GI Pathology Flashcards
characteristics pancreas
transversely oriented
retroperitoneal
main pancreatic duct
most commonly drains duodenum at papilla of Vater
accessory pancreatic duct
drains into duodenum minor papilla 2cm proximal to Vater
acinar cells
produce enzymes for digestion
pyramidally shaped
oriented radially around lumen
contain membrane bound zymogen granules with enzymes
agenesis
total-incompatible with life
homozygous PDX1 mutation on ch 13
pancreatic divisum
failure of fusion of fetal duct system of dorsal and ventral pancreatic primorida
bulk through small caliber minor papilla
stenosis through minor papillae-leads to chronic pancreatitis
annular pancreas
band like ring encircles second part of duodenum
may present as duodenal obstruction
ectopic pancreas
stomach and duodenum common sites
can be associated with neoplasms
reversible inflammatory process
acute pancreatitis
irreversible loss of exocrine and endocrine function
chronic pancreatitis
biliary tract disease
females
alcoholism
males
causes of acute pancreatitis
gallstones, alcohol, trauma, steroids, mumps, autoimmune, scorpion, hyperlipidemia, drugs
clinical presentation acute pancreatitis
epigastric pain radiating to back
elevated amylase and lipase
cationic trypsinogen gene
AD PRSS1
trypsin resistant to cleavage and can lead to activation of other proenzymes
serine protease inhibitor Kazal 1
SPINK1
inhibits trypsin activity
AR
morphology acute pancreatitis
microvascular leakage-edema
necrosis of fat
acute inflammation
proteolytic destruction of pancreatic parenchyma
destruction of blood vessels and subsequent interstitial hemorrhage
causes of duct obstruction
gallstones and chronic alcoholism
causes of acinar cell injury
alcohol, drugs, trauma, ischemia, viruses
causes of defective intracellular transport
alcohol
trypsin and kinin
can activate clotting and complement cascade
poor prognostic sign acute pancreatitis
low calcium
Ranson criteria
predict severity of disease
cant be completed until 48 hrs
medical emergency pancreatitis
severe with necrosis
sequelae acute pancreatitis
increased WBC
hemolysis
ARDS
shock and death from peripheral vascular collapse
gross chronic pancreatitis
hard gland with calcific concretions
pseudocyst common
microscopic chronic pancreatitis
fibrosis
initially spares islets
US and CT chronic pancreatitis
calcification, ductal dilation, small cysts
clinical features chronic pancreatitis
mild fever
mild elevation serum amylase
weight loss
hypoalbuminemic anemia
congenital cysts
often coexist with polycystic disease
AD PCKD and VHL
pseudocyst
develops after inflammation
no epithelial lining
treatment pseudocyst
supportive care
surgical drainage
excellent prognosis
serous cystadenoma
lined by cuboidal, female in 70s
benign
mucinous cystic neoplasm
can have invasive carcinoma
involves body or tail
histology mucinous cystic neoplasm
lined by columnar and have ovarian like stroma
intraductal papillary mucinous neoplasm
males, can be malignant
in head and involves large pancreatic duct
solid pseudopapillary neoplasm
low grade in young women
solid and cystic filled with hemorrhagic debris
pancreatic carcinoma
adenocarcinoma more common in blacks
strongest link to smoking
mutations pancreatic adenocarcinoma
KRAS and p53
hereditary breast and ovarian cancer
BRCA2
familial atypical multiple mole melanoma syndrome
p16/CDKN2A
Peutz Jeghers syndrome
LKB1
clinical presentation pancreatic adenocarcinoma
most involve head and obstruct bile flow
painless jaundice
gross pancreatic adenocarcinoma
hard, stellate
gray-white, poorly defined mass
Trousseau’s sign
migratory thrombophlebitis
tumor produces platelet aggregating factors
acinar cell carcinoma
lipases cause metastatic fact necrosis
pancreatoblastoma
found ind children, malignant
micro acinar cells with squamoid differentiation
locations esophagus
from cricopharyngeal muscle to GE junction at T11/T12
areas of high pressure at rest
at cricopharyngeal muscles and lower esophageal sphincter
responsible for tone of LES
gastrin, Ach, serotonin
Z line
irregular serrated junction between squamous and columnar mucosa in distal esophagus
proximal to muscular GE by 2-3 cm
association congenital esophagus problems
heart disease
clinical presentation TE fistula
regurg on attempt to feed
complications TE fistula
aspiration and pneumonia
most common TE fistula
type C
upper blind pouch and lower connected to trachea
late complications TE fistula
GERD and esophagitis
ectopic gastric tissue
usually postcricoid
circular, red-orange flat area
micro gastric ectopic tissue
resembles cardiac-fundic glands
inflammation
ectopic pancreatic tissue
at GE junction most commonly
esophageal webs
protrusion of mucosa into lumen
covered by squamous mucosa and vascularized fibrous tissue core
causes esophageal webs
idiopathic in most
can be after radiation or GVHD
Schatzki ring
in lower esophagus (above squamocolumnar junction)
gastric epithelium on underside
stenosis
fibrous thickening especially submucosa
epithelium thin
causes stenosis
inflammation and scarring
reflux, radiation, scleroderma, lye ingestion
clinical stenosis
progressive dysphagia
achalasia
lack of progressive peristalsis due to increased LES resting tone
cause of achalasia
T cell mediated destruction or complete absence of myenteric ganglion cells
also could be from Chagas, polio, diabetic autonomic neuropathy, tumor, amyloidosis, sarcoidosis
treatment achalasia
esophagomyotomy and dilation
complications achalasia
increased risk of Candida, diverticula, aspiration, GERD, PUD, stricture and rupture
early histology achalasia
lymphocytic inflammation
cytotoxic T cells and eosinophils
late histology achalasia
collagen with muscular hypertrophy replacing ganglion cells
squamous mucosa hyperplastic with increased CD3
pseudoachalasia
associated with neoplasm (adenocarcinoma at GE junction)
hiatal hernia
separation of diaphragmatic crura and widening of space between muscular crura and esophageal wall
sliding hiatal hernia
bell shaped dilation
nonaxial (paraesophageal)
along grater curvature enters throax through widened foramen
accentuated GERD with hiatal hernia
bending forward, lying supine, obesity
complications hiatal hernia
ulceration, bleeding, perforation
strangulation of paraesophageal hernias
Mallory-Weiss tear
longitudinal tears at GE junction or in proximal gastric mucosa from vomiting
can be mucosal or full thickness
treatment Mallory-Weiss tear
support, vasoconstrictors, transfusions, balloon tamponade
Boerhaave syndrome
esophageal rupture
esophageal diverticula
out pouching of alimentary tract containing all visceral layers
epiphrenic diverticula
immediately above LES
due to lack of coordination of peristalsis and relaxation
contains mucosa, submucosa, and muscularis mucosa
mid-esophageal diverticula
may be due to TB, mediastinal lymphadenitis and scarring
Zenker’s diverticula
above upper esophageal sphincter due to disordered cricopharyngeal motor dysfunction or weakness in wall
neck mass
esophageal varices
dilated tortuous vessels (submucosal) due to formation of collaterals between portal and caval systems from prolonged HTN
associated with alcoholics
flow of collaterals esophageal varices
from portal vein into esophageal into azygous into vena cava
common cause of bleeding varices
hepatic schistosomiasis
treatment esophageal varices
sclerotherapy (injection of thrombotic agents)
balloon tamponade
causes of GERD
reflux of gastric contents, most common cause of esophagitis
central nervous system depressants, hypothyroidism, pregnancy, systemic sclerosing disorders, alcohol, tobacco, NG tube, sliding hiatal hernia
consequences of GERD
bleeding, stricture, Barrett’s esophagus
diagnosis GERD
intraesophageal pH monitoring
endoscopic and histologic examination
gross GERD appearance
hyperemic mucosa with focal hemorhage
micro GERD appearance
inflammatory cells in epithelial layer (eosinophils, neutrophils, T lymphocytes)
basal cell hyperplasia
elongation of lamina propria papillae into upper 1/3 of epithelium
importance of neutrophils in GERD micro
indicates more severe injury including ulceration and erosion
causes of carditis
h pylori gastritis and GERD
Barrett’s esophagus
replace with columnar epithelium due to chronic GERD
intestinal metaplasia
long segment Barrett’s esophagus
3cm or more from GE junction
short segment Barrett’s esophagus
less than 3cm from GE junction
treatment Barrett’s esophagus
anti-reflux therapy
endoscopy ever 1-2 years to detect dysplasia
gross appearance Barrett’s esophagus
velvety GI mucosa
tongues extending up from GE junction
micro Barrett’s esophagus
squamous replaced by columnar with intestinal types of epithelium with goblet cells
can also have fibrotic lamina propria
dysplasia
does not invade the lamina propria
risk of low grade dysplasia
high risk if >2cm
eosinophilic esophagitis
common in adults and has been increasing
allergic esophagitis
does not demonstrate acid in esophagus and does not respond to anti-reflux therapy
micro allergic esophagitis
eosinophils in larger numbers
causes of chemical esophagitis
strong alkalis, acids or nonphosphate detergents
cytotoxic chemotherapy
micro chemical esophagitis
mucosal or transmural injury with hemorrhage, necrosis and bacterial infection
when to consider infection for esophagitis
ulcer or exudate present
especially in immunocompromised patient
Candida
requires invasion-presence of pseudohyphae
endoscopy candida
gray-white pseudomembrane or plaques
micro candida
pseudohyphae in squamous debris
positive stain for PAS and GMS
gross CMV
punched out mucosal ulcers similar to herpes simplex
micro CMV
virus in endothelium
inclusions are intranuclear with clear halo
macrophage aggregates in perivascular distribution
inclusions NOT seen in squamous epithelial cells
gross HSV
shallow vesicles and ulcers
micro HSV
viral inclusions in multinucleated squamous cells
Cowdry A-eosinophilic and intracellular
macrophages adjacent to inflamed epithelium
other causes of esophagitis
irradiation pill-induced chemotherapy prolonged intubation uremia
mets esophgeal carcinoma
liver, lungs, pleura
causes squamous cell carcinoma
deficiency of vitamin A, C, thiamine, B6, riboflavin, zinc, molybdenum
fungal, nitrates, Betel nuts, alcohol, tobacco
mets squamous cell carcinoma
lungs, liver, bones, adrenal galnds
most important prognostic factor squamous cell
stage
gross squamous cell
most are protruded polypoid, exophytic
micro squamous cell
tumors cluster due to lymphatic spread through submucosa
focal glandular or small cell differentiation
adenocarcinoma
Barrett
most present after invasion through wall and nodal involvement
prognostic factors adenocarcinoma
depth of invasion, lymph node mets, status of resection margins
gross adenocarcinoma
distal esophagus
flat patches to nodular masses
micro adenocarcinoma
mucin producing
intestinal type mucosa
granular cell tumor
neural, may be Schwannian origin
intramural nodes
micro granular cell tumor
uniform cells with abundant eosinophilic granular cytoplasm and small nuceli
most common benign tumor of esophagus
leiomyoma
gross leiomyoma
bulges into lumen
whorled cut surface
micro leiomyoma
intersecting fascicles of bland spindle cells with variable fibrosis
heterotopic pancreas in stomach
nodules up to 1 cm in gastric or intestinal wall
usually antrum or pylorus
gross appearance heterotopic pancreas
nipple-like projection with duct emptying into gastric lumen
symmetric cone or round mass
pyloric stenosis
associated with Turner’s syndrome, trisomy 18, and esophageal atresia
symptoms pyloric stenosis
projectile non-billious vomiting in second week of life