Dr. Starling Flashcards

1
Q

Barrett’s esophagus

A
  • intestinal metaplasia: strat squamous epith. -> non-ciliated cuboidal epith. with goblet cells
  • red, velvet patches
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2
Q

risk factors for esophageal SCC

A
  • EtOH and Tobacco

- middle 1/3

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3
Q

risk factors for esophageal adenocarcinoma

A
  • obesity and GERD
  • due to Barrett’s
  • distal 1/3
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4
Q

progressive difficulty swallowing solids then liquids + unexplained weight loss

A

esophageal adenocarcinoma

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5
Q

chronic gastritis

A
  • due to H. pylori -> increase risk of MALTlymphoma
  • due to autoimmune -> risk of NE tumor

-both increased risk for gastric adenocarcinoma

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6
Q

FAP

A

-associated w/ fundic gland polyps -> can lead to dysplasia and gastric adenocarcinoma

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7
Q

sites of gastric adenocarcinoma metastases

A
  1. left supraclavicular node (virchow node)
  2. periumbilical (sister Mary Joseph nodule)
  3. left axillary node (irish node)
  4. ovary (Krukenburge tumor)
  5. pouch of Douglas (blummer shelf)
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8
Q

intestinal gastric adenocarcinoma

A

-ulcerated with heaped up margins

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9
Q

diffuse gastric adenocarcinoma

A
  • no heaped up margins
  • thickened rugae -> linitis plastica
  • signet ring cells
  • loss of E-cadherin mut.
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10
Q

prognosis and treatment of gastric adenocarincoma

A
  • depth of invasion and extent of nodal/distant metastasis best predictors
  • surgery preferred
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11
Q

Gastric Lymphoma - Extranodal marginal zone B cell lymphoma (aka MALToma)

A
  • due to H. pylori

- t (11;18) (q21;q21)***

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12
Q

GIST

A
  • most common mesenchymal tumor
  • arise from interstitial cells of Cajal (pacemakers)
  • Carney triad, Neurofibromatosis type 1, Carney Stratakis syndrome
  • histo: paranuclear vacuoles with KIT marker
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13
Q

carcinoid tumor

A
  • neuroendocrine tumor of GI tract -> more aggressive if arise in small intestine
  • can arise in lungs
  • markers: synaptophysin and Chromagranin A+
  • MIDGUT tumors most aggressive
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14
Q

hemartomatous polyps

A
  • associated w/ Juvenile Polyps -> SMAD4 mut.

- associated w/ Peutz-Jegher syndrome -> HYPERPIGMENTATION and STK11 mut.

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15
Q

adenomatous polyps

A
  • risk of colorectal carcinoma
  • start colonoscopy at age 50
  • start 10 years prior to when family member was diagnosed
  • villous type has highest risk of cancer
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16
Q

sessile serrated adenomatous polyps

A
  • full length of gland and precursor to colorectal carcinoma
  • hyperplastic serrations don’t run full length of gland
17
Q

adenoma-carcinoma sequence path

A

-mutations in APC/B-catenin

-

18
Q

microsatellite instability path

A
  • DNA mismatch repair enzyme mut.

- mut. in MSH2, MSH6, MLH1, PMS2 -> CIMP and BRAF

19
Q

Fe deficiency anemia in old man or post-menopausal women

A

GI cancer until proven otherwise

-need colonoscopy

20
Q

what is the most common place for colorectal adenocarcinoma metastasis?

A

LIVER

21
Q

FAP

A
  • APC mutation
  • 100% progress to CRC; >100 polyps
  • adenoma-carcinoma sequence -> LEFT side
    1. Garner’s syndrome -> FAP + osteoma, skin, retinal involvement
    2. Turcot syndrome -> FAP + brain (gliomas and medulloblastomas)
22
Q

HNPCC -Lynch syndrome

A
  • mismatch repair genes (MMR) mutation
  • MLH1, MSH2 mut.
  • microsatellite path -> RIGHT side
  • most common form of syndromic colorectal carcinoma
23
Q

what anal canal tumor is associated w/ HPV and condyloma acuminatum?

A

squamous cell carcinoma

-strat. squamous epith.

24
Q

mutation most commonly associated w/ tubular adenomas?

A

KRAS

-BRAF seen in villous sessile adenomas