GIT: Esophagus Flashcards

(31 cards)

1
Q

describe esophgeal atresia

A
  • non-canalization of portion of esophagus (atresia/stenosis)
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2
Q

esophageal atresia is commonly associated with ____

A

esophageal atresia is commonly associated with tracheo-esophageal fistula (TEF)

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3
Q

list the clinical symptoms of esophageal atresia

A
  • clinical symptoms:
    • excessive drooling of saliva
    • aspiration pneumonia
    • choking and cyanosis
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4
Q

describe esophageal webs and rings

A

protrusions of mucosa into the lumen

  • upper esophagus = webs
    • covered by squamous mucosa with vascularized core
  • lower esophagus = Schatzi ring
    • undersurface have columnar epi.
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5
Q

describe the triad seen in Plummer-Vinson syndrome (aka Kelly Patterson syndrome)

A
  • triad:
    • iron deficiency anemia
    • esophageal webs
    • atrophic glossitis
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6
Q

Plummer-Vinson syndrome has a high risk for ____

A

Plummer-Vinson syndrome has a high risk for squamous cell carcinoma of esophagus

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7
Q

patients with Plummer-Vinson sydrome present with ____ and ____

A

patients with Plummer-Vinson syndrome present with koilonychia (spoon nails) and splenomegaly (compensation for iron def.)

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8
Q

describe the treatment for Kelly Patterson syndrome

A
  • treatment:
    • iron
    • endoscopic dilatation
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9
Q

list the 3 main features of achalasia/cardiospasm

A
  • 3 main features:
    • partial or incomplete relaxation of LES with swallowing
    • aperistalsis
    • increased resting tone of LES
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10
Q

one of the 2 primary causes of achalasia is the loss of _____ of the LES

A

one of the primary causes of achalasia is the loss of intrinsic inhibitory innervation of the LES

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11
Q

one of the primary causes of achalasia is the loss/absence of _____

A

one of the primary causes of achalasia is the loss/absence of ganglion cells in myenteric plexus

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12
Q

list the causes of secondary achalasia (pseduoachalasia)

A
  • Chagas disease (Trypanosoma cruzi)
  • diabetic autonomic neuropathy
  • infiltrative disorders: malignancy, amyloidosis, sarcoidosis
  • spinal motor neurons: polio, surgical ablation
  • Down syndrome
  • autoimmune disease
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13
Q

describe Mallory Weiss syndrome

A
  • longitudinal mucosal tears at esophagogastric junction
  • frequently in alcoholics after bout of severe retching
  • inadequate relaxation of LES during vomiting
  • hematemesis
  • usually heals but sometimes fatal
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14
Q

in Mallory Weiss syndrome, there are ____ at the esophagogastric junction

A

in Mallory Weiss syndrome, there are longitudinal mucosal tears at the esophagogastric junction

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15
Q

Mallory Weiss syndrome is commonly seen in ___ after bouts of ____

A

Mallory Weiss syndrome is commonly seen in alcoholics after bouts of severe retching

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16
Q

in Mallory Weiss syndrome, there is inadequate ____ of the ____ during vomiting

A

in Mallory Weiss syndrome, there is inadequate relaxation of the LES during vomiting

17
Q

list irritants that can cause esophagitis

A
  • irritants:
    • alcohol
    • acids
    • alkalis
18
Q

list complications of reflux esophagitis

A
  • complications:
    • bleeding
    • stricture
    • aspiration pneumonitis
    • Barrett esophagus & adenocarcinoma
19
Q

describe the image

A

reflux esophagitis with scattered intraepithelial eosinophils and mild basal zone expansion

20
Q

list 1 fungal and 2 viral causes of esophagitis

A
  • fungal:
    • Candida
  • viral:
    • Herpes simplex
    • CMV
21
Q

Barrett esophagus is replacement of esophageal ____ mucosa with metaplastic _____ with ____

A

Barrett esophagus is replacement of esophageal squamous mucosa with metaplastic columnar epithelium with goblet cells

22
Q

Barrett’s esophagus leads to an increased risk for ____; the risk is related to ____

A

Barrett’s esophagus leads to an increased risk for adenocarcinoma; the risk is related to the length of Barrett’s mucusa

23
Q

in Barrett’s esophagus screening with biopsy:

if there is no dysplasia, ____

if there is low grade dysplasia, ____

if there is high grade dysplasia, ____

if there is adenocarcinoma, _____

A

if there is no dysplasia, continue screening

if there is low-grade dysplasia, more frequent screening

if there is high-grade dysplasia, definitive therapy, resection or ablation

if there is adenocarcinoma, resection

24
Q

esophageal varices are caused by dilated tortuous veins in the ___ and ___ of the lower esophagus (and prox. stomach) and is associated with ____

A

esophageal varices are caused by dilated tortuous veins in the mucosa and submucosa of the lower esophagus (and prox. stomach) and is associated with portal HTN

25
describe what is seen in the image
**esophageal** **varices**
26
describe what is seen in the image
esophageal varices
27
name diets that lead to higher risk of SCC
* diet * vit. deficiency * A, C, riboflavin, thiamine, pyridoxine * fungal contamination * high nitrite content
28
list lifestyles that lead to a higher risk of SCC
* lifestyle: * alcohol * tobacco use * HPV
29
list esophageal disorders that lead to a higher risk of SCC
* esophageal disorders: * long-standing esophagitis * achalasia * Plummer-Vinson syndrome
30
list genetic changes that lead to higher risk for SCC
* genetics: * Celiac disease * ectodermal dysplasia (Tylosis)
31
\_\_\_\_ is the precursor lesion for adenocarcinoma of the esophagus
**Barrett's esophagus** is the precursor lesion for adenocarcinoma of the esophagus