Pathology of the GI Tract- SI and Colon (1) Flashcards

1
Q

what are the layers of the GI tract?

A

mucosa, submucosa, muscularis, and serosa

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2
Q

what are the components of the mucosa of the GI tract?

A

epithelium, lamina propria, and a thin smooth muscle layer called the muscularis mucosa

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3
Q

the presence of congenital GI disorders should prompt what?

A

evaluation of other organs because many organs develop simultaneously during this same time frame

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4
Q

what is a common congenital anomaly that is commonly associated with other congenital malformations, particularly cardiac defects?

A

Tracheoesophageal (TE) fistula

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5
Q

what is another congenital malformation that is related to a TE fistula?

A

esophageal atresia

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6
Q

what is the most common form of a TE fistula?

A

EA with a distal TE fistula

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7
Q

why do TE fistulas occur?

A

due to abnormal septation of the caudal foregut during the 4th and 5th weeks of embryonic development

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8
Q

what is Meckel diverticulum?

A

failed involution of the vitelline duct

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9
Q

what is the vitelline duct?

A

it connects the lumen of the developing gut to the yolk sac

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10
Q

how can you remember the characteristics of Meckel diverticulum?

A

the rule of 2’s

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11
Q

what are some complications associated with Meckel diverticulum?

A

the mucosal lining of meckel diverticula could be ectopic pancreatic or gastric tissue; the ectopic gastric tissue could secrete acid causing peptic ulceration of adjacent small intestinal mucosa

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12
Q

who is more likely to have pyloric stenosis?

A

male»females; monozygotic twins»dizygotic twins; increased risk in 45, XO and Trisomy 18

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13
Q

what is pyloric stenosis associated with?

A

use of antibiotics: arythromycin and azithromycin in the mom during pregnancy

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14
Q

how does pyloric stenosis present?

A

generally between the 3rd and 6th weeks of life as new onset regurgitation, projectile nonbilious vomiting after feeding, and frequent demands for refeeding

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15
Q

what is occurring anatomically in cases of pyloric stenosis?

A

the gastric outflow tract is obstructed by hyperplasia of the pyloric muscularis propria

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16
Q

what is Hirschspring disease?

A

aka aganglionic megacolon; there is abnormal migration or premature death of enteric ganglion cells

17
Q

what may Hirschspring disease occur in combination with?

A

other developmental abnormalities such as down syndrome and serious neurologic abnormalities

18
Q

how does hirschspring disease present?

A

with functional obstruction and the rectum is always involved

19
Q

intrinsic innervation of much of the GI tract is provided by the enteric nervous system; these enteric neurons are grouped into two plexuses, what are they?

A

the myenteric plexus (plexus of Auerbach) and the submucosal plexus (plexus of Meissner)

20
Q

which plexus is responsible for motility, especially the rhythm and force of the contraction of the muscularis?

A

myenteric plexus (plexus of Auerbach)

21
Q

which plexus is responsible for regulating digestive secretions and reacting to the presence of food?

A

the submucosal plexus (plexus of Meissner)