GIT I Flashcards
CONGENITAL ABNORMALITIES
______, _____, and duplications may occur in any part of the GI tract. when present within the esophagus they are discovered shortly after birth, usually due to regurgitation during feeding
atresia, fistula, and duplications
CONGENITAL ABNORMALITIES
_______, a segment of the esophagus does not develop, leaving only a thin, noncanalized cord and causing mechanical obstruction
atresia
CONGENITAL ABNORMALITIES
________ is an incomplete form of atresia in which the lumen is markedly reduced in caliber as a result of fibrous thickening of the wall
stenosis
CONGENITAL ABNORMALITIES
_______ tissues (developmental rests) are common in the GI tract. The most frequent site of ectopic gastric mucosa is the upper 3rd of the esophagus where it is referred to as an inlet patch.
ectopic tissue
CONGENITAL ABNORMALITIES
__________ is a blind outpouching of the alimentary tract that communicates with the lumen and includes all 3 layers of the bowel wall
true diverticulum
CONGENITAL ABNORMALITIES
_____________ generally presents between the 3rd and 6th weeks of life as new-onset regurgitation, projectile nonbilious vomiting after feeding, and frequent demands of refeeding
congenital hypertrophic pyloric stenosis
CONGENITAL ABNORMALITIES
________ diseases causes functional obstruction of the colon due to failure of ganglion cells to migrate to the wall of the colon resulting from mutation in the receptor tyrosine kinase
Hirschsprung disease
CONGENITAL ABNORMALITIES
Hirschsprung disease
Heterozygous loss-of-function mutations in the receptor tyrosine kinase ______ account for the majority of familial and approximately 15% of sporadic Hirschsprung diseases.
receptor tyrosine kinase RET
CONGENITAL ABNORMALITIES
HIRSCHSPRUNG
diagnosis of Hirschsprung disease requires histologic confirmation that _________ are absent within the affected segment
disease limited to the rectosigmoid is termed _________
proximal extension are termed as ______________
ganglion cells
short-segment Hirschsprung disease
long-segment Hirschsprung disease
ESOPHAGUS
Esophageal obstruction
________- describes functional obstruction of the esophagus by intense, high amplitude, uncoordinated contractions of inner circular, and outer longitudinal smooth muscle
nutcracker esophagus
ESOPHAGUS
Esophageal obstruction
_________- also known as corkscrew esophagus is due to the appearance on barium swallow, is characterized by repetitive simultaneous contractions of the distal esophageal smooth muscle
diffuse esophageal spasm
ESOPHAGUS
Esophageal obstruction
__________ including high resting pressure or incomplete relaxation may be presented as an isolated anomaly or accompany nutcracker esophagus or diffuse esophageal spasm
lower esophageal dysfunction
ESOPHAGUS
Esophageal obstruction
in the upper-esophagus, webs may be accompanied by iron-deficiency anemia, glossitis, and cheilosis, as part of ___________
plummer-vinson syndrome
ESOPHAGUS
_______ is characterized by the triad of incomplete lower esophageal sphincter relaxation, increased lower esophageal sphincter tone, and aperistalsis of the esophagus
achalasia
ESOPHAGUS
_______ achalasia may arise in Chagas disease, in which trypanosoma cruzi infection causes destruction of the myenteric plexus, failure of peristalsis, and esophageal dilation
secondary achalasia
ESOPHAGUS
logitudinal mucosal tears near the gastroesophageal junction called _________ are most often associated with severe retching or vomiting secondary to alcohol intoxication
mallory-weiss tears
ESOPHAGUS
chemical and infectious esophagitis
Symptoms range from self-limited pain, particularly on swallowing called __________, hemorrhage, structure, or perforation in severe cases
less severe chemical injury to the esophageal mucosa can occur when medicinal pills lodge and dissolve in the esophagus, a condition termed ____________
odynophagia
pill-induced esophagitis
ESOPHAGUS
chemical and infectious esophagitis (Morphology)
candidiasis is characterized by adherent, gray white _______ composed of densely matted fungal hyphae, and inflammatory cells covering the esophageal mucosa
pseudomembranes
ESOPHAGUS
chemical and infectious esophagitis (Morphology)
histologic features of esophageal ____________ are similar to those of skin and include basal epithelial cell apoptosis, mucosal atrophy, and submucosal fibrosis without significant acute inflammatory infiltrates
graft vs host disease
ESOPHAGUS
reflux of gastric contents into the lower esophagus is the frequent cause of esophagitis and the most common outpatient GI diagnosis in the US
reflux esophagitis
ESOPHAGUS
reflux esophagitis
transient lower esophageal sphincter relaxation is thought to be a major cause of _________
GERD
ESOPHAGUS
________ is a form of acute eosinophilic dominated esophageal inflammation associated with atopic disease
in addition to GERD like symptoms, patients experience food impaction, dysphagia, and vomiting
eosinophilic esophagitis
ESOPHAGUS
______________ are caused by portal hypertension which is due to impaired blood flow, through the portal venous system and liver
Morphology:
torturous dilated veins within the mucosa and submucosa of the distal esophagus and proximal stomach
Clinical manifestations
Variceal hemorrhage
esophageal varices
ESOPHAGUS
_________ esophagus is a complication of chronic GERD that is characterized by intestinal metaplasia within the esophageal squamous mucosa and is associated with an increased risk of cancer
Barret Esophagus