Path II Flashcards

1
Q

What is the most common atresia and fistula in the GI tract

A

blind upper esophagus and fistula between lower esophagus and trachea

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2
Q

first signs of esophageal atresia and tacheoesophageal fistula

A

polyhydramnios

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3
Q

Sx pyloric stenosis

A

projectile non-bilious vomiting, 2-8 wks of age

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4
Q

how common is a pyloric stenosis

A

US 1 in 600

M4:1F

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5
Q

Tx for pyloric stenosis

A

NOT gastrectomy

simple muscle sectioning

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6
Q

duodenal atresia is associated with what?

first sign?

A

30% have trisomy 21

polyhydramnios

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7
Q

where do most duodenal atresias occur

A

ampulla of vater

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8
Q

double bubble sign

A

annular pancreas

duodenal atresia

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9
Q

most common form of congenital intestinal atresia? what causes it?

A

imperforate anus

failure of cloacal diaphragm to involute

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10
Q

what is omphalocele

A

failure midgut to return to abdominal cavity, incomplete umbilicus, covered by amnion

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11
Q

risk factors for having a child with omphalocele

A

advanced maternal age

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12
Q

what is a diaphragmatic hernia and associated with?

A

incomplete formation of diaphragm

associated with pulmonary hypoplasia

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13
Q

what is gastroschisis

A

defect in abdominal wall so that gut is lateral to umbilicus and not covered by amnion

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14
Q

what are ectopic tissue rests

A

gastric or pancreatic tissue that can lead to inflammation, bleeding, scarring and obstruction

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15
Q

what is an “inlet patch”

A

heterotopic gastric mucosa in upper 1/3 esophagus

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16
Q

What is the most common malformation of the small bowel

A

meckel diverticulum from failure involution of the vitelline duct

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17
Q

where are meckel diverticulums

A

otehr side of mesentery “antimesenteric”

in distal ileum within 1 m of ileocecal valve

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18
Q

what is a true meckel diverticulum

A

contains all three layers of the bowel wall (mucosa, submucosa and muscularis)

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19
Q

Tx for vitelline duct abnormalities

A

normally close by 10 weeks

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20
Q

Sx meckel diverticulum (96% asymptomatic)

A

obstruciton )intussusception), bleeding from peptic ulceration of adjacent mucosa, pain/inflammation

21
Q

rule of 2s is what and applies to what?

A
meckel diverticulum
2% popn
within 2 ft ICV
approx 2in long
2M:1F
usually Sx by 2 y.o
22
Q

Dx meckel diverticulum in children

A

99mTc Nuclear Medicine Scan

concentrates in gastric mucosa and urine

23
Q

What causes Hirschsprung Disease

A

part of the colon lacks Meissner and Auerbach plexuses and ganglion cells
no migration of neural crest cells from cecum to rectum during embryogenesis- ganglion cells undergo premature death

24
Q

What genes have been identified in hirschsprung disease

A

8, especially Rtk RET

25
what part is always affected in megacolon
rectum
26
population affected by megacolon
1/5,000 live birth 4M:1F | up to 10% in trisomy 21
27
imagin for hrischprungs
barium enema
28
what is the in the mucosa layer of esophagus
epithelium- squamous non-keratinizing Lamina Propria- Intm zone of loose CT and capillaries that connects epithelium with supporting framework of the muscularis mucosae
29
what is found in the submucosa of esophagus
smooth muscle, blood vessels, lymph, nerves and submucosal glands
30
describe the muscularis propria of esophagus
external starts as skeletal muscle and gradually transitions into smooth muscle internal layer has circular transverse smooth muscle
31
what is oropharyngeal dysphagia
difficulty transferring food to the esophagus or in intitiating swallowing
32
what is esophageal dysphagia
difficulty transporting down esophagus (food gets stuck) "nutcracker esophagus"
33
what are the types of pain assoc with esophagus
pyrosis (heartburn) odynophagia (pain while swalloing) atypical chest pain ("atypical" for coronary artery disease)
34
what is pummer vinson syndrome
upper esophageal webs, Fe deficiency anemia, glossitis, cheilosis
35
esophageal webs are most common where
upper esophagus
36
what is a schatzki ring in esophagus
circumferential A is above GEJ B is below GEJ
37
schatzki rings common in what sex
W >40
38
95% of hiatal hernias are what type
sliding (above fundus where esophagus connects)
39
what lesions are related to motility dysfunction in esophagus
hiatal hernia, diverticula, mallory-weiss tear and achalasia
40
what is triad of esophageal achalasia
incomplete LES relaxation, increased LES tone, aperistalsis of the esophagus
41
causes of achalasia
primary is idiopathic | secondary to chagas disease, DM, polio
42
signs of achalasia
dysphagia regurig and pain behind sternum weight loss
43
achalasia increases risk for?
SCC
44
Dx achlasia
barium swallow and manometry
45
CREST syndrome
``` calcinosis raynauds esophageal dysfunction (fibrous replacement of lower 2/3 esophagus and loss of LES) sclerodactyly telangiectasias ```
46
anti-Scl 70 topoisomerases
CREST syndrome
47
presentation of mallory weiss laceration
alcoholic severe retchin or violent vomiting UGI bleeds that heal promptly- mucosal longitudinal tears)
48
Signs boerhaave syndrome
``` vomiting thoracic crepitus increased esophageal intraluminal pressure hematemesis and chest pain perforation of esophagus on L side ```
49
imaging booerhave syndrome
CXR- pneumomediastinum, L pleural effusin, L pneumothorax | esophagram- extravastaion of contrast material