Colorectal and pancreatic cancers Flashcards

(35 cards)

1
Q

what is a colectomy

A

resection/removal of any extent of the large bowel

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2
Q

what is a proctocolectomy

A

entire large intestine and rectum is removed

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3
Q

what is an “anastomosis”

A

remaining section of intestine are connected to complete the tube; may include ileostomy or colostomy, temporary or permanent

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4
Q

what is the concern with colonic polyps

A

malignant transformation; most colon cancers arise from previously benign adenomatous polyp

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5
Q

how are colonic polyps diagnosed

A

colonoscopy

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6
Q

what are familial adenomatous polyposis

A

multiple polyps

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7
Q

what are the clinical presentations of colonic polyps

A

most asymptomatic
rectal bleeding usually occult and rarely massive, is most frequent complain
cramps, abdominal pain, or obstruction may occur with large polyps

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8
Q

what is the treatment of colonic polyps

A

complete removal during colonoscopy
follow up surgical resection
and follow up surveillance colonoscopy

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9
Q

what are preventative measures for colonic polyps

A

ASA and Cox-2 inhibitors may help prevent formation of new polyps in patients with polyps or colon cancer

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10
Q

What is FAP

A

Familial adematous polyposis
hereditary disorder (autosomal dominant) causing Numerous colonic polyps and frequently resulting in colorectal cancer, often by age 40

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11
Q

what are the subtypes of FAP

A

classic FAP
Attenuated FAP (AFAP_
Gardner syndrome
Turcot Syndrome

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12
Q

what are clinical presentations of FAP

A

most are asymptomatic
if symptomatic usu present wtih rectal bleeding, usually occult
other associated findings: Osteomas, usu of jaw, extra missing, unerupted teeth, etc

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13
Q

what is the treatment of FAP

A

yearly colonoscopy once polyps are found until a colectomy is scheduled
colectomy done as soon as possible after diagnosis made

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14
Q

what is hematochezia

A

blood in stool

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15
Q

what is the most common colorectal cancer

A

adenocarcinomas

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16
Q

what are predisposing factors for colorectal cancers

A

FAP
ulcerative colitis and Crohn’s
Diets in low fiber, high animal protein, fat and refined carbs
cacinogens in diet

17
Q

what are risk factors for CRC

A

smoking, ETOH intake, increased body weight
T2DM
red/processed meats

18
Q

when does CRC screenings start

A

average-risk patients: start at 45yo and continue until 75
every 10 years or annually FIT as preferred screening test

19
Q

what are the screening tests for CRC

A

colonoscopy: every 10 years
Fecal occult blood test (FOBT): every year
flexible sigmoidoscopy: every 5 years
CT colonography; every 5 years
Fecal immunochemical test (FIT)
Fecal DNA testing

20
Q

what is the treatment of CRC

A

surgery
neo/adjuvant therapy: chemo and radiation
Palliation

21
Q

what is CEA level

A

serum carcinoembryonic antigen
elevated in 70% in pts with CRC
-good for surveillance

22
Q

what are the types of pancreatic CA

A

adenocarcinoma
neuroendocrine
cystadenocarcinomas
intraductal papillary-mucinous tumor

23
Q

where do most exocrine tumors develop from

A

ductal and acinar cells: usually adenocarcinomas

24
Q

what are prominent risk factors for adenocarcinomas

A

smoking
hx chronic pancreatitis
obesity
male
african american

25
what is the clinical presentation of pancreatic CA
Early sx are non-specific: pain and weight loss cancer can cause diabetes: glucose intolerance exocrine insufficiency malabsorption
26
what are the preferred tests for pancreatic CA
abdominal CT or MRI followed up endoscopic ultrasound with FNA (EUS/FNA)
27
what type of pancreatic cancers present with jaundice
head of the pancreas CA
28
what are the lab tests run with Dx/workup of pancreatic CA
CBC, CMP: elevation of alk phos and bilirubin, amylase/lipase usual normal CA 19-9
29
what is a pnacreaticoduodenectomy
Whipple procedure
30
what is the treatment of pancreatic CA
whipple +/- chemo/radiation symptom control/palliative care
31
what is neuroendocrine pancreatic CA
arise from islets and gastrin-producing cells and often produce many hormones may appear in other organs, particularly duodenum, jejunum andlung
32
what are the manifestations of neuroendocorine pancreatic CA
functioning: hyper-secrete specific hormone, causing various syndrome non-functioning: may cause obstructive symptoms of biliary tract or duodenum, bleeding into Gi tract or abdominal masses
33
what is the tx of neuroendocrine pancreatic cancer
surgical resection if mets preclude curative surgery, various anti-hormone tx may be tried
34
what is cystadenocarcinoma
RARE adenomatous pancreatic cancer that arises as malignant degeneration of a mucinous cystadenoma manifests as upper abdominal pain, palpable abd mass
35
what is intraductal papillary-mucinous tumor
results in mucus hypersecretion and ductal obstruction symtpoms: pain and recurrent pancreatitis dx: CT/MRI