17 Gastrointestinal Tract Flashcards

1
Q

What are the majro categories of esophagitis?

A

Infectious
Chemical
Radiation
Iatrogenic

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2
Q

What is Boerhaave syndrome?

A

Distal esophageal rupture with mediastinitis

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3
Q

What are causes of secondary achalasia?

A
Chaga's disease (Trypanasoma cruzi)
Diabetic autonomic neuropathy
malignancy
amyloidosis
sarcoidosis
polio
surgical ablation of dorsal motor nuclei
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4
Q

What is the mechanism by which the lower esophageal sphincter relaxes?

A

NO nad VIP relase from inhibitory neuros and inhibition of normal cholinergical signally allows LES to relax

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5
Q

What are the types of congenital anomlies that can present in the GI tract?

A
Atresia
Fistulae
Duplications
Hernia
Omphalocele
Gastorchisis
Ectopia
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6
Q

What abnormalities are associated with esophageal atresia?

A

congenital heart defects
GU malformation
neurological disease

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7
Q

What are other more common causes of stenosis?

A
GERDD
irradiation
scleroderma
caustic injury
congenital stenosis
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8
Q

How does omphalocele occur?

A

Incomplete closure of abdominal musculature and abdominal viscera herniate into ventral membranous sac

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9
Q

Which of omphalocele and gastroschisisis is more associated with other congenital defects?

A

Omphalocele

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10
Q

How does gastroschisis occur?

A

All layers of hte abdominal wall fail to form.

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11
Q

Where does the inlet patch occur?

A

Upper third of esophagus

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12
Q

Where is the most common sites of pancreatic ectopia?

A

Stomach or esophagus

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13
Q

Where else does gastric heterotopia occur

A

small bowel or colon or esophagus

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14
Q

What causes Meckel diverticulum

A

Failure of involution of the vitelline duct

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15
Q

What are some of the molecular pathways assoicated with Hirschsprung’s?

A

RET heterozygous loss of function mutations; mutationsi n RET ligand, glial-derived neurotrophic factor, endothelin, endothelin receptor

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16
Q

What are the different types of esphageal rings?

A

Type A - above GE junction, squamous mucosa

Type B - at squamocolumnar junction, gastric cardia-typ mucosa

17
Q

What are the major features of Paterson=Brown-Kelly or Plummer-Vinson syndrome?

A

upper esophageal webs, iron deficiency anemia, glossitis and cheilosis

18
Q

What is the morphology of mucosal webs and how do htey different from Schatski rings?

A

Esophgeal webs - ledge-like, semicircumferential, eccentric lesions. Schatski rings are circumferential and thicker and include mucsoa, submucosa and can include muscularis propria