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;
90 Cards in this Set
- Front
- Back
Retroperitoneal structures
|
SADPUCKR
Suprarenal glands Aorta/IVC Duodenum Pancreas Ureters Colon, ascending and descending Kidney Rectum |
|
Falciform ligament
|
Liver --> anterior abdomen
Contains ligamentum teres Derived from fetal umbilical vein |
|
Hepatoduodenal ligament
|
Liver --> duodenum
Contains portal triad (hepatic a., portal v., common bile duct) Compress b/t thumb and finger in the epiploic foramen of Winslow |
|
Gastrohepatic ligament
|
Liver --> lesser curvature
Contains gastric arteries Cut during surgery when trying to access lesser sac |
|
Meissner's plexus
|
Submucosal
Regulate secretions |
|
Auerbach's plexus
|
Myenteric (muscularis externa)
Regulates motility |
|
Layers of GIT
Inside --> outside |
Mucosa (epithelium, lamina propria, muscularis mucosa)
Submucosa Muscularis externa (circular) Muscularis externa (longitudinal) Serosa |
|
Highest frequency slow waves in GIT
|
duodenum
|
|
Slowest frequency slow waves in the GIT
|
stomach
|
|
Foregut structures, artery, and nerve
|
Stomach to proximal duodenum, liver, gallbladder, pancreas
The spleen is not a foregut organ, but is supplied by celiac artery too Vagus innervation |
|
Midgut structures, artery, nerve
|
distal duodenum to transverse colon
SMA Vagus innervation |
|
Hindgut structures, artery, nerve
|
end of transverse colon to rectum
SPLENIC FLEXURE is a watershed region b/t SMA and IMA IMA pelvic innervation |
|
SMA syndrome
|
partial obstruction w/bilious vomiting due to transverse duodenum trapped b/t SMA and aorta
Seen in rapid weight loss, lordosis, bed rest |
|
3 sites of anastomoses in GIT
|
1. Esophagus (varices)
2. Umbilicus (caput medusae) 3. Rectum (internal hemorrhoids) |
|
Where can a portocaval shunt be placed to relieve portal HTN?
|
B/t splenic and left renal veins
|
|
Arterial supplies above and below pectinate line
|
Above: superior rectal a. (branch of IMA)
Below: inferior rectal a. (branch of internal pudendal a.) |
|
Why do external hemorrhoids hurt?
|
b/c of pudendal nerve (somatic) innervation (internal hemorrhoids = visceral innervation; no pain)
|
|
What zone of liver is most affected by viral hepatitis?
|
Zone 1
portal triad area |
|
What zone of liver is most affected by hypoxia, EtOH hepatitis, and contains p450
|
Zone 3
central vein area (--> hepatic vein, systemic circulation) |
|
What is unique about the basal surface of hepatocytes (face the sinusoids)?
|
No BM and fenestrated
allow plasma macromolecules to pass through perisinusoidal space (of Disse) |
|
Borders of the femoral triangle
|
Sartorius muscle
Adductor longus muscle Inguinal ligament |
|
In men and women, which does the inguinal canal contain?
|
Men: spermatic cord and cremasteric muscle
Women: round ligament In both, transmits the inguinal nerve |
|
Indirect hernia
Where? Why? |
Deep inguinal ring AND superficial inguinal ring, lateral to inferior epigastric a.
Into scrotum, covered by all 3 spermatic fascial layers Failure of processus vaginal to close (male infants) |
|
Direct hernia
|
Abdominal wall protrusion then through the superficial inguinal ring, medial to inferior epigastric a.
Covered by external spermatic fascia ONLY Old men bulge that decreases w/reclining |
|
What fascial layer defect is known as the deep/internal inguinal ring?
|
Transversalis fascia
|
|
What layer defect is known as the external/superficial inguinal ring?
|
External oblique
|
|
Hernia that protrudes below inguinal ligament through femoral canal
What is a complication? |
Femoral hernia
Women---leading cause of bowel incarceration!!! |
|
Hernia where GE junction is displaced
|
Sliding (very common)
|
|
Hernia where GE junction is normal, and just cardia moves into thorax
|
Paraesophageal
|
|
Where are Peyers patches found
|
lamina propria and submucosa of ILEUM
|
|
Gland that secretes the most serous saliva?
|
Parotid
|
|
Gland that secretes the most mucinous saliva?
|
sublingual
|
|
Where are Brunner's glands located and what do they do
When would you see hypertrophy of these glands? |
Secrete alkaline mucus to neutralize acid into crypts of Leiberkuhn
DUODENAL submucosa (the only GI submucosal glands) Hypertrophy in peptic ulcer disease |
|
"left-sided appendicitis" and bright red stools
|
diverticulitis (a complication of diverticulosis)
|
|
What systemic disease might small bowel diverticula suggest?
|
Sclerosis
|
|
True diverticulum
|
3 gut wall layers (mucosa, submucosa, and muscular layer) outpouch
|
|
False, "pseudo", diverticulum
|
only mucosa and submucosa outpouch, usually near a vessel (vasa recta) of the sigmoid colon
|
|
Zencker's diverticulum
Where? What Sx? |
false diverticulum
junction of pharynx and esophagus --> halitosis, dysphagia, obstruction |
|
Persistence of vitelline duct, or yolk stalk
|
Meckel's diverticulum
|
|
What is the rule of "five 2's" of Meckels diverticulum?
|
2 inches long
2 feet from iliocecal valve, in the ileum 2% of population 2 y/o presentation 2 types of tissues- ectopic H+ secreting gastric mucosa, and pancreatic tissue |
|
Omphalomesenteric cyst
|
cystic dilation of vitelline duct due to persistence of vitelline duct
|
|
Causes of bowel obstruction
|
#1- Adhesions
#2- Indirect inguinal hernia Chrone's Duodenal atresia |
|
What part of bowels does Hirschprung's affect?
|
Rectum
|
|
Necrosis of intestional mucosa, usually colon but can be anywhere
Who is most at risk and how do they present? |
nectrotizing enterocolitis
preemies w/dusky looking skin |
|
What is the main clinical diff. b/t adenomatous and villous polyps of the large intestine?
|
Adenomatous polyps are benign, and don't need to be removed
Villous adenomas are large w/high cancer risk and should be removed |
|
Where does ischemic colitis usually occur?
What is the most common cause? |
Splenic flexure
SMA atherosclerosis |
|
What do villous adenomas secrete?
|
Protein rich, K+ rich fluid
|
|
Left and ride sided colon cancer presentations
|
Left side: obstruction. Change in stool caliber, cramping, abdominal pain, N/V
Right side: bleeding. Iron-def. anemia, pallor, fatigue They both present anorexia, weight loss, and malaise |
|
What is a guaiac test?
|
Hb or Mb reacts w/peroxidase and oxidation creates a color change
|
|
Dx of colon cancer...
|
Apple core barium scan
CEA (+) |
|
Sequence of events in FAP that leads to cancer:
|
1. APC tumor suppressor gene (chrom. 5) mutation
2. K-RAS mutation leads to unregulated growth of polyp 3. Malignant transformation w/p53 and DCC gene mutation |
|
APC w/brain involvement
|
Turcot's syndrome
|
|
APC w/osseous and soft tissue tumors, retinal hyperplasia
|
Gardner's syndrome
|
|
Hamartomoutous colon AND SMALL INTESTINE polyps, hyperpigmented mucosal surfaces and hands
|
Putz-Jeghers syndrome
|
|
Serotonin syndrome
|
Rapid onset tachycardia, hyperthermia, HTN, sweating, miosis, myoclonus, and hyperreflexia
|
|
Small intestine tumor of endocrine cells that appear as "dense core bodies' on EM
|
carcinoid tumor
|
|
Testing peritoneal fluid for ascites of liver of peritoneal fluid
|
Serum albumin/fluid albumin
>1.1 is liver ascites (transudate) <1.1 is exudate |
|
What are the effects of hyperestrinism in liver cirrhosis
|
gynecomastia
spinder telangioectasias testicular atrophy palmar erythema |
|
What are the Sx of encephalopathy in cirrhosis?
|
Mental status changes
Flapping asterixis Coma |
|
There are two types of shunts used in cirrhosis, one decreases risk of encephalopathy and one relieves portal HTN
|
1. transjugular intrahepatic portosystemic shunt (TIPS)
2. portacaval shunt b/t splenic vein and left renal vein |
|
Marker of p450 induction
|
GGT
|
|
Microvesicular fatty change
|
Reye's syndrome
Also see encephalopathy and increased transaminases |
|
Macrovesicular fatty change
|
hepatic steatosis (reversible) due to alcoholic liver disease
|
|
What liver disease would you see very low transaminases, hyperammonemia?
|
Fulminant liver failure
|
|
Risk factors for hepatocellular carcinoma
|
HepB/C
Wilson's disease Hemochromatosis AAT deficiency Alcoholic cirrhosis Carcinogens (aflatoxins) |
|
Marker for hepatocellular carcinoma
|
alpha-FP
|
|
Budd-Chiari and RSHF cause this liver appearance
|
Nutmeg liver (congestion); decreased outflow
|
|
Occlusion of IVC or hepatic veins, leading to congestive liver failure WITHOUT JVD
|
Budd-Chiari
|
|
"red cytoplasmic granules" in liver on PAS stain
|
AAT deficiency, misfolded gene that accumulates in children w/cirrhosis
|
|
Difference in cell infiltration of alcoholic and viral hepatitis
|
Alcoholic- neutrophils
Viral- lymphs |
|
Gilbert's syndrome
|
decreased UDP-glucoronyl transferase
Benign |
|
Crigler-Najjar type I
|
Absent UDP-glucoronyl transferase
Kernicterus |
|
How do you treat Crigler-Najjar type II
|
Phenobarbital
|
|
Dubin-Johnson syndrome
|
Conjugated bilirubin accumulation due to defective liver exretion
Benign, but grossly black liver **Epi metabolites in hepatocytes |
|
Jaundice in newborns due to inflammatory destruction of bile ducts
Need a liver transplant |
Extrahepatic biliary atresia
|
|
What causes micronodular cirrhosis?
|
Alcohol and hemochromatosis
|
|
Bronze diabetes and skin pigmentations
|
Hemochromatosis
|
|
Inflammation and fibrosis of bile ducts --> strictures and dilations w/beading on ERCP
|
Primary sclerosing cholangitis
assc. w/UC, and can lead to secondary biliary cirhhosis |
|
Primary vs. secondary biliary cirrhosis (location)
|
Primary: intrahepatic, AI disorder (serum anti-mitochondrial ABs). Assc. w/scleroderma
Secondary: extrahepatic biliary obstruction (PSC, CF) Both have increased ALP, pruritis, jaundice, hepatosplnomegaly, xanthalesma |
|
the 4 F's of cholesterol stones
|
Fat
Female Fertile Forty |
|
Ascending cholangitis
|
Bacterial inflammation of bile duct
Increased ALP |
|
Causes of acute pancreatitis
|
Gallstones
EtOH Trauma (in kids, seatbelt injury) Steroids Mumps AI disease Scorpion sting Hypercalcemia/hyperlipidemia Sulfa drugs |
|
Gold standard Dx acute pancreatitis
|
Contrast CT
|
|
Enzymatic fat necrosis
|
Unique to acute pancreatitis
Lipase released by pancreas degrades TGs --> FA (saponification), then Ca++ calcifies it into chalky substance (dystrophic calcification) |
|
Chronic pancreatitis
|
Pancreatic insufficiency --> malabsorption and DM
"chain of lakes" on ERCP from dilations of pancreatic ducts If calcifying chronic pancreatitis, strong assc. w/alcoholism |
|
Marker for pancreatic adenocarcinoma
|
CA-19-9
|
|
Pancreas disease presents in what way?
|
Pain radiating to back, weight loss, obstructive jaundice
|
|
"C-sign" of pancreas in adenocarcinoma
|
Where pancreatic head indents teh duodenum
|
|
Whipple's procedure
|
pancreaoduodenalectomy
take out 1/2 stomach, 1/2 duodenum, and whole pancreas |
|
What compound is used to test brush border enzymes independent of pancreatic function?
|
D-xylolose; b/c it is already a monosaccharide and doesn't depend on amylase from pancreas for absorption
|