Congential Anomalies and Esophagus Path Flashcards

1
Q

What organs should be evaluated promptly if a GI congenital anomaly is noticed? (5)

A
Liver
Gall Bladder
Pancreas
Lungs
Spleen
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2
Q

Two most common types of GI atresia

A

Esophageal atresia (Tracheoesophageal fistula)

Imperforate anus (intestinal atresia)

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3
Q

GI Tract Ectopia

Definition and Examples (3)

A

Nodules of tissue from one organ misplaced on another organ (developmental rests)

Inlet Patch: upper third of esophagus
Ectopic Pancreatic Tissue
Gastric Heterotopia

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4
Q

Omphalocele vs Gastroschisis

A

Omphalocele is herniation of viscera into ventral membranous sac from failure of abdominal musculature to close

Gastroschisis is when the viscera is herniated all the way through from the peritoneum to exposed skin

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5
Q

Meckel Diverticulum

Pathogenesis (2), Clinical Features (4)

A

Failed involution of the Vitelline duct forming true diverticulum

2 feet from ileocecal valve
2 inches long
2x as common in males
Symptomatic by age 2 (but mostly asymptomatic)

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6
Q

Pyloric Stenosis

Correlations (3), Presentation (4)

A

Most common in males
Turner Syndrome
Trisomy 18

Presents in babies (3-6 weeks)
Regurgitation and projectile vomiting
Frequent feeding demands
Firm ovoid abdominal mass

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7
Q

Hirschsprung Disease
Pathogenesis, Morphology, Association, and Clinical Features (6)
*means life threatening

A

Failure of neural crest cells to migrate from cecum to rectum

Ganglion cell absence
Megacolon

Trisomy 21 (Downs Syndrome)

Constipation
Abdominal distension
Bilous vomit
Enterocolitis*
Perforation*
Peritonitis*
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8
Q

Esophageal Obstruction Causes

Functional (3) and Mechanical (3)

A

Functional: peristalsis abnormality
Nutcracker Esophagus
Diffuse Esophageal Spasm
Systemic Sclerosis

Mechanical: physical blockage
Stricture
Stenosis
Mass

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9
Q

Achalasia

Characteristics (4), Primary and Secondary (2) Descriptions

A

Incomplete Lower esophageal sphincter relaxation
Increased LES tone
Aperistalsis of esophagus
Bird beak sign on Barium swallow CXR

Primary
Degeneration of ganglion cells in distal esophagus

Secondary
Chagas infection that destroys distal myenteric plexus
Causes dilation of esophagus

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10
Q

Infectious Esophagitis Causes

Healthy (1) and Immunocompromised (5)

A

Herpes Simplex Virus (in healthy people)

Immunocompromised People:
Cytomegalovirus
Herpes Simplex Virus
Candida albicans
Mucor
Aspergillus
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11
Q

Chemical Esophagitis

Presentation (4) and Causes (4)

A

Odynophagia
Stricture
Hematemesis
Perforation

Pill Induced
Graft vs Host Disease
Chemotherapy
Radiation therapy

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12
Q

Reflux Esophagitis

Prevalence, Cause and Underlying Etiologies (4)

A

Most common esophagitis

GERD

Increased abdominal pressure
Obesity
Sliding hiatal hernia
Gastroparesis

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13
Q

Eosinophilic Esophagitis

Symptoms (3), Associations (2) and Diagnosis

A

Food impaction
Dysphagia
Feeding intolerance (infants)

Atopic dermatitis
Seasonal/Food allergies

EGD showing corrugated ring esophagus

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14
Q

Esophageal Varices

Relevant Anatomy, Pathogenesis (4) and Clinical Features (2)

A

Portal vein has collateral circulation with caval system that connects it to Esophageal Veins

Liver cirrhosis causes Portal HTN which backs up blood into Esophageal veins forming submucosal/subepithelial varices

Variceal hemorrhage is leading COD in cirrhosis
High rate of hemorrhage recurrence

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15
Q

Barrett Esophagus

Etiology, Pathogenesis (2), and Clinical Features (3)

A

Columnar metaplasia caused by chronic GERD

Refluxed acid causes squamous to columnar metaplasia
As GERD continues, dysplasia may occur leading to adenocarcinoma

Diagnosed by endoscopy with biopsy
Progression to adenocarcinoma is greatest concern
Seen most in white males

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16
Q
Esophageal Adenocarcinoma
Risk Factors (3), Pathogenesis (3), Clinical Features (3)
A

Barrett’s Esophagus (GERD)
Tobacco
Radiation

Stepwise progression via genetic/epigenetic changes
TP53 mutation
Downregulation of CDKN2A

Dysphagia
Odynophagia
Hematemesis

17
Q
Squamous Cell Carcinoma
Risk Factors (6) Clinical Features (5)
A
Alcohol**
Tobacco**
Tylosis
Achalasia
Plummer-Vinson syndrome
Caustic injury
Progressive Dysphagia
Odynophagia
Esophageal Obstruction
Hoarseness
Cough
18
Q
Plummer Vinson Syndrome
Clinical Features (6)
A
Esophageal Web
Esophageal Squamous Cell Carcinoma
Iron deficiency Anemia
Glossitis
Cheilitis
Spoon nails