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23 Cards in this Set

  • Front
  • Back

Atresia? Fistula?

Atresia: closing of lumen




Fistula: opening of lumen

Esophageal atresia


with or without


tracheoesophageal fistulas (TEF's)

Failure in partitioning esophagus and trachea
~tracheoesophageal septum.


Baby looks normal until you feed the baby!!
Baby will vomit

Failure in partitioning esophagus and trachea


~tracheoesophageal septum.




Baby looks normal until you feed the baby!!


Baby will vomit

Polyhydromnios

Too much fluid in amniotic cavity; detected before birth. Indicates blockage along GI tract which includes esophageal atresia/TEF


Baby has to drink this amniotic fluid all the time to stimulate the GI development AND to digest fluid. If there is a blockage like esophageal atresia, baby will not drink the amniotic fluid and we see accumulation in amniotic cavity

H type TEF

Looks like H


Esophagus is continuous with trachea and bronchi

Looks like H




Esophagus is continuous with trachea and bronchi



VACTERL association

Vertebral anomalies


Anal atresia


Cardiac defects


Tracheoesophageal fistula (TEF's)


Esophageal atresia


Renal anomalies


Limb defects


*3 or more, dx'd with "VACTERL association"

Epithelium of internal lining of trachea, bronchi, lungs, and larynx is entirely made of?

endoderm (foregut origin)

Cartilaginous, muscular, and connective tissue components of trachea, bronchi, lungs is derived from?

splanchnic mesoderm surrounding foregut

visceral pleura and parietal pleura are derived from?

visceral pleura and parietal pleura are derived from?

visceral pleura - splanchnic mesoderm


parietal pleura - somatic mesoderm

Pericardioperitoneal canals


Lungs grow caudally in these spaces and then cease from the limit to abdomen



"Lung spaces"


"Lung spaces": Lungs grow caudally in these spaces and then cease from the limit to abdomen


Communication between thorax and abdomen

Pleuropericardial folds

Heart and lung separates when these folds fuse

Heart and lung separates when these folds fuse



Pleuroperitoneal folds

Fuses with septum transversum (primitive diaphragm) to separate thorax from abdomen

Fuses with septum transversum (primitive diaphragm) to separate thorax from abdomen

Congenital Diaphragmatic Hernia

Failure of pleuroperitoneal folds fusing with septum transversum, causing a latch opening in baby's diaphragm due to the absence of a pleuroperitoneal membrane. GI moves upwards into the chest cavity usually on the posterior LEFT side of diaphragm...

Failure of pleuroperitoneal folds fusing with septum transversum, causing a latch opening in baby's diaphragm due to the absence of a pleuroperitoneal membrane. GI moves upwards into the chest cavity usually on the posterior LEFT side of diaphragm


Result: Pulmonary Hypoplasia

Pulmonary Hypoplasia

Pressure on lungs and heart leading to underdeveloped lungs


baby dies

Pressure on lungs and heart leading to underdeveloped lungs




baby dies

Formation of diaphragm

1. septum transversum
2. pleuroperitoneal (fuses with septum transversum)
3. dorsal mesentery of esophagus
4. C3 C4 C5 somites/ voluntary skeletal muscle
**phrenic nerves motor diaphragm!

1. septum transversum


2. pleuroperitoneal (fuses with septum transversum)


3. dorsal mesentery of esophagus


4. C3 C4 C5 somites/ voluntary skeletal muscle


**phrenic nerves motor diaphragm!

1. Pseudoglandular period

Week 5 to 16


branching continues


no bronchioles


no alveoli

2. Canalicular period

Week 16 - 26


simple cuboidal epithelia


terminal bronchioles dividing into 2 or more, then into 3-6 alveolar ducts

3. Terminal sac period

Week 26 to birth


cuboidal bronchioles --> thin flat cells


blood/ lymph capillaries enter the terminal sacs creating primitive alveoli




respiration possible!!




Type 2 pneumocytes secrete surfactant

Surfactant

prevents lungs from collapsing


reduces surface tension


increases even more 2 weeks prior to birth




steroids/ glucocorticoids can stimulate pneumocytes II to produce surfactant

4. Alveolar period

month 8- childhood


number of terminal sacs steadily increasing


Type 1 pneumocytes becoming thinner to allow capillaries/blood to come into alveolar sacs creating a blood-air barrier between epithelial and endothelial sacs


mature alveoli not present before birth


lungs are fluid filled

post birth of lung maturation

1. alveoli increase in size in first 10 years


2. bronchioles and alveoli number increasing


3. lung growth


4. majority alveoli formed post-birth


5. continuous formation of primitive alveoli via capillaries into alveolar sacs

Respiratory distress syndrome

Premature babies; 20% deaths among newborns
Not enough surfactant
Alveoli collapsed; baby cannot breathe


Treatment: 
1. artificial surfactant
2. glucocorticoid produces surfactant; stimulates pneumocytes 2 to produce it

Premature babies; 20% deaths among newborns


Not enough surfactant


Alveoli collapsed; baby cannot breathe




Treatment:


1. artificial surfactant


2. glucocorticoid produces surfactant; stimulates pneumocytes 2 to produce it

Pulmonary agenesis

unilateral: absence of ONE lung, or lobe, or bronchi. usually associated with a cardiac defect or other condition 60% chance


compatible w life




bilateral: baby will die

Congenital cysts

cyst at terminal bronchi


cyst- honeycomb appearance


develop chronic infection