GI 6 Flashcards

(71 cards)

1
Q

Describe the epidemiology of colorectal cancer (CRC)

A

1) 3rd most common diagnosed cancer worldwide
2) 2nd leading cause of malignancy-related death worldwide
3) Incidence & mortality decreasing (in U.S.)
5-year survival 64% (U.S.)

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2
Q

What are the risk factors for CRC?

A

Smoking, heavy alcohol intake
Consumption of red & processed meats, high fat diet
Diabetes mellitus
Physical inactivity
Obesity
History of IBD
Family history of GI neoplasia (CRC or adenomatous polyps) in first degree relative

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3
Q

Who does CRC occur in?

A

1) Age: older
>45 y/o
90% cases in persons >50 y/o
2) 75% of all cases occur in people with no known predisposing factors
3) Diet high in fruits, vegetables & fiber = decrease risk

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4
Q

What is the pathogenesis of CRC?

A

Sequential alterations in key growth regulatory genes

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5
Q

Describe the presentation of CRC

A

1) Unexplained or new onset Fe deficiency anemia
2) Emergency admission (obstruction, perforation, GI bleeding)
3) No symptoms in most early-stage CRC (diagnosed via screening)
4) Symptoms are due to growth of tumor into lumen or adjacent structures (advanced disease- ex/ obstruction, bleeding)

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6
Q

List the Sx of CRC (colorectal cancer)

A

1) Hematochezia, melena or + occult blood
2) +/- Abdominal pain
3) Unexplained iron deficiency anemia (IDA)
4) Change in bowel habits

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7
Q

CRC: What are some Sx of rectal cancer?

A

Tenesmus, rectal pain/bleeding, diminished caliber of stools

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8
Q

1) How common is metastatic CRC at time of Dx?
2) What are some Sx?

A

1) ~20% with distant metastasis at time of presentation (U.S.)
2) Regional lymph nodes, liver, lung, peritoneum (most common sites)
-Possible abd pain, early satiety, abdominal distention, supraclavicular adenopathy Virchow’s node (adv. mets) periumbilical nodule (Sister Mary Joseph’s nodule)

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9
Q

How is CRC diagnosed?

A

Histological evidence on biopsy from lower GI tract endoscopy or surgical specimen (majority adenocarcinomas)

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10
Q

Who should have a colonoscopy? What is the significance of colonoscopies relating to CRC?

A

1) Patients with suspected CRC (due to signs/symptoms) or candidate for screening (>= 45 yo) should have colonoscopy (or CT colonography)
2) Colonoscopy: most accurate & versatile diagnostic test
-CT colonography mostly used for incomplete colonoscopy

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11
Q

What are the labs for CRC? Are they needed?

A

Not recommended for screening/detection:
1) CBC: anemia (absence does not exclude CRC)
2) Tumor markers (CEA): not for screening (for prognosis)

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12
Q

What are some DDxs of CRC?

A

1) Broad (esp. among pts with abdominal pain & rectal bleeding)
2) Other malignancies (abdominal masses): Lymphomas, carcinoid, metastases from other primary cancers)
3) Benign lesions: Hemorrhoids, diverticulitis, infectious colitis, IBD

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13
Q

CRC: What are the stage groups derived from CT chest, abdomen & pelvis with IV/PO contrast? What is their significance?

A

1) I, II-IV: prognostic stage groups
-Correlates with the patient’s long-term survival (prognosis)
-Used to determine which patients should receive chemotherapy

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14
Q

Describe clinical staging of CRC

A

1) Once diagnosis made, local & distant extent determined for therapy & prognosis
2) CT chest, abdomen & pelvis with IV/PO contrast required for preoperative staging (MRI may be better for rectal cancers)
-I, II-IV: prognostic stage groups
-Correlates with the patient’s long-term survival (prognosis)
-Used to determine which patients should receive chemotherapy

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15
Q

Describe the TNM staging system for CRC

A

1) T: primary tumor
A tumor less than 2 cm is considered stage T1. Experts consider a tumor between 2 and 5 cm to be stage T2. If the tumor is greater than 5 cm, it’s typically stage T3. A tumor at stage T4 has spread into the chest/abd wall or skin.
2) N: status of the regional lymph nodes - N0: There is no cancer in nearby lymph nodes. N1, N2, N3: Refers to the number and location of lymph nodes that contain cancer.The higher the number after the N, the more lymph nodes that contain cancer.
3) M: distant metastasis - There are 2 M stages – M0 and M1. M0 meansthe cancer hasn’t spread to other parts of your body. M1 means the cancer has spread to other parts of the body.

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16
Q

CRC:
1) What is the Tx for colon cancer?
2) What is the Tx for rectal cancer?

A

1) Surgery & systemic chemotherapy
2) Surgery +/1 neoadjuvant & adjuvant therapy

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17
Q

What is one thing you need to do for mgmt of CRC? Why?

A

1) Regional dissection of lymph nodes
-At least 12 to determine staging
-Guides decisions about adjuvant therapy

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18
Q

CRC screening is endorsed by who?

A

1) USPSTF
2) Agency for Healthcare Policy & Research
3) American Cancer Society, &
4) every gastroenterology & colorectal surgery society

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19
Q

Why is screening for CRC so important?

A

1) Most cases of CRC arise from adenomatous or serrated polyps which progress to cancer
2) Polyp removal (polypectomy) prevents the majority of CRC

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20
Q

Describe CRC screening for avg risk pts (i.e. without personal or family history (1st degree relative) of colon polyps or CRC)

A

1) Majority of population
2) Men & women should be offered screening beginning at 45 y/o (age is strongest risk factor for CRC & adenomatous polyps)

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21
Q

Describe CRC screening for moderate (intermediate) risk

A

1) Personal history or family history of adenomatous polyps or CRC
2) Colonoscopy: preferred screening method 10 years prior to the age the relative was diagnosed and then q5 years if negative

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22
Q

Who is high risk for CRC? What is recommended for these pts?

A

1) Hereditary CRC syndrome, such as familial adenomatous polyposis (FAP) or Lynch syndrome (aka, hereditary nonpolyposis colorectal cancer-HNPCC)
2) Genetic counseling & special screening protocols are recommended

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23
Q

Describe CRC screening for:
1) Patients with h/o non-pre-cancerous polyps (ie, hyperplastic polyps)
2) Patients with h/o pre-cancerous polyps

A

1) Colonoscopy every 10 years (unless other risk factors for intermediate or high risk)
2) Colonoscopy every 3- 5 years

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24
Q

Patients with h/o pre-cancerous polyps with histologic features suggesting higher risk for progression to CRC usually require interval screening colonoscopy more frequently than _____________ years

A

5 years (~1-3 yrs)

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25
_____________ prevention through screening prevents deaths from CRC
Secondary
26
Describe primary and secondary prevention for CRC
1) Primary: Avoid or modify risk factors: smoking, physical inactivity, overweight or obesity, eating processed meat, excessive alcohol intake 2) Secondary: screening at appropriate time for determined risk
27
Describe the epidemiology of HCC
1) Most common primary malignant tumor of the liver 2) Men are generally more susceptible 3) Incidence increases progressively with advancing age in all populations
28
What are the 3 minor risk factors for HCC?
1) Smoking 2) Hereditary hemochromatosis 3) Alpha-1-antitrypsin deficiency
29
What are the Sx of HCC?
1) Weight loss - unintended 2) Weakness 3) Abdominal swelling - ascites 4) Nonspecific GI symptoms – nausea, malaise, jaundice
30
What are the 4 signs of HCC?
1) Hepatomegaly 2) Ascites 3) Jaundice 4) Wasting/cachexia
31
What are the clinical features of HCC? (including labs)
1) Anemia (normocytic) 2) Elevated alkaline phosphatase 3) HCV Ab, or HBV sAg /Ab 4) Elevated AFP level 5) Rare: malignant ascitic fluid cytology
32
What procedures should you do when examining HCC?
1) IV Contrasted CT, MRI or U/S 2) Arterial phase enhancement of the lesion followed by delayed hypointensity (“washout”) is most specific for hepatocellular carcinoma 3) Consider biopsy
33
How do you manage HCC?
1) Surgical resection 2) +/- Liver transplantation 3) Alcohol injection or radiofrequency ablation 4) Chemoembolization
34
Give examples of groups at high risk for HCC
1) h/o Chronic hepatitis B 2) Hepatitis B-induced cirrhosis 3) Hepatitis C-induced cirrhosis 4) Alcohol-induced cirrhosis
35
Give 3 examples of benign liver lesions
1) Cavernous hemangioma 2) Hepatocellular adenoma 3) Infantile hemangioendothelioma (benign vascular tumor of the liver usually 0-6 mo)
36
Describe the epidemiology of cavernous hemangioma
Most common benign liver tumor, congenital malformation that increases in size, more common in 3rd-5th decades of life, F>M
36
What are the clinical features of cavernous hemangioma?
Most small & asymptomatic; larger or multiple lesions cause upper abdominal pain, early satiety, nausea, vomiting; only physical feature hepatomegaly
37
Cavernous hemangioma: 1) How do you Dx? 2) How do you manage it?
1) U/S, MRI, or CT (do not biopsy) 2) Observation & surveillance imaging (asymptomatic), possible surgical resection (symptomatic)
38
Hepatocellular adenoma: What is the epidemiology?
Uncommon, benign, anabolic steroids, 25x risk with >9 years of OCP use
39
Hepatocellular adenoma: What are the clinical features?
Asymptomatic, acute hemoperitoneum; large, solitary, often superficial tumors may rupture (often while menstruating)
40
Hepatocellular adenoma: 1) How do you Dx? 2) How do you manage it?
1) U/S, MRI, needle Bx limited value, normal AFP 2) Surgery recommended, ligate hepatic artery, **discontinue OCPs**
41
Benign tumor-like liver lesions- Focal nodular hyperplasia (FNH): What should you do for large symptomatic lesions?
Should be resected
42
List some other nodular disorders (type of benign liver lesion)
1) Nodular regenerative hyperplasia: liver nodularity without fibrosis, associated with RA 2) Macroregenerative nodules occur in advanced cirrhosis or after massive hepatic necrosis
43
Benign liver lesions: List some types of hepatic cysts
1) Hydatid cysts (prior infection) 2) Fibrocystic disease of the liver 3) Solitary congenital cysts
44
Describe gastric cancer
1) Most pts symptomatic & have advanced, incurable disease at presentation 2) ~25% candidates for curative resection 3) Surgically curable early cancers usually asymptomatic (infrequent detection) 4) Screening only in high-incidence regions (Japan, Korea, Venezuela, Chile)
45
Gastric adenocarcinoma: Describe the epidemiology
4th most common cause of cancer death worldwide; higher rates in Japan, Asia, Eastern Europe, Chile, Colombia, & Central America; M>F; mean age 68; associated with environmental factors
46
Gastric adenocarcinoma: What are the features? (/Sx)
Usually asymptomatic until advanced; dyspepsia, vague epigastric pain, anorexia, early satiety, & weight loss, hematemesis or melena (ulcer,) postprandial vomiting (pyloric obstruction)
47
Gastric adenocarcinoma: 1) What are the features on exam? 2) What will labs show?
1) Gastric mass palpated (20%), + Guaiac-positive stools, Signs of metastasis on exam (Virchow node, Sister Mary Joseph nodule) 2) IDA, elevated ALP (if mets to liver)
48
Gastric adenocarcinoma: 1) How do you Dx? 2) How do you manage it?
1) Endoscopic biopsy 2) Surgical resection, perioperative chemotherapy or adjuvant chemoradiation, endoscopic mucosal resection for select patients, palliative surgery and/or chemotherapy for unresectable disease
49
Gastric lymphoma: 1) Etiology? 2) Features?
1) H. pylori infection risk factor, lymphocytic inflammatory response 2) Abdominal pain, weight loss, or bleeding; ulcer, mass or diffusely infiltrating lesion on endoscopy
50
Gastric lymphoma: 1) How do you Dx? 2) How do you manage?
1) Endoscopic biopsy 2) Depends on tumor histology, grade, & stage; radiation therapy, chemotherapy, and/or surgery; treatment for H. pylori in positive patients
51
Gastrointestinal stromal tumor (GIST): 1) What is the etiology? 2) What are the features?
1) Assumed origin from interstitial cells of Cajal- stem cells in wall of gut 2) Varies depending on primary tumor location (overt/occult GI bleeding (ulcer), obstruction, asymptomatic, abdominal pain, asymptomatic abdominal mass) -Can occur from esophagus to anus -Most common location is stomach & jejunum/ileum
52
Gastrointestinal stromal tumor (GIST): What are the features on PE?
Extragastrointestinal Stromal Tumors (EGISTs) in retroperitoneum, mesentery, and omentum; some asymptomatic; incidentally finding on imaging; often non-specific symptoms (bloating, early satiety)
53
Gastrointestinal stromal tumor (GIST): 1) How do you Dx? 2) How do you manage?
1) Histopathology, immunohistochemistry, & identification of disease-specific mutations 2) Depends on confidence in preoperative diagnosis, tumor location & size, extent of spread, & clinical presentation -Complete resection possible in most cases of localized GIST; high recurrence rate
54
Enteric neoplasms: 1) Give some examples of benign ones 2) Why is Dx difficult? 3) What is common regarding diagnosis?
1) Adenomas, leiomyomas, lipomas, hamartomas, & fibromas 2) Due to rare nature & non-specific &variable nature of signs & symptoms. 3) Delayed diagnosis common (frequently leads to discovery at late stage & poor outcomes)
55
(probs don't need to know) Describe the common locations of the following enteric neoplasms 1) Neuroendocrine tumor 2) Adenocarcinoma
1) Ilium 2) Duodenum
56
Enteric neoplasms: Sarcomas & lymphomas can develop throughout the entire ____________.
small bowel
57
Enteric neoplasms: Describe the epidemiology
1) >11,000 new cases & 1,700 deaths from small bowel cancer annually (U.S.) 2) Small bowel malignancies 3% of all GI tract neoplasms & approximately 0.6% of all cancers in U.S. 3) Mean age of diagnosis of small bowel neoplasm 65; M>F
58
Enteric neoplasms: Describe the features
1) Intermittent & crampy abdominal pain most common symptom 2) Other symptoms: weight loss, nausea with vomiting, GI bleeding 3) Intestinal obstruction more common than perforation
59
Neuroendocrine tumors (NET): 1) Describe the epidemiology 2) How do you manage it?
1) >90% pts with carcinoid syndrome have mets from SB primary NET; ~40% of primary SB malignancies; (highest incidence in 60s) 2) Depends on extent of disease; wide resection, palliative procedures
60
Neuroendocrine tumors (NET): Describe the features
SB NETs most commonly found in ileum; most asymptomatic; watery diarrhea & flushing m/c symptoms of carcinoid syndrome; pain m/c symptom in NET without carcinoid syndrome
61
Pancreatic cancer: Describe the epidemiology
Adenocarcinoma: most common neoplasm of pancreas (85%) 15% of all pancreatic cysts are neoplasms 75% in head, 25% in body & tail 2% of all cancers
62
Pancreatic cancer: Describe the prognosis
Surgical cure usually not possible: due to late presentation, only 15-20% of patients are candidates for pancreatectomy **>90% expected to die from the disease**
63
Pancreatic cancer: What are the risk factors?
Age, tobacco use, heavy alcohol use, obesity, chronic pancreatitis, DM, prior abdominal radiation, family history
64
True or false: Diarrhea is a feature of pancreatic cancer
True
65
List some more clinical features of pancreatic cancer
Advanced cases: hard periumbilical (Sister Mary Joseph’s) nodule Possibly mild anemia hyperglycemia, impaired glucose tolerance or diabetes elevated amylase or lipase
66
What may you find on imaging and testing for pancreatic cancer?
Possible evidence of obstructive jaundice CA19-9: 70% sensitive & 87% specific; not useful for early detection CT (multi-phase, thin-cut) detects mass in >80% MRI is good alternative U/S not useful due to interference from intestinal gas
67
Is EUS appropriate for pancreatic CA?
EUS – excellent for further imaging +/- bx, but not screening
68
Describe Dx and Tx of pancreatic cancer
1) Normal EUS excludes pancreatic cancer 2) ERCP: useful for ampullary or biliary neoplasm – can brush biopsy or place stent 3) MRCP: comparable to ERCP in diagnosing cancer, but not therapeutic 4) Radical pancreaticoduodenal (Whipple) resection is indicated for cancers strictly limited to the head of the pancreas, periampullary area, and duodenum (T1, N0, M0) 5) 5-years survival 20-25% (Whipple procedure) 6) Distal subtotal pancreatectomy: surgically resectable tumors of body or tail
69
Describe management of pancreatic CA
1) Endoscopic stenting to relieve jaundice in unresectable cases 2) Adjuvant chemotherapy is superior to no adjuvant therapy -Adjuvant chemoradiation also used in U.S. 3) Surgical duodenal bypass if obstruction expected; 4) Chemoradiation for palliation of unresectable cancer confined to pancreas 5) Pain control: celiac plexus nerve block
70