Development of GI Flashcards

(78 cards)

1
Q

the 7th week, we see urorectal septum fusing with the clocal; then its divided into dorsal anal membranes and a larger ventral genital membrane

Fusion of the urorectal septum with the cloacal membrane becomes the perineum

A
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1
Q

Abnormalities of the Hindgut

A

Congenital Megacolon

1-neural crest cells do not migrate into the wall of the colon during the 5-7th weeks gestational age

2-results in a decrease in parasympathetic ganglion cells

3-decreases peristalsis in the aganglionic segement

4-we see an elargement in the proximal part of the colon

5-results in a lack of migration of neural crest cells into colon 5-7th week

1/5,000

**Most common cause of neonatal obstruction of the colon**

accounts for 33% of neonatal obstruction

  • males more affected than females with a 4:1 ratio
  • most cases, rectum and sigmoid colon are involved
  • obstruction is primarily due to lack of peristalsis in that part of the colon without ganglion cells
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2
Q

In the liver as it develops: initially the right and left lobe are of equal size, but then the right lobe becomes larger as hematopoisis begins during the 6th week of embryological development

A
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2
Q

What disorder presents with complete or partial bowel obstruction?

A

Annular Pancreas

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2
Q

What week does failure of the anal membrane to rupture result in an imperforate anus?

A

8th

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3
Q

where is the duodenum developed from?

A

caudal part of the foregut and the cranial part of the midgut

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3
Q

Pancreas

A

with rotation , the pancreatic buds fuse;

happens as a result of rotation

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4
Q

Patent Urachus, urachal sinus or urachal diverticulum

Hindgut abnormalities

A
  • Allantois runs along the umbilicus
  • Allantois gives rise to the urachus
  • Urachus is a canal that drains the bladder nd runs within the umbilical cord to the urinary bladder in the fetus
  • as the fetus develops, the canal (or tube), becomes obliterated; HOWEVER, in this situationm the tube does not become obliterated sp we have a patent urachus, urachal sinus, urachal diverticulum or cyst
  • incomplete obliteration of allantois may involve the umbilicus
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4
Q

Abnormalities if the Hindgut

VOLVULUS

A
  • an obstruction resulting from faulty midgut rotation
  • will result in/causes:

pain

bilious vomiting

GI bleeding

Failure to thrive

**This is a surgical emergency** so tht no further degeneration of the bowl will occur

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4
Q

HINDGUT ABNORMALITIES

A

Congenital Megacolon

Imperforate Anus

Patent Urachus (sinus, diverticulum, cyst)

Volvulus

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5
Q

developmental abnormlities of the stomach

PYLORIC STeNOSIS

A
  • most common
  • more common in males

1 in 150 males; 1 in 750 females

  • results from a muscular thickening of the pylorus
  • muscles become hypertrophied which causes the obstruction

SIGNS: Projectile Vomiting

onstruction of the passage of food

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6
Q

when does the exophagus reach its final length?

A

7th week

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7
Q

Development of the Esophagus

A

1-develops from the foregut

2-located behind the pharynx

3-division of the trachea from the esophagus occurs by the esophageal septum

4- Initially the esophagus is short, but it reaches it’s final length by the 7th week

5-musculature comes from connective tissue from the pharyngeal arches

6-1st solid tube that opens by the end of the embryonic period

7-covered with smooth muscle

8-invervated by branches of the vagus nerve which is supplied by the pharyngeal arches

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7
Q

Anomalies of the Midgut

A

Omphalocele

Gasorschesis

umbilical hernia

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8
Q

when does esophageal atresia occur?

A

8th week

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8
Q

How does the lesser curvature grow?

A

RIGHT & CRANIALLY

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9
Q

Can see along with Down’s Syndrome/intestinal malrotation and/or cardiac defects:

A

ANnular Pancreas

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10
Q

Causes of hepatic abnormalities

EXTRAHEPATIC BILIARY ATRESIA

A
  • failure of the system itself to develop
  • infection in pregnancy
  • immunolog reaction late in fetal development
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10
Q

Development of the Spleen

A
  • develops from the mesentary that’s attatched to the stomach
  • the spleen is a vascular lymphatic organ
  • rotation of stomach moves the spleen to the left side of the abdominal cavity
  • spllen begins to develop as lobes in the fetus
  • primitive connective tissue involved with these lobes; lobes disappear before birth
  • it’s the connective tissue that provides tissue framework for the spleen to actually develop
  • begins to develop during the 5th week but does not gain recognition until early in the fetal period
  • spleen functions as a hematopoetic organ until later in fetal life
  • Interesting that the spleen does retain its potential for developing RBC’s even into adult life
  • good back-up organ in terms of RBC production
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10
Q

development of large and small intestine

A

at the 10th week, the intestines/intestinal loop retracts back into the abdominal cavity where it rotates an additional 180 degrees counterclockwise

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11
Q

can cause obstruction of duodenum

A

Annular Pancreas

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12
Q

GASTROSCHESIS

A
  • results from the incomplete closure of the lateral folds of the abdomen during the 4th week
  • abdominal contents protrude to the right of the umbilical cord -
  • area is weakened by regression of the right umbilical vein
  • intestines are not covered by a membrane

1/10,000 births

occurs more in males

typically not associated ith any other genetic/chromosomal anomalies

result of a weakened area where the right umbilical vein regresses

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13
Q

the pancreas starts out as 2 buds and with the rotation of the stomach, they (buds) come together and actually form the pancreas

A

pancreas

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15
Q

Omphalocele

(ventral wall defect)

A

presistence of herniated contents into the proximal part of the umbilical cord

  • 1/5000 births
  • abdominal cavity is small in these babies
  • omphalocele is covered by a membrane or sac in the epithelium f the ubiical cord which comes from the amnion
  • occurs because the the contents don’t go back into the abdominal cavity
  • a=but also caused by impaired growth of muscle and skin of abdomoinal wall that contributes to it as well
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15
Omphalocele
1/5000 small omphalocele that doesn't include the liver 1/10000 babies will include the liver (typically a much larger defect
16
17
The gut tube is fully formed at the end of what week?
6th
18
Inferior part of the endoderm gives rise to
1-foregut 2-midgut 3-hindgut
20
Abnormalities of the Hindgut Congenital Megacolon
Congenital Megacolon Hirschsprung's Disease Aganglionic Mega Colon
21
Development of the DUODENUM
- Duodenum is developed from the caudal part of the foregut and cranial part of the midgut - located distal to the common bile duct - becomes reduced during the 5th and 6th week as the cells proliferate - see it reopening during the 8th week of gestational age - if it does not reopen, it can result in duodenal stenosis or duodenal atresia
21
Development of Liver and Gallbladder development from the foregut
- Liver & Gallbladder develop from foregut early in the 4th week - 2- liver bud enlarges and divides into 2 parts a- cranial part-liver b-caudal part-gallbladder 3- bile ducts (4th week) -small part of the liver bud will become the commn bile duct
22
Mortality rate in omphalocele is 25% associated with other anomalies
Other anomolies associated with omphalocele include 1-neural tube defects 2-cardiac defects 3-trisomy 18 4-urogenital problems When you have an omphalocele---look for other abnormalities
24
Extrahepatic Bilary Atresia Hepatic abnormalities
- Not common but serious - 1 in 5,000 to 20,000 live births - The most common form is total obliteration f the bile ducts -
26
development of large and small intestine
8-retracting midgut completes the rotation as cecum is positioned just inferior to the liver 9-cecum is displaced inferiorly pulling down the prominal hindgut to form ascending colon 10- descending colon is fixd ont he left side of posterior abdominal wall 11-jejunum, ileum, transverse and sigmoid colons remain suspended by the mesentary; so they aren't attatched to the abdominal wall 12-appendix is formed as a sprout on the cecum
27
extrahepatic biliary atresia signs
jaundice soon after birth \*\*Clay colored stools\*\* (specific characteristics to biliary atresia) -Urine is dark colored
29
Abnomalities of the Hindgut Imperforate Anus
Imperforate Anus 1/5,000 abnormal development of anorectal septum causes: Failure of the anal membrane to rupture in the 8th week - an anal pit persists, but does not communicate with the anal canal - associated with incomplete seperation of cloaca into the urogenital and anorectal parts
30
Hepatic Biliary atresia
will require surgery prognosis is somewhat palliative 70% still have problems as they continue to develop
31
what deformity occurs right of the umbilical cord?
Gastroschesis
32
Howdoes the greater curvature move?
LEFT and CAUDALLY
34
Folding of the Embryo
1-Occurs at the 3rd week. 2-Endoderm gives rise to the lining f the GI tract 3-Inferior part of the endoderm will give rise to a-foregut b-midgut c-hindgut 4-the gut tube is fully formed at the end pf the 6th week 5-buccopharyngeal membrane becomes the mouth 6-cloacal membrane becomes the: a-anus b-urogenital system 7-septum transversum seperates the thoracic and abdminal cavities
35
what structure seperates the thoracic and abdominal cavities?
Septum Transversum
37
Liver and gallbladder
Hepatic Abnormalities Extrahepatic Biliary Atresia
38
Development of Rectum & Urogenital Sinus
1-Cloaca becomes the anus Cloaca is divided into 2 parts by the urorectal septum a-anorectal canal b-urogenital sinus 2-urogenital sinus will give rise to the bladder and pelvic urethra 3-the perineum is created by the fusion of the urorectal septum with the cloacal membrane
40
Endoderm gives rise to the
Lining of the GI tract
41
Midgut Abnormalities
Omphalocele Umbilical Hernia Gastroschesis
42
Development of the liver
The quantity of oxygenated blood rom the umbiical vein into the liver determines the developmental and functional segmentation of the liver
43
when does the the duodenum open to form the duodenum?
8th week
45
Development of Hindgut Deviations of the hindgut
- Includes the left 1/3 ti 1/2 of transverse colon, descending and sigmoid colon, recum and anal canal - Epithelum of urinary bladder - most of the the urethra
46
hingut includes what parts of the colon?
left 1/2 to 1/3 of transverse Colon descending colon sigmoid colon epithelium of the urinary bladder most of the urthera
47
Abnormalities of the Esophagus
Esophageal Atresia Association with TE FISTULA Deviation of tracheoesophageal septum in the posterior direction Imcomplete seperation of esophagus from endotracheal tube - isolated esophageal atresia without a fistula that may be associated with other congenital anomolies - other congenital anomolies may include a-rectal atresia b-abnormalities of urogenital system - in these cases, atreia will reult from the failure of the esp[hagus to re-open during the 8th week of development - a fetus with aeophageal atresia is unable to swallow amniotic fluid which results in polyhydramnious int he mother
48
When does Gastroschesis occur?
During the 4th week
49
Esophageal Stenosis
resuts from a narrowing of the lumen of the esophagus itself -usually seen in the distal 1/3 o the esophagus
50
Causes of Esophageal Stenosis
results from the incomplete re-opening (recanalization) of the esophagus during the 8th week -a lack of blood vessels developing in the affected area contributes to the stenosis (when you have a lack of blood vessels that develop n this area, it can result in atrophy in a segment of the esophageal wall, limiting its opening)
51
Where does the esphagus develop from?
FOREGUT
53
Development of the stomach
1-develops from the abdominal foregut in the 4th week 2-during the 6th week a-the dorsal wall of the stomach grows faster than the ventral wall; the faster growing dorsal wall becomes the greater curvature of the stomach b-the ventral wall is called the lesser curvature c-the greature curvature includes the fundus and the indentation of the stomach or cardiac incisor 3-the stomach rotates 90 degrees clockwise (helps to get stomach in the right position) a-greature curvature will moce LEFT and CAUDALLY b-lesser curvature will move RIGHT and CRANIALLY 4-Rotation causes the duodenum to become "C" shaped and displaces it to the right when it becomes attatched to the dorsal body wall 5-development of the greater omentum
55
Development of the Pancreas
1-develops from the foregut 2-develops as 2 buds a-dorsal pancreatic bud b-ventral pancreatic bud 3-pancreas forms:as stomach & adjacent duodenum rotate when the buds attach and fuse to form the pancreas 4-ducts within the buds also fuse creating the main pancreatic duct
56
what occurs from an imcomplete closure of the lateral folds during the 4th week?
gastroschesis
58
Hepatic Abnormalities
extrahepatic biliary atersia
59
the ventral and dorsal wallos of the stomach are growing/forming when?
6th week
60
Development of the Small and Large Intestine
5th week-the ileum is distinguishable -Ileum elongates rapidly which causes/results in: a-causes midgut to fold dorsoventrally (back to belly) = primary intestinal loop b-cranial part of loopmost of the ileum c-caudal part will become the ascending and transverse colon - the top of primary intestinal loop is attatched to the umbilicus by the vitalline duct - contunued elongation of the midgut and dramatic growth of the liver which forces the primary intestinal loop to herniate into the umblicus
61
How are abnormalities of the esophagus usually found?
typically have trouble passing a tube-you will meet resistence/obstruction
62
Development of the small and large intestine
THe small intestine is now elongating to form the jejunum, jejuanal-ileal loop and cecum and appendix
63
What causes imperforate anus?
abnormal development failure of membrane to rupture during the 8th week
64
\*\*The Intestine develop in the umbilicus as the primary intestinal loop herniates and also rotates 90 degrees counterclockwise
65
what does the cloacal membrane become?
1-anus 2-urogenital system
66
What week does the rectum form? (urorectal septum fusing withthe cloacal membrane)
7th
67
Caused by weakened by regression of right umbilical vein
Gastroschesis
68
health assessment in=mperforate anus
check patency-1 rectal temp membrane can be broken and it will be ok if there is a connection between the rectum and anus
69
when does the stoach develop?
4th week
70
Development of the Midgut
Small Intestine Cecum appendix ascending colon right 1/2 to 2/3 of transverse colon Most of duodenum
71
Liver
- by the 9th week, the liver counts for about 10% of the total body weight of the fetus - bile starts to enter the duodenum after the 12th week - bile gives meconium dark green color - meconium begins to form at 6 weeks of age
72
Increase int he size between 5&10 weeks is due to:
the hematopoetic activity in the liver
73
Pancrease abnormalities
Annular Pancreas
74
Umbilical Hernia
- does not close off to the intestinal cavity - consists of greater omentum and some small intesine - Protrudes during crying - not repaired unless persists beyond age 3-5 - see umbilicus close off to the intestinal cavity by the 10th week of gestation - can be various sizes and range 1-5cm - if can be reduced or not will determine how soon surgery will be done (or if surgery will be done)
75
Annualar Pancreas Disorders of the Pancreas
- Thin flat band of pancreatic tissue that surrounds the decending (second) part of the duodenum - it is another ventral pancreatic bud that grows; this bud will fuse with dorsal bud forming a ring around the duodenum - can cause obstruction of the duodenum - infants that have an annular will present with complete or partial bowel obstruction - Can see Down's Syndrome with intestinal mal-rotation or cardiac defects - females are more affected than males
76
Symptoms of a patent Urachus Abnormalities of the HINDgut
leakage of urine around the umbilicus UTI Peritonitis (with perforation of the urachus) Repaired surgically (sometimes urgently)
77
When does folding of the embryo occur?
3rd week
78
abnormalities in stomach:
Pyloric Stenosis