Developmental aspect of lung disease Flashcards

1
Q

Whats the gestational age for embryonic, Pseudoglandular, canalicular, saccular and alveolar?

A
E: 3-8 weeks
P: 5-17 weeks
C: 16-26 weeks
S: 24-38 weeks
A: 36 weeks
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2
Q

Describe the morphogenesis in embryonic

A

Lungs originate from oespophagus

Respiratory diverticulum – trachea

In stage C, the lobes can sometimes be seen developing

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3
Q

Describe the morphogenesis in pseudoglandular

A

COnducting segments start to develop alongside the cilia and mucous

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4
Q

Describe the morphogenesis in canalicular

A

Early gas exchange begins to start

Development of small sacs that develop into alveoli

Surfactant organs began to develop too

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5
Q

Describe the morphogenesis in saccular

A

Precursors for alveoli

Development of type 1 and type 2

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6
Q

Describe the morphogenesis in alveolar

A

Once filled with air will change shape and geometry and continue to grow for the next 2-3 years

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7
Q

What is postnatal lung growth?

A

Alveolar septation continues
100-150 million at birth to 200-600 million at 3-8 years
Increased alveolar dimensions thereafter
MRI suggests new alveolar development up to late childhood

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8
Q

At which week can babies survive with ventilation?

A

Week 24

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9
Q

Name 3 common congenital upper abnormalities

A

Tracheal agenesis and stendosis
tracheomalacia
tracheo-oesophageal fistula

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10
Q

Name 3 common congenital lower abnormalities

A

Lung agenesis/pulmonary hypoplasia
bronchogenic cyst
CPAM
congenital diaphragmatic hernia

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11
Q

When does ultrasound happen for mum and baby?

A

At around 12 weeks during antenatal screening

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12
Q

Presenting features in newborn for lung disease

A

Newborn
Tachypnoea
Respiratory distress
Feeding issues

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13
Q

Presenting features in Childhood for lung disease

A

Stridor/wheeze
Recurrent pneumonia
Cough
Feeding issues

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14
Q

Presenting features in asymptomatic for lung disease

A

Incidental findings

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15
Q

What is tracheal agenesis?

A

Very rare an presents at birth with acute respiratory distress and inability to intubate

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16
Q

What is tracheal stenosis?

A

Very rare
Complete tracheal cartilage rings, may be generalized or segmental
Present at birth or within first year

Funnel shape near the end of the branching into two bronchi

17
Q

What is tracheomalacia?

A

Dynamic abnormal collapse of tracheal walls
and leads to floppiness.

Can be caused by external compression

18
Q

What is presentation of tracheomalacia?

A
Presentation:
Barking cough
Recurrent “croup”
Breathless on exertion
Stridor/wheeze
19
Q

What is tracheo-oesphageal fistula?

A

Abnormal connection between trachea and oesphagus

Association with genetic conditions

20
Q

What is presentation and treatment of tracheo-oesphageal fistula?

A

May be diagnosed antenatally or postnatally

Presentation: 
Choking
Colour change
Cough with feeding
Unable to pass NG

Treatment with surgical repair

Complications include tracheomalacia, strictures, leak and reflux

21
Q

What is congenital pulmonary airway malformation?

A

Abnormal non-functioning lung tissue
80% detected antenatally
Occur sporadically

May resolve spontaneously in utero
Conservative management if asymptomatic
Surgical intervention may be required
Possible risk of malignant change

22
Q

When is diaphragm developed and closure occurs?

A

Around 7 weeks from multiple tissues

Closure by 18weeks

23
Q

Describe congenital diaphragmatic hernia and its managment

A

Affects 1 in 2500 births
Different types, most common Bochdalek (90%)
Usually left side > right side

Most diagnosed antenatally
Some cases diagnosis late

Management surgical repair

Prognosis depends on degree of lung hypoplasia

24
Q

What are the changes in lungs after birth?

A

Significant changes occur at birth after first breath

Lungs inflate and fluid in lungs is absorbed

25
Q

What is transpient trachypnoea?

A

Transient tachypnoea of newborn
Associated with C-section
Improves within 1-2 days

26
Q

What is the surfactant system made up from?

A

Surfactant
Complex mix of phospholipids and lipophilic proteins
Reduces surface tension at alveoli and promote gas exchange

Type II pneumocytes
Produce and secrete surfactant
Differentiate 24-34 weeks

27
Q

When does Respiratory distress sydnrome occur? RDS

A

Hyaline membrane disease

Occurs with preterm infants with surfactant deficiency

28
Q

Treatment for RDS?

A

Antenatal steroids
Surfactant replacement
Appropriate ventilation and nutrition

29
Q

What is chronic lung disease and treatment?

A

Ongoing oxygen requirement at term and multifactorial causes and associated with increased childhood respiratory morbidity.
May cause COPD in future

30
Q

What does remodelling in lungs involve?

A

Its caused by the interference of intercellular signalling.

Its the alteration of airway structure following external influence:
Environmental exposures
Chronic diseases of childhood
Infection

31
Q

Describe remodelling in asthma

A
Chronic inflammation
Increased bronchial responsiveness
Increase mucus secretion
Airway oedema
Airway narrowing
32
Q

Describe remodelling in chronic lung disease

A

Chronic inflammation
Interference inter-cellular signalling
Treatment toxicity

33
Q

What does smoking do on rate of decline in FEV?

A

Smoking decreases the FEV as age increases