Colorectal and pancreatic cancers Flashcards

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
Q

what is the clinical presentation of pancreatic CA

A

Early sx are non-specific: pain and weight loss
cancer can cause diabetes: glucose intolerance
exocrine insufficiency
malabsorption

26
Q

what are the preferred tests for pancreatic CA

A

abdominal CT or MRI
followed up endoscopic ultrasound with FNA (EUS/FNA)

27
Q

what type of pancreatic cancers present with jaundice

A

head of the pancreas CA

28
Q

what are the lab tests run with Dx/workup of pancreatic CA

A

CBC, CMP: elevation of alk phos and bilirubin, amylase/lipase usual normal
CA 19-9

29
Q

what is a pnacreaticoduodenectomy

A

Whipple procedure

30
Q

what is the treatment of pancreatic CA

A

whipple +/- chemo/radiation
symptom control/palliative care

31
Q

what is neuroendocrine pancreatic CA

A

arise from islets and gastrin-producing cells and often produce many hormones
may appear in other organs, particularly duodenum, jejunum andlung

32
Q

what are the manifestations of neuroendocorine pancreatic CA

A

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
Q

what is the tx of neuroendocrine pancreatic cancer

A

surgical resection
if mets preclude curative surgery, various anti-hormone tx may be tried

34
Q

what is cystadenocarcinoma

A

RARE adenomatous pancreatic cancer that arises as malignant degeneration of a mucinous cystadenoma
manifests as upper abdominal pain, palpable abd mass

35
Q

what is intraductal papillary-mucinous tumor

A

results in mucus hypersecretion and ductal obstruction
symtpoms: pain and recurrent pancreatitis
dx: CT/MRI