• Shuffle
    Toggle On
    Toggle Off
  • Alphabetize
    Toggle On
    Toggle Off
  • Front First
    Toggle On
    Toggle Off
  • Both Sides
    Toggle On
    Toggle Off
  • Read
    Toggle On
    Toggle Off
Reading...
Front

Card Range To Study

through

image

Play button

image

Play button

image

Progress

1/93

Click to flip

Use LEFT and RIGHT arrow keys to navigate between flashcards;

Use UP and DOWN arrow keys to flip the card;

H to show hint;

A reads text to speech;

93 Cards in this Set

  • Front
  • Back
most common site of ectopic gastric mucosa
upper 1/3 of esophagus

acid secretions can produce localized inflammation and discomfort
bronchial or parenchymal pulmonary tissue arising from the upper gut

usually present as masses
bronchogenic cyst or pulmonary sequestration
Immediate regurgitation when feeding attempted, usually discovered soon after birth

Commonly occur with fistula formation

Segment of esophagus is represented by only a thin noncanalized cord with a proximal blind pouch connected to the pharynx and a lower pouch leading to the stomach

Near tracheal bifurcation

Sometimes associated with presence of single umbilical artery
Esophageal atresia
Uncommon ledgelike protrusions of teh mucosa into the esophageal lumen

smicircumfrential, eccentric, and most common in the upper esophagus

Can be congenital or associated with long standing relux esophagitis, chrnic graft versus host disease, or blistering skin diseases
Esophageal web
esophageal web accompanied by iron deficiency anemia, glossitis, and ceilosis

attendant risk for postcricoid esophageal carcinoma
Paterson-Brown-Kelly/Plummer-Vinson syndrome
concentric plates of tissue protruding into the lumen of the distal esophagus

Most frequent in women over age 40

dysphagia usually provoked by bolting solid food
esophageal ring
esophageal ringabove the squamocolumnar junction of the esophagus and stomach
A ring
esophageal ring located at the squamocolumnar junction of the lower esophagus
Schatzki ring/B ring
fibous thickening of the esophageal wall, particularly the submucosa

Atroph of the muscularis propria

Ulcerated lining

History of gastoesophageal reflux, radiation, scleroderma, or caustic injury

Patient presents with progressive dysphagia
esophageal stenosis
"failure to relax"

aperistalsis, patial or complete relaxation of the LES with swallowing and increased resting tone of teh LES

May be caused by disorders of the dorsal motor nuclei, diabetic autonoic neuropathy, or infiltrative disorders

Progressive dilation of the esophagus

Myenteric ganglia usually absent from body of esophagus

progressive dysphagia; nocturnal regurgitation may occur; risk of developign squamous cell carcinoma
achalasia
Trypanosoma cruzi causes destruction of myenteric plexus of esophagus, duodenum, colon, and ureter

resultant dilation in these vicera
Chagas disease
Separation of diaphragmatic crura and widening of the space between teh muscular crura adn the esophageal wall

ulceration, reflux esophagitis, compromise of LES with regurgitation of peptic juices

incidenc increases with age
hiatal hernia
protrusion of the stomach above the diaphragm, which creates a bell shaped dilation bounded by the diaphragmatic narrowing
Sliding hiatal hernia
Separate portion of the stomach, usually along the greater curvature, enters the thorax through the widened foramen

Strangulation and obstruction of the stomach/bowel may occur
paraesophageal hiatal hernia
outpouching of the alimentary tract that contains all visceral layers

dysphagia, food regurgitation, mass in the neck, aspiration with resultant pneumonia
diverticula
outpouching of mucosa and submucosa only
false diverticula
diverticula occuring immediately above the UES

disordered cricopharyngeal motor function w/o GERD adn diminished sized of UES
Zenker diverticula
Diverticula near the midpoint of the esophagus
traction diverticula
diverticula immediately above the LES
Epiphrenic diverticulum
longitudinal tears in the esophagus at the esophagogastric junction or gastric cardia

history of prolonged vomiting such as in alcoholics

underlying hiatal hernia is predisposing factor

linear irregular lacerations oriented in the axis of the esophageal lumen usually found astride esophagogastric junction or in proximal gastric mucosa
hematemesis may occur
mallory weiss syndrome
esophageal rupture associated with lacerations

may be catastrophic event
Boerhaave syndrome
sufficiently prolonged or severe hypertension; induced formation of collateral bypass channels wherever portal and caval systems communicate

collaterals that develop inth eregion of the lower esophagus when portal blood flow is diverted through the coronary veins of the stomach into the plexus of esophageal subepithelial and submucosal veins-> azygos veins-> systemic circulation

Associated with cirrhosis of the liver
esophageal varices
tortuous dilated veins lying primarily w/in the submucosa of the distal esophagus and proximal stomach; vnous channels directly beneath th esophageal epithelium may also become massively dilated

irregular protrusion of the overlying mucosa it the lumen (collapsed in surgical/postmortem)

Rupure produces massive hemorrhage into the lumen, suffusion of the esophageal wall with blood

Usually no symptoms til rupture-> massive hematemesis
esophageal varices
inflammation of the esophageal mucosa

Largely occuring in western countries but also northern Iran and portions of China
esophagitis
reflux of gastric contents into the lower esophagus causes development of esophageal mucosal injury

hyperemia may be alteration; presence of inflammatory cells, basal zone hyperplasia, elongation of lamina propria papillae with capillary congestion, infiltrates of intraepithelial eosinophils

Adults over 40, dysphagia, heartburn, sometimes regurgitaiton of sour mash, hematemesis, or melena

Consequences of sevre reflux are bleeding, ulceration, development of stricture, and tendency to develop Barrett esophaus
Relux esophagitis (GERD)
Long standing gastroesophageal reflux, single most important risk factor for esophageal adenocarcinoma

Distal squamous mucosa s replaced by metaplastic columnar epithelium

Admixed with intestinal mucin secreting goblet cells are columnar cells exhibiting both secretory and absorptive utrastructures

Red velvety mucosa between smooth pale pink squamous mucosa or light brown gastric mucosa; definitive diagnosis if columnar mucosa contains intestinal goblet cells

white males between 40 and 60
Barrett esophagus
Patches of entire esophagus become covered by adherent gray-white pseudomembranes; densely matted fungal hyphae
esophagitis caused by candidiasis
punched out ulcers

immunohisochemical staining for virus provides diagnosis
esophagitis caused by herpesviruses
linear ulceration of the esophageal mucosa associated with a virus

usually in pt who are immunodeficient

immunohistochemical staining used to diagnose
esophagitis due to CMV
esophagitis with marked intimal proliferation iwth luminal narrowing

submucosa becomes severely fibrotic and mucosa exhibits atrophy, with flattening of the papillae
esophagitis following irradiation of the esophagus
mucosal polyps composed of combination of fibrous, vascular, or adipose tissue covered by intact mucosa
fibrovascular polyps/pedunculated lipoma

(benign)
benign tumor of smooth muscle cell origin
leiomyoma
sessile lesions with central core of connective tissue and hyperplastic papilliform squamous mucosa
squamous papilloma
papilloma associated with human papillomavirus
condyloma
benign tumor that resembles malignant lesion
inflammatory polyp/inflammatory pseudotumor
most common type of carcinoma in the esophagus

higher incidence in Iran, Central China, South Africa, and southern Brazil

Predominantly disease of males with higher risk for blacks than whites regardless of country of origin or current residence
squamous cell carcinoma
Increased epithelial cell turnover, which progresses to dysplasia

early lesions appear as small gray-white, plaque-like thickenings or elevations of the mucosa

Most are moderately to well differentiated
squamous cell carcinoma
squamous cell carcinoma that is a polypoid exophyti lesion that protrudes into the lumen
protruded
squamous cell carcinoma that is a diffuse, infiltrative form hat tends to spread within the wall of the esophagus

Causes thickness, rigidity, and narrowing of lumen
flat
squamous cell carcinoma characterized by necrotic cancerous ulceration that may erode the respiratory (fistula and pneumonia) or aorta

may permiate the mediastinum or pericardium
excavated
extensive circumferential and longitudinal spread

intramural tumor cell clusters may be seen near the main mass
squamous cell carcinoma
nodes squamous cell carcinomas of the upper third of the esophagus metastisize to
cervical lymph nodes
nodes sqamous cell carcinomas of the middle third of the esophagus metastisize to
paratracheal and tracheobronchial
nodes squamous cell carcinomas of the lower third of the esophagus spread to
gastric and celiac
Insidious onset that produces dysphagia and obstruction gradually and late

Progressively altered diet from solid to liquids

Extreme weight loss and debilitation

hemorrhage adn sepsis may accompany tumor ulceration
squamous cell carcinoma
Malignant epithelial tumor with glandular differentiation

Usually in lower third of esophagus

Majority of cases arise from Barret mucos or, rarely, heterotopic gastric mucosa or submucosal glands
adenocarcinoma of the esophagus
Tumor usually located in the distal esophagus and may invade adjacent gastric cardia

May develop into large nodular masses up to 5 cm in diameter or may exhibit diffusely infiltrative or deeply ulcerative features

Multiple foci of dysplastic mucosa are frequently adjacent to the tumor-> multisite biopsy
adenocarcinoma of the esophagus
Tumor more common in men than women and more common in whites than blacks

difficulty swallowing, progressive weight loss, bleeding, chest pain, and vomiting

Long-term symptoms of heartburn, regurgitation, and epigastric pain in less than half newly diagnosed patients
adenocarcinoma of the esophagus
defective absorption of fats, fat-soluble and other vitamins, proteins, carbohydrates, electrolytes and minerals, and water

chronic diarrhea, and steatorrhea
malabsorption
proteins, carbohydrates, and fats are broken down into assimible forms

begins in saliva and gets boost from gastric peptic digestion
intraluminal digestion
hydrolysis of carbohydrates and peptides by disaccharidases and peptidases in the brush border
terminal digestion
nutrients, fluid, and electrolytes are transported across epithelium of the small intestine for delivery to the intestinal vasculature
transepithelial transport
bulky, frothy, greasy, yellow, or gray stools

weight loss, anorexia, abdominal distention, borborygmi, and muscle wasting
malabsorption
chronic disease in which there is a characteristic mucosal lesion of teh small intestine and impaired nutrient absorptoin

improves with the withdrawal of wheat gliadins and related grains from the diet

occurs largely in caucasians
celiac disease
sensitivity to gluten

T-cell mediated chronic inflammatory reaction with an autoimmune component, which most likely develops as a consequence of a loss of tolerace to gluten

accumulation of intraepithelial CD8+ cells and large numbers of lamina propria CD4+ cells

small intestinal mucosa appears flat or scalloped
celiac disease
diffuse enteritis with marked atrophy or total loss of villi

crypts on the other hand, exhibit increased mitotic activity and are elongated, hyperplastic, and tortuous, so that the overall mucosal thickness is the same
celiac disease
symptomatic diarrhea, flatulence, weight loss, and fatigue

characteristic skin blistering lesion, dermatitis herpetiformis

anti-glandin or anti-endomysial antibodies
celiac disease
clinical documentation of malabsorption, demonstration of intestinal lesion by small bowel biopsy, unequivocal improvement in both symptoms and mucosal histology on gluten withdrawal diet

long term risk of malignant disease
celiac disease
celiac like disease that occurs almost exclusively in people living in or visiting the tropics

injury seen at all levels of the small intestine

Pt frequently have folate and/or vitamin B12 deficiency

mainstay treatment is antibiotic
triopical sprue
T. whippelii

small-intestinal mucosa laden with distended macrophages in the lamina propria

PAS positive, diastase-resistant granules and rod shaped bacilli

shaggy gross appearance to intestinal mucosal surface; edema thickens intestinal wall

bacilli laden macrophages found in the synovial membranes of affected joints, the brain, cardiac valves; inflammation is absent at these sites
whipple disease
caucasians in the fourth to fifth decades of life with male predominance

presents in form of malabsorption with diarrhea and weight loss, sometimes of years duration

arthropathy is often the initial

lymphadenopathy and hyperpigmentation present in over half of patients

response to antibotic therapy is usually prompt
whipple disease
enzymatic disease common among Native Americans and African Americans

incomplete breakdown of lactose-> osmotic diarrhea from unabsorbed lactose

bacterial fermentation of unabsorbed sugars leads to increased hydrogen production which can be measured in exhaled air by gas chromatography

in infants: explosive, watery, frothy stools and abdominal distension
lactase insuficiency
free fatty acids and monoglycerides that are produced by hydrolyssi of dietary fat enter the absorptive epithelial cells and are re-esterified normally but cannot assemble into chylomicrons

manifest in infancy: failure to thrive, diarrhea, and steatorrhea
abetalipoproteinemia
set of chronic inflammatory conditions resulting from inappropriate and persistent activation of teh mucosal immune system driven by the presence of normal intraluminal flora

individuals of Norther European descent
idiopathic inflammatory bowel disease
chronic inflammatory disease limited to the colon and rectum
ulcerative colitis
autoimmune disease that may affect any portion of the gastrointestinal tract from esophagus to anus, but most often involves the distal small intestine and colon
chrones disease
strong immune responses against norma flora

defects in epithelial barrier function of the GI
inflammatory bowel disease
NOD2 mutations

reduction in activity of the protein resulting in the persistence of intracellular microbes

uncontrolled, prolonged immune responses
crohn's disease
pANCA positive
more in UC than CD
elevation of S cervisiae antibody (ASCA)
crohn's disease
sharply delineated bowel segments diseased with intervening unaffected "skip" regions

any level of the alimentary tract may be involved

presence of noncaseating granulomas

fissuring with formation of fistulae

Primarily in western developed populations with peak presentation in 6th and 7th decades

slightly more prevelent in females; occurs 3-5x more often among Jews
crohn's disease
granular, gray serosa with mesenteric fat wraps around the bowel surface (creeping fat)

rubbery, thick intestinal wall due to edema, inflammation, fibrosis, and hypertrophy of muscularis propria

"string sign" on exray (thin stream of barium passing through diseased segment)

focal mucosal ulcers, loss of normal mucosal texure; coalesce into long, serpentine linear ulcers
crohn's disease
With advanced disease mucosa takes on textured, cobblestone appearance

bowel adhesions and serositis

eventual fistula or sinus tract formation either to adherent viscus, outside skin, or blind cavity
crohn's disease
focal neutrophilic infiltration into epithelial layer

infiltration of isolated crypts leadign to crypt abcess and destruction of crypt
crohn's disease
variable villus blunting

irregularity and branchign of crypts in the colon

pyloric/paneth cell metaplasia

chronic inflammatory cells in affected mucosa and underlying layers

lymphoid aggregates
crohn's disease
sarcoid-like granulomas may be present in all tissue layers, in both areas of active disease and "skip regions"

reduplication, thickening, and irregularity of muscularis mucosa-> eventual stricture formation
crohn's disease
disease usually begins with intermittent attacks of relatively mild diarrhea, fever, and abdominal pain; often attacks precipitated by periods of physical emotional stress

occult or overt fecal blood loss (massive bleeding uncommon)

acute right lower quadrant pain

fluid and electrolyte loss, weight loss, and weakness
crohn's disease
marked loss of albumin, generalized malabsorption, specific malabsorption of vitamin B12, or malabsorption of bile salts

steatorrhea

migratory polyarthritis, sacroilitis, ankylosing spondylitis, erythema nodosum, and clubbing of the fingertips
crohn's disease
hepatic primary sclerosing cholangitis
occurs in both UC and CD but association stronger with UC
ulceroinflammatory disease limited to the colon and affecting only the mucosa and submucosa except in severe cases

well formed granulomas are absent

migratory polyarthritis, sacroilitis, ankylosing spondylitis, uveitis, hepatic involvement, primary sclerosing cholangitis

more common amongst whites and males; onset peaks between 20 and 25
ulcerative colitis
inflammatory disease that involves rectum and extends in a retrograde fasion to involve the entire colon

slight reddening and granularity with friability and easy bleeding

extensive and broad based ulceration of the mucosa in the distal colon or throughout its length

pseudopolyps and tunnels covered by tenuous mucosal bridges

flattened and attenuated mucosal surface; serosal surface is usually normal
ulcerative colitis
inflammatory bowel disease with involvement of the appendix
both UC and CD
possible gangrenous toxic megacolon

inflammation, chronic mucosal damage and ulceration

diffuse, predominantly mononuclear inflammatory infiltrate in the lamina propria (crypt abcesses)

outright ulceration leading into the submucosa and sometimes leaving only the raw exposed muscularis propria

submucoasl fibrosis and mucosal architectural disarray and atrophy in healed disease
ulcerative colitis
ulcerative disease of the large bowel with no skip regions

strong risk for colorectal adenomas and carcinomas
ulcerative colitis
relapsing disorder marked by attacks of bloody mucoid diarrhea that may persist for days, weeks, with asymptomatic intervals following

bloody diarrhea containing stringy mucus accompanied by lower abdominal pain and cramps

first attack often preceeded by emotional/physical stress

perforation is potentially lethal event
ulcerative colitis
diarrheal illness

malabsorptive syndrome with small intestinal villus atrophy or colitic syndrome resembling UC

absence of demonstrable pathogens
AIDS patients
significant complication of bone marrow transplant

results from pretransplant conditioning that causes toxic injury to small intestinal mucosa

villus blunting, degeneration and flattening of crypt epithelial cells, decreased mitoses, atypia of cell nuclei

focal crypt necrosis

total sloughing of mucosa; possible sepsis and intestinal hemorrhage
graft versus host disease
complications of intestinal transplant
CMV infection and rejection
pill adhres to the mucosa and releases all of its contents locally

associated with "dry swallows"
focal ulceration
severe impairment of normal proliferative activity of small intestinal and colonic mucosal epithelium

anorexia, abdominal cramps, malabsorptive diarrhea

may be accompanied by ischemic fibrosis and stricture
radiation enterocolitis
severe acute adn chronic inflammation of the cecal and appendiceal region

impaired mucosal immunity in combination with compromised blood flow in the cecal region
neutropenic colitis (typhlitis)
inflammatory mucosal lesion occuring in segments of the colon that have been surgically isolated

caloric supply from short chain FA present in luminal stream-> surgical diversion of stream renders colonic mucosa susceptible to deprivation
diversion colitis
inflammaotry condition of rectum resulting from motor dysfunction of the anorectal musculature

dysregulation of anorectal sphincter; impaired relaxation of anorectal sling-> sharp angulation of anterior rectal shelf

inflammatory polyp

rectal bleeding, mucus discharge from anus, superficial ulceration of anterior rectal wall
solitary rectal ulcer syndrome