GI Flashcards

(160 cards)

1
Q

Most common location of salivary gland tumors:

A

Parotid gland

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2
Q

Most common salivary gland tumor:

Second most common:

A

Pleomorphic adenoma

Warthin’s tumor

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3
Q

Most common malignant salivary gland tumor:

A

Mucoepidermoid carcinoma

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4
Q

This very common genetic defect is a risk for duodenal atresia:

A

Trisomy 21

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5
Q

Jejunal, ileal, and colonic atresia are due to this event during fetal development. What about duodenal atresia?

A

Duodenal = failure to recanalize

Jejunal et c = vascular accident

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6
Q

This anterior abdominal wall defect can contain a herniated liver, whereas this does not.

A

Omphalocele can have the liver protruding

Gastroschisis does not

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7
Q

These structures are retroperitoneal (9):

A
A DUCK PEAR:
Adrenals
Duodenoum
Ureters
Colon (descending and ascending)
Kidneys
Pancreas (except tail)
Esophagus
Aorta / IVC
Rectum
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8
Q

Three metabolic abnormalities that may be seen in an infant with pyloric stenosis:

A

Hypochloremia
Metabolic alkalosis
Hypokalemia (K+ shift into cells to allow H+ out into blood)

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9
Q

Pale clay colored stool, tea urine, jaundice in the first weeks of life:

A

Extrahepatic biliary stenosis, failure of the bile ducts to completely re-canalize.

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10
Q

The pancreas is derived from this embryonic structure:

A

Foregut

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11
Q

Which pancreatic bud contributes to the head and main pancreatic duct?

A

Ventral bud

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12
Q

How does an annular pancreas happen?

A

Ventral bud is in two pieces

Dorsal / ventral fuse abnormally and encircle the duodenum.

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13
Q

Where does the spleen come from? From what tissue layer is it derived?

A

The stomach mesentary, it’s mesodermal.

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14
Q

What structures come from the hepatic diverticulum off the ventral foregut?

A

Liver
Gall bladder / biliary tree
Ventral pancreatic bud

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15
Q

Which pancreatic bud travels to meet the other bud?

A

Ventral swings around dorsally to join the dorsal pancreatic bud.

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16
Q

This embryonic structure gives rise to the body, tail, and isthmus of the pancreas:

A

Dorsal pancreatic bud

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17
Q

This ligament contains the portal triad:

A

Hepatoduodenal

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18
Q

Access to the lesser sac through this ligament:

A

Gastrohepatic

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19
Q

The tail of the pancreas is embedded in this ligament:

A

Splenorenal

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20
Q

The gastric arteries are in this ligament:

A

Gastrohepatic

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21
Q

This ligament is the remnant of the fetal umbilical vein:

A

Ligamentum teres hepatis

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22
Q

What are the layers of the gut wall (inside out) (4)?

A

Mucosa
Submucosa
Muscularis externa
Serosa / adventitia

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23
Q

This type of injury extends into the submucosa:

A

Ulceration

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24
Q

Where is the myenteric nerve plexus? What is its other name?

A

Myenteric = Auerbach’s

It is the OUTERbach’s plexus

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25
This nerve plexus is the inner nerve plexus and is located in the _________.
Submucosal nerve plexus is the inner one, aka Meissner's, it's in the submucosa, of course.
26
Three arteries to the GI structures come off the aorta anteriorly:
Celiac Superior mesenteric Inferior mesenteric
27
What is SMA syndrome?
The duodenum gets caught between the SMA and the aorta and is obstructed.
28
Parasympathetic innervation for the: Foregut Midgut Hindgut
Foregut and midgut = vagus | Hindgut = pelvic
29
The artery that supplies the foregut:
Celiac
30
The three main branches off the celiac trunk:
Common hepatic Splenic Left gastric
31
The common hepatic artery gives rise to three arteries, what are they?
Gastroduodenal Right gastric Hepatic artery proper
32
This artery gives rise to the main arteries to the pancreas:
Gastroduodenal via the anterior superior pancreaticoduodenal arteries
33
The R gastroepiploic artery comes from this origin, and the left comes from a separate vessel:
R from the gastroduodenal (off common hepatic) | L from the splenic (off celiac trunk)
34
Which zone in the liver is affected first by viral hepatitis?
Zone 1 = zone closest to the portal triad
35
Zone III is located near what structure in the liver?
Pericentral / centrilobular veins
36
What direction does bile flow relative to the central hepatic vein?
Away from it, toward the triad.
37
This hormone causes gall-bladder contraction:
CCK
38
What is the most common kind of stomach hernia? The most dangerous?
Sliding hiatal = most common | Paraesophageal = most dangerous, fundus can get trapped in this one.
39
Where do an indirect and a direct inguinal hernia lie relative to the inferior epigastric artery?
``` Indirect = lateral Direct = medial ```
40
Gastrin comes from these cells:
G cells
41
Pro-duodenal hormone:
CCK | This hormone is anti-gastrin
42
These two hormones are the main off-switch for gastric acid secretion:
CCK Secretin Somatostatin
43
Where is secretin made?
S cells in the duodenum
44
This hormone is the anti-hormone-hormone:
Somatostatin
45
This hormone hits parasympathetic ganglia in the gut:
VIP = vasoactive intestinal peptide
46
This substance helps relax the LES:
NO
47
This hormone is seriously elevated in Zollinger-Ellison syndrome:
Gastrin
48
Three common substances that are potent stimulators of gastrin:
Calcium Phenylalanine Tryptophan
49
Three histologic / gross / lab findings in a stomach of someone with ZE syndrome:
Thick rugae High gastrin Glandular hyperplasia
50
Cells that make IF:
Parietal cells
51
These glands in the duodenal submucosa secrete alkaline mucus: When might they be hypertrophied?
Brunner's | Peptic ulcer disease
52
Gastrin increases acid secretion indirectly. Briefly explain how this happens:
Gastrin hits ECL cells in the gut, which release histamine; it is histamine that hits parietal cells and tells them to secrete acid.
53
Type of receptor on parietal cells most important for stimulating acid secretion:
H2
54
Two Gi coupled receptors on a parietal cell:
Prostoglandin Somatostatin Both inhibit acid secretion
55
The H2 receptor on a parietal cell works through what second messenger?
cAMP
56
Two hormones stimulate pancreatic secretions:
CCK | Secretin
57
Where are oligosaccharide hydrolases located?
At the brush border of the intestines.
58
What is the rate-limiting step in carbohydrate digestion?
Monosaccharide production by oligosaccharide hydrolases
59
This sugar transporter sends both glucose and fructose from an enterocyte into the blood:
GLUT2
60
Glucose and galactose enter an enterocyte on this transporter: What kind of carrier is it?
SGLT-1 | Na-dependent
61
How is fructose taken into an enterocyte?
Facilitated diffusion through GLUT-5
62
What is the plasma carrier protein for vitamin B12?
Transcobalamin
63
Where are each of the following vitamins absorbed? Iron, Folate, B12:
Iron: Duodenum Folate: Jejunum B12: Terminal ileum, needs IF
64
The cells in Peyer's patches that take up antigen:
M cells
65
Where do B cells in the gut live?
In Peyer's patches, inside the lamina propria
66
What enzyme catalyzes the rate-limiting step for bile salt formation?
Cholesterol 7a-hydroxylase
67
Which form of bilirubin is water-soluble -- direct or indirect?
Direct = conjugated = water soluble.
68
Gut bacteria convert conjugated bilirubin into this molecule, which either goes out into the feces as stercobilin or gets resorbed via the mesenteric veins and sent to the kidney / liver:
Urobilinogen
69
This salivary gland tumor has germinal centers:
Warthin's tumor = papillary cystadenoma lymphomatosum
70
This salivary tumor has mucinous and squamous parts. It is the second most common tumor overall:
Mucoepidermoid carcinoma
71
Most tumors in this gland are malignant:
Sublingual
72
What does a Warthin's tumor look like?
A lymph node: Columnar epithelium on a wad of lymph cells with a little stroma
73
Loss of innervation to this plexus leads to achalasia:
Auerbach's (myenteric)
74
T/F: Achalasia increases the risk of squamous cell carcinoma:
T.
75
Primary achalasia has a high LES opening pressure. This disorder involves a low pressure proximal to the LES:
CREST / Scleroderma
76
This infection can give rise to secondary achalasia:
Chagas (=Trypanosoma cruzii)
77
CMV esophagitis looks like:
CMV: Linear ulcers, large cells with clear perinuclear halo.
78
HSV esophagitis looks like:
Punched-out ulcers, large pink nuclear inclusions.
79
What is Whipple's disease?
Infection with Tropheryma whipplei (gram + organism). Leads to malabsorption.
80
Features of Whipple's disease (5):
``` WHIPped cream in a CAN: Cardiac sx Arthralgias Neurologic sx FOAMY macrophages in intestinal mucosa Lymphadenopathy ```
81
Malabsorption, neurologic manifestations, autosomal recessive, acanthocytes:
Abetalipoproteinemia
82
HLA associated with Celiac:
HLA-DQ2, DQ8
83
Three Ab you can find in Celiac disease:
Anti-endomysial Anti-gliaden Anti-tissue transglutaminase
84
Acute erosive gastritis, 3 features:
Neutrophils Loss of surface epithelium Purulent exudate with fibrin
85
Chronic gastritis, 2 features:
Lymphoid aggregates | Atrophied glands
86
Two injuries that can cause acute erosive gastritis:
Burns (Curling ulcer) | TBI (Cushing ulcer)
87
Type A gastritis: autoimmune or caused by H. pylori? Location in the stomach?
Autoimmune. AutoAb, Anemia (pernicious), Achlorhydria In the body of the stomach
88
H. pylori infection causes this type of gastritis:
Chronic, non-erosive, type B (in the antrum)
89
What is Menetrier's disease?
Gastric hypertrophy with huge increase in mucous cells. Patients have protein loss sufficeint to cause hypoalbuminemia.
90
Super hypertrophied rugae:
Menetrier's disease
91
Krukenberg's tumor, what is it?
Bilateral metastasis of stomach cancer to ovaries. See mucus, signet ring cells.
92
Three places you might see signet ring cells:
Lobular adenocarcinoma in situ (breast) Gastric cancer Kruckeberg's tumor of the ovary
93
This kind of ulcer will be accompanied by hypertrophy of Brunner's glands:
Duodenal ulcers
94
What is involved in triple therapy for H. pylori? | Quadruple therapy?
PPI + clarithromycin + amox or metronidazole | PPI + bismuth + metro + tetracycline
95
Tx for irritable bowel syndrome (5):
``` Fiber TCAs SSRIs Loperamide Alosetron ```
96
Where do false diverticula commonly occur?
Most common in the sigmoid colon, where the vasa recta perforate the muscularis externa.
97
Three diverticula above the lower esophageal sphincter:
``` Zencker = above the UES Traction = mid-esophageal Epiphrenic = above the LES ```
98
Persistence of the vitelline duct, melena.
Meckel's diverticulum
99
Intussusception is most common at this location:
Ileocecal junction
100
"Double bubble" on X-ray:
Duodenal atresia
101
Pneumatosis intestinalis in a premie:
Necrotizing enterocolitis
102
Abdominal pain out of proportion to physical findings in an elderly person:
Ischemic colitis
103
Most common sites for angiodysplasia (3):
Cecum, terminal ileum, ascending colon
104
Carcinoid syndrome, 3 associated findings:
Bronchospasm Flushing Diarrhea Right sided heart disease / murmur
105
Most common sites for carcinoid tumors (3):
Appendix, ileum, rectum
106
Neurotransmitter leading to carcinoid syndrome:
5-HT
107
T/F: If a carcinoid tumor is confined to the GI tract, you will not see carcinoid syndrome.
T. Liver metabolizes 5-HT. Only mets outside the GI system will cause carcinoid syndrome.
108
Treatment for carcinoid syndrome:
Octreotide, somatostatin, find it and cut it out
109
This enzyme is elevated in the serum in mumps infection:
Amylase
110
Cause of Reye's syndrome:
Hepatoencephalopathy 2/2 mitochondrial damage in the liver caused by aspirin + viral infection in children
111
Two viruses especially linked to Reye's syndrome:
VZV, influenza B
112
Mallory bodies:
Alcoholic hepatitis
113
Does ethanol deplete ALT or AST?
ALT. This is the reason why AST > ALT in chronic alcoholic hepatitis.
114
What is the serum albumin ascites gradient? What does it mean to have a value >1.1?
SAAG = albumin in serum - albumin in ascites fluid. >1.1 cause is portal HTN, heart failure, Budd-Chiari.
115
A very common cause of GI bleeding among the elderly (excluding colon CA and diverticuar bleeds...):
Angiodysplasia
116
Most common cause of appendicitis in children: | In adults:
``` Children = lymphoid hyperplasia Adults = fecalith ```
117
Hirschprung's disease always involves this segment of the GI tract:
Rectum
118
Down syndrome patients are at risk for these GI problems (4):
Duodenal atresia Hirschprung Celiac Annular pancreas
119
Angiodysplasia is most common in the [3]:
Cecum, terminal ileum, ascending colon
120
Type of colon polyp with greatest malignant potential:
Villous adenoma | VILlous VILlain
121
This type of polyp is not a risk for CRC:
Hyperplastic
122
Non-malignant hamartomas, hyperpigmented lips, mouth, genitalia:
Peutz-Jeghers
123
Peutz-Jeghers is associated with cancer, can you name six?
``` CRC pancreatic small intestinal stomach breast uterine ```
124
Three big-name genes in CRC:
APC K-RAS p53
125
FAP with osseous and soft tissue tumors:
Gardner's syndrome
126
FAP with a CNS tumor:
Turcot's syndrome TURcot's TURban Usually a medulloblastoma
127
Lynch syndrome is caused by this defect:
DNA mis-match repair
128
Cancer in the most proximal colon is most commonly caused by:
HNPCC = Lynch syndrome
129
Good marker for colon CA recurrence:
CEA
130
Order of gene events for CRC genesis:
APC K-RAS p53 AK-53
131
Carcinoid syndrome is caused by excess of this neurotransmitter:
5-HT
132
Medical treatment for carcinoid syndrome:
Octreotide / somatostatin
133
Tumor of neuroendocrine cells in the appendix might be likely to cause these symptoms:
``` Carcinoid syndrome, B-FDR: Bronchospasm (wheezing) Flushing Diarrhea R sided heart murmur ```
134
Carcinoid syndrome can be observed with a tumor in the GI tract. Explain how this happens:
Tumor must have mets to the liver. Liver otherwise metabolizes 5-HT and you do not see carcinoid syndrome from GI-confined cancers.
135
Inflammatory bowel disease with skip lesions and rectal sparing:
Chron's
136
Inflammatory bowel disease associated with primary sclerosing cholangitis:
UC
137
Inflammatory bowel disease with rectal involvement:
UC
138
Microscopic morphology of Chron's colon: | Of UC:
``` Chrons = noncaseating gramulomas, lymphoid aggregates UC = Crypt abscesses and ulcers, bleeding ```
139
Cell response mediating disease process in: Chron's UC
``` Chron's = Th1 UC = Th2 ```
140
Gross morphology of Chron's colon (2 core features):
Cobblestoned, transmural thickening
141
Gross morphology of a colon in UC (3 features):
Inflammation is mucosal and sub-mucosal Friable pseudopolyps Loss of haustra (lead pipe appearance)
142
Embryonic source of tissue above the pectinate line: | Below the pectinate line:
Endoderm | Ectoderm
143
Painful hemorrhoids:
External hemorrhoids
144
Represents greatest risk for developing squamous cell CA in the anal region:
HPV 16, 18, 31
145
The inferior rectal artery is a branch of:
The internal pudendal
146
LLQ pain and bleeding:
Diverticulitis
147
Treatment for diverticulitis:
Metronidazole (covers anaerobes) + | TMP-SMX or Levo or Cipro
148
This virus is associated with intussusception:
Adenovirus
149
5-ASA agents (2): | These are used in treatment of?
Mesalazine Sulfasalazine Chron's and UC
150
Most likely underlying cause of gallstones in a patient with Chron's:
Bile acid wasting | Terminal ileum usually resorbs, damage to mucosa = less bile acid with more cholesterol = stones
151
Abdominal discomfort, joint pain, greasy stool, weight loss, macrophages with PAS+ granules in the lamina propria:
Whipple disease = Tropheryma whippelii
152
Small intestine mucosa contains PAS+ diestase-resistant granules, macrophages with rod-shaped bacilli:
Whipple disease
153
Red-violet, flat, macopapular lesions with hemorrhagic nodules on colonoscopy:
Kaposi's sarcoma
154
Basophilic clusters on surface of intestinal mucosal cells:
Cryptosporidium
155
Trophozoites containing RBCs:
Entamoeba histolytica
156
H. pylori most highly colonizes this part of the stomach:
Antrum | Pre-pyloric area
157
Peri-anal fistula: More characteristic of Chron's or UC?
Chron's
158
Location of the following ulcers: Cushing Curling Which are more prone to rupture?
Cushing = esophagus, stomach, or duodenum Curling = proximal duodenum Cushing are more prone to rupture (think increased ICP, more likely to pop)
159
What is the definition of an erosion? | An ulcer?
``` Erosion = loss of tissue that does not fully extend through the muscularis mucosa Ulcer = damage extending into the submucosa and beyond. ```
160
Chron's disease may be linked to activity of NF-kB. What is this protein responsible for?
Chron's = possible NOD2 defect, turns NF-kB on. NF-kB induces cytokine production.