splanchnic mesoderm

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13
Q

Longitudinal tracheoesophageal folds develop in the laryngotracheal diverticulum, approach each other, and duse to form a partition - the ___ ____

A

Tracheoesophageal septum

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14
Q

The tracheoesophageal septum divides the cranial part of the foregut into a ventral part, the ___ ___ and a dorsal part, the ___

A

Laryngotracheal tube(primordium of the Arnce , trachea, bronchi, and lungs

Primordium of the oropharynx and esophagus

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15
Q

The opening of the laryngotracheal tube into the pharynx becomes the ___ ___ __

A

Primordial laryngeal inlet

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16
Q

The epithelial lining of the larynx develops from the ___ of the cranial end of the laryngotracheal tube

A

Endoderm

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17
Q

The cartilages of the larynx develop from cell populations int he __ and __ pairs of pharyngeal arches

A

4 and 6

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18
Q

The laryngeal cartilages develop from the mesenchyme that is derived from ___

A

Ncc

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19
Q

The mesenchyme at the cranial end of the laryngotracheal tube proliferates rapidly, producing paired __ ___

A

Arytenoid swellings

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20
Q

These swellings grow toward the tongue, converting the __ __ into a t shaped ___ ___

A

Primordial glottis

Laryngeal inlet

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21
Q

The laryngeal epithelium proliferates rapidly, resulting in temporary occlusion of the laryngeal lumen.

A

Ok

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22
Q

Recanalization of the larynx occurs by the __ week

A

10

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23
Q

The laryngeal ventricles form during their recanalization process. These recesses are bound by folds of mucous membrane that evolve into the __ __ and ___ ___

A

Vocal folds(cords) and vestibularfolds

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24
Q

The ___ develops from the caudal part of the hypopharyngeal eminence, a prominence produced by the proliferation of the mesenchyme in the ventral ends of the third and fourth pharyngeal arches

A

Epiglottis

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25
Q

The rostral part of the eminence forms the posterior third of pharyngeal part of the tongue

A

Ok

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26
Q

The laryngeal muscles develop from ___ in the __ and __ pairs of pharyngeal arches and are therefore innervated by what

A

Myoblasts 4 and 6

Laryngeal branches of the vagus nerves t

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27
Q

Growth of the larynx and epiglottis is rapid during the firs __ years after birth, by which time the epiglottis has reached its adult form and position

A

3

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28
Q

Laryngeal atresia

A

Rare

Obstruction of the upper fetal airway bc of congenital high airway obstruction syndrome

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29
Q

In laryngeal atresia, distal to the atresia or stenosis, the airway becomes ___, the lungs are ____, the diaphragm is ___ or ____ and _____ or ____ is present

A

Dilated
Hyperplastic
Flattened or inverted
Fetal hydrops or ascites

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30
Q

How diagnose laryngeal atresia

A

Prenatal ultrasound

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31
Q

The endodermal lining of the laryngotracheal tube distal to the larynx differentiates into the epithelium of ___ of the trachea and ____ epithelium

A

Glands

Pulmonary

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32
Q

The cartilage, CT, and muscles of the trachea are derived from the ___ ___ surrounding the laryngotracheal tube

A

Splanchnic mesoderm

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33
Q

Tracheoesophageal fistula

A

Abnormal passage between the trachea and esophagus
1/3000
Males

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34
Q

In most cases TEF is associated with __ __

A

Esophageal atresia

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35
Q

TEF results from incomplete division of the cranial part of the foregut into the ___ and ____ parts during the __ week

A

Respiratory
Esophageal
4th

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36
Q

Incomplete fusion of the tracheoesophageal folds result in a defecting ___ __ and communication between the trachea and esophagus

A

Tracheoesophageal septum

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37
Q

__ is the most common anomaly of the lower respiratory tract

A

TEF

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38
Q

Esophageal atresia

A

Blind ending of the superior part of the esophagus

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39
Q

Usual TEF

A

Esophageal atresia and a joining of the inferior part to the trachea near its bifurcation

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40
Q

Infants with usual TEF

A

Cough and choke when swallowing
Regurgitate milk
Gastric reflux into trachea and lungs

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41
Q

___ is often associated with esophageal atresia

A

Polyhydramnios

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42
Q

Why polyhydramnios with esophageal atresia

A

Excess amniotic fluid accumulates bc fluid cant pass to the stomach and intestines for absorption and subsequent transfer through the placenta to the maternal blood for disposal

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43
Q

Stenosis and atresia of the trachea are uncommon and associated with __

A

TEF

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44
Q

What causes stenosis and atresia of the trachea

A

Partitioning of the foregut into he esophagus and trachea

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45
Q

Incomplete tracheal atresia

A

A web of tissue obstructs airflow

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46
Q

The respiratory bud develops at the caudal end of the ___ ___ during the __ week

A

Laryngotracheal diverticulum

4th

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47
Q

The respiratory bud don divides into two outpouchings-__ __ __

A

Primary bronchial buds

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48
Q

Later, __ and ___ bronchial buds form and grow laterally into the pericardioperitoneal canals

A

Secondary and tertiary

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49
Q

Together with the surrounding splanchnic mesoderm, the bronchial buds differentiate into the __ and their ramifications in the lungs

A

Bronchi

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50
Q

Early in he __ week the Connection of each bronchial bud with the trachea enlarges to form the primordia of main bronchi

A

4

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51
Q

The main bronchi subdivide into secondary bronchi that form __, ___ and ____ branches

A

Lobar
Segmental
Intrasegmental

52
Q

On the right, the superior secondary bronchus supplies the upper lobe of the lung, whereas the inferior secondary bronchus subdivides I tot he bronchi, one connecting to the middle lobe of the right lung and the other connecting to the lower lobe

A

On the left the two secondary bronchi supply the upper and lower lobes of th Leung,. Each secondary bronchus undergoes progressive branching

53
Q

How many segmental bronchi are there int he right and left and when do they begin to form

A

10 right
8-9 left
7th week

54
Q

As the segmental bronchi form, the surrounding __ also divides

A

Mesenchyme

55
Q

Each segmental bronchus, with its surrounding mass of mesenchyme, is the primordium of a ___ ___

A

Bronchopulmonary segment

56
Q

By 24 weeks, approcimately ___ orders of branching have occurred and respiratory bronchioles have developed

A

17

57
Q

An additional __ orders of airways develop after birth

A

7

58
Q

As the bronchi develop,, cartilaginous plates are formed from the surrounding ___ ___

A

Splanchnic mesoderm

59
Q

The bronchial smooth muscle nd CT and the pulmonary CT and capillaries are also derived from the ___

A

Mesenchyme

60
Q

As the lungs develop, they acquire a layer of ___ __ from the ___ ___

A

Visceral pleura

Splanchnic mesoderm

61
Q

With expansion, the lungs and pleural cavities grow caudally into the mesenchyme of the body wall and soon lie close to the ___

A

Heart

62
Q

The thoracic body wall becomes lined by a layer of ___ ___ derived from the __ ___

A

Parietal pleura

Somatic mesoderm

63
Q

The space between the visceral and parietal pleura is the ___ ___

A

Pleural cavity

64
Q

What are the four stages of lung maturation

A

Pseudoglandular
Canalicular
Terminal saccular
Alveolar

65
Q

When is the pseudoglandular period

A

5-17 weeks

66
Q

During the pseudoglandular phase, the developing lungs resemble an _____ ____

A

Exocrine gland

67
Q

By 16 weeks, all of the major elements of the lung have primed, except what

A

Those involved with gas exchange

68
Q

What happens if a fetus is born during the pseudoglandular phase

A

Die cant breathe respiratoion is not possible

69
Q

When is the canalicular period

A

16-25 weeks

70
Q

Why does the canalicular period overlap the pseudoglandular phase

A

Cranial segments of the lungs mature faster than caudal segments

71
Q

In the canalicular period, the lumina of the bronchi and the terminal bronchioles become ___ and the lung tissue becomes __ ___

A

Larger

Highly vascular

72
Q

By 24 weeks, each terminal bronchiole has given rise to two or more __ ___, each of which then divides into three to six tubular passages-___ ___ ___

A

Respiratory bronchioles

Primordial alveolar ducts

73
Q

Respiratorion is possible toward the end of the canalicular stage because Moe thin walled __ ___ have developed at the ends of the respiratory bronchioles and the lung tissue is well vascularized

A

Terminal sacs

74
Q

What happens if a fetus is born 24-26 weeks

A

May survive if given intensive care, it often dies because its respiratory and other systems are relatively immature

75
Q

Terminal saccular period. When

A

24 weeks until late fetal period

76
Q

During the terminal saccular period, many more __ ___ develop an their epithelium becomes very ___

A
Terminal sacs (primordial alveoli 
Thin
77
Q

In their terminal saccular period, capillaries begin to bulge into these space. The intimate contact between epithelial and endothelial cells, establish the __ ___ ___, which permits adequate gas exchange for survival

A

Blood-air barrier

78
Q

The 26 weeks, the terminal sacs ar lined mainly by squamous epithelial cells of the endodermal origin-___ __ ___-across which gas exchange occurs

A

Type I pneumocytes

79
Q

Int he remains saccular period, the capillary networks proliferates rapidly in the mesenchyme around the developing alveoli, and there is concurrent active development of __ ___

A

Lymphatic capillaries

80
Q

In their terminal sac period, scattered among the squamous epithelial cellls are rounded secretory epithelial cells-__ _ ___, which secrete __ ___,

A

Type II pneumocytes

Pulmonary surfactant

81
Q

What is surfactant

A

Complex mixture of phospholipids and proteins

82
Q

Surfactant forms a monomolecular film over the interior walls of the alveolar sacs and counteracts surface tension forces at the air-alveolar interface. This facilitates ___ of the terminal sacs

A

Expansion

83
Q

The maturation of alveolar type II cells and the production of surfactant vary widely in fetish’s of different ages. When does surfactant production begin

A

20-22 weeks

84
Q

But surfactant does not reach adequate levels until when

A

Late fetal period

85
Q

When babies are born during the terminalsaccular period, both increased surfactant production , induced by antenatal corticosteroids, and ___ ___ __ ___ have increased the rates of survival of these infants

A

Postnatal surfactant replacement therapy

86
Q

When is the alveolar period

A

Late fetal period to 8 years

87
Q

At the beginning of the alveolar period, each respiratory bronchiole terminates in a cluster of thin walled terminal space that are separated from one another by loose ___

A

CT

88
Q

These terminal space represent future __ ___

A

Alveolar ducts

89
Q

The _____ ____ is sufficiently thin to allow gas exchange

A

Alveolocapillary membrane

90
Q

The transition from dependence ont he placenta for gas exchange to autonomous gas exchange after birth requires the following adaptive changes int he lungs

A

Production of surfactant int he alveolar space
Transformation of the lungs into gas exchanging organs
Establishment of parallel pulmonary and systemic circulations

91
Q

__% of mature alveoli mdevelop in the the post natal period

A

95

92
Q

Before birth, the primordial alveoli appear as small bulges on the walls of the respiratory bronchioles and alveolar sacs

A

After birth the primordial alveoli enlarge as the lungs expand, however most of the increase in the size of the lungs results from a continues increase in the size of the alveoli

93
Q

Alveolar development is largely complete by _ years of age, but new alveoli may be added until _ years

A

3

8

94
Q

Unlike mature alveoli, immature alveoli have the potential for forming additional primordial alveoli

A

Ok

95
Q

Approximately __ million primordial alveoli, one half the number in adults are present in the lungs of full term neonates

A

150

96
Q

On chest radiographs, the lungs on neonates appear __ than adults

A

Denser

97
Q

Between the 3rd and 8th years, the adult complement of __ million alveoli is achieved

A

300

98
Q

Three factors are essential for normal lung development

A

Adequate thoracic space for lung growth adequate amniotic fluid volume
Fetal breathing movements

99
Q

The mechanism modulating lung morphogenetic and formation of blood vessels int he lungs involved the transcription factors __ and ___ signaling

A

Sox17

Wnt

100
Q

Fetal breathing movement occur ___ birth, exerting sufficient force to cause aspiration of some amniotic fluid into the lungs

A

Before

101
Q

These fetal breathing movement soccur approximately 50% of the time and only during ___

A

REM sleep

102
Q

Fetal breathing movements stimulate lung development

A

By the time the fetus is born it has several moths of breathing exercise

103
Q

FETAL BREATHING MOVEMENTS INCREASE AS THE TIME OF DELIVERY APPROACHES

A

Ok

104
Q

At birth the lungs are ___ filled with fluid from the amniotic cavity, lungs and tracheal glands

A

Half

105
Q

How does aeration fothe lungs at birth occur

A

Rapid replacement of intralveolar fluid by air

106
Q

What are the three routes by which the lungs are cleared at birth

A

Through the mouth and nose by pressure on the thorax during vaginal delivery

Into the pulmonary capillaries and pulmonary arteries and veins

Into the lymphatic vessels

107
Q

Oligohydramnios

A

Insufficient amount of amniotic fluid

108
Q

When oligohydramnios is severe and chronic, lung development is ___

A

Restarded

109
Q

Why does oligohydramnios retard lung growth

A

Reduced hydraulic pressure int he lungs and its consequently effects on lung calcium regulation may result in pulmonary hypoplasia

110
Q

RDS effects _% of live newborns

A

2

111
Q

Who is most susceptible to rds

A

Premature babies

112
Q

Another name for rds

A

Hyaline membrane disease

113
Q

What is the major cause orf rds

A

Surfactant defiency

114
Q

Prolonged intrauterine ____ may produce irreversible changes in type II alveolar cells, making them incapable of producing surfactant

A

Asphyxia

115
Q

___ are potent stimulators of fetal surfactant production and may be given to the mother if early delivery is a risk

A

Corticosteroids

116
Q

Describe breathing of baby with rds

A

Rapid, labored breathing

117
Q

__% of all neonatal disease results from RDS or its complications

A

30

118
Q

The lungs are under inflated and the alveoli contain amorphous material (hyaline membrane) from substances int he circulation and the injured pulmonary epithelium in __

A

RDS

119
Q

Treatment for RDS

A

Supplementary oxygen and artificial surfactant -more than 90% of neonates with RDS survive

120
Q

Fresh healthy lungs always contain some air. Pulmonary tissue floats. In contract a diseased lung may __

A

Sink

121
Q

Do lungs of stillborn sink or float

A

Sink

122
Q

Congenital diaphragmatic hernia

A

Lungs may not envelop normally

123
Q

Why have lung hypoplasia with congenital diaphragmatic hernia

A

Changes in growth factors that exist before the abdominal viscera becomes abnormally positioned.

124
Q

Characterization of lung hypoplasia

A

Markedly reduced lung volume .

125
Q

Why di infants with congenital diaphragmanetic hernia die

A

Pulmonary insuffiency, despite optimal prenatal care, because their lungs are too hypoplastic to support extrauterine life