GI Malignancy Flashcards

1
Q

Risk factors for esophageal squamous cell cancer?

A

tobacco, alcohol, and caustic ingestion

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2
Q

when screening for esophageal cancer after lye ingestion?

A

20 years post ingestion

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3
Q

Populations that should have gastric cancer screening in the US?

A

strong family history of gastric cancer
FAP or Lynch syndrome,
extensive intestinal metaplasia

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4
Q

MALT lymphomas are characterized by presence of this genetic mutation?

A

the 11:18 chromosome translocation

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5
Q

celiac disease is associated with this tumor?

A

Enteropathy-associated T cell lymphoma

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6
Q

Tumor with positive synaptophysin and neuron-specific enolase

A

carcinoid tumor

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7
Q

PSC vs PBC in the risk of cholangiocarcinoma?

A

PSC increases risk; PBC does not

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8
Q

Patients who are co-exposed hepatitis B and THIS, have a dramatically higher risk of HCC than those with either risk factor individually. (produced by/)

A

Aflatoxin B1 (aspergillus)

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9
Q

exposure to this is associated with hepatic angiosarcoma?

A

vinyl chloride

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10
Q

African immigrants with hepatitis B virus should be screened starting at age?

A

20

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11
Q

Colonoscopy Surveillance After Colorectal Cancer Resection?

A

1 year -> 3 years -> every 5 years

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12
Q

congenital hypertrophy of the retinal pigment epithelium (CHRPE; ie “bear tracks”) found on eye exam.

next step? (why)

A

EGD/COLO (PPV of 90% for FAP)

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13
Q

Additional cancer surveillance in
1) FAP

A

1) Thyroid US; duodenoscope

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14
Q

Lynch Syndrome cancer screenings

A

colonoscopy every one to two years starting age 20 years,

After 30,
-EGD with antral biopsies q2-3 years
-pelvic exam with endometrial sampling and transvaginal ultrasound every year,
-urinalysis annually starting age 30 years.

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15
Q

Cowden - GI pathology?

A

-hamartomas and ganglioneuromas in the GI tract
-glycogenic acanthosis of the esophagus

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16
Q

Hereditary Diffuse Gastric Cancer - associated with this gene?

A

CDH1 (e-cadherin)

17
Q

Unfavorable histologic features of malignant polyps:

A

-poorly differentiated
-presence of angiolymphatic invasion
and/or
-positive margin of resection (<1-2 mm from the transected margin)

18
Q

Patient with freckles on her lips and colon polyps - diagnosis? Gene? polyp pathology?

Also needs to be screened for?

A

Peutz-Jeghers syndrome; STK11, hamartomas

Pancreatic cancer

19
Q

Management strategy for sessile serrated polyposis syndrome?

A

Colonoscopy every six to 12 months depending on polyp burden.

Colectomy for patients in whom endoscopic surveillance is not possible

20
Q

CDKN2A is the gene for?

A

familial atypical multiple melanoma and mole (FAMMM) syndrome

21
Q

paraneoplastic condition characterized by migratory superficial thrombophlebitis - aka? Associated with what malignancy?

A

Trousseau’s syndrome, suggestive of pancreatic adenocarcinoma

22
Q

Pathology of the polyp shows a saw-tooth appearance of the epithelium with basal crypt dilation and boot-shaped crypts without cytologic dysplasia. Type? Associated mutations?

A

sessile serrated polyp

BRAF mutations and CpG island methylation

23
Q

Tumor with spindle cells.

Metastatic or recurrent lesions are treated with?

A

GIST

imatinib

24
Q

Pancreatic cyst with columnar epithelium surrounded by ovarian-type stroma. Dx?

After surgical removal, postoperative surveillance?

A

mucinous cystic neoplasm

None. No role for imaging or EUS