Upper GI Pathology Flashcards

1
Q

Barrett Esophagus

A

Premalignant condition resulting from chronic injury

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2
Q

Metaplasia of lower esophageal mucosa from —– to ——

A

Stratified squamous epithelium to nonciliated columnar epithelium w/ GOBLET CELLS

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3
Q

Non-goblet columnar epithelial

A

Similar to stomach surface

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4
Q

Goblet cells

A

acid mucin vacuole distends cytoplasm & compress nucleus

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5
Q

Absorptive cells

A

Paneth cells
Endocrine cells

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6
Q

Classification

A

Barrett esophagus does not have metastatic potential by itself

Negative dysplasia vs Positive dysplasia (low-grade, high-grade)

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7
Q

Positive dysplasia low grade

A

Barrett’s mucosa

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8
Q

Positive dysplasia high grade

A

Higher chance of progressing to invasive esophageal adenocarcinoma

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9
Q

Cause of barrett esophagus

A

GERD

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10
Q

Risk factors for Barrett Esophagus

A

Male, 5th decade, whites
Obesity
Smoking
Alcohol
Hiatal hernia

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11
Q

Micro of Barrett Esophagus

A

Columnar metaplasia w/ goblet cells involving esophagus

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12
Q

Endoscopy

A

Biopsy required for diagnosis
Velvety mucosa
Salmon-colored tongue above esophageal junction (extend into distal esophagus GE junction)

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13
Q

Biomakers that predict prognosis risk for Barrett Esophagus

A

Abnormalities of p16 (INK4/CDKNA)

Frequent TP53 mutations

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14
Q

Esophageal adenocarcinoma

A

Malignant epithelial tumor of the esophagus w/ glandular differentiation

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15
Q

Incidence of Esophageal adenocarcinoma

A

Increasing 2/2 increasing obesity, GERD, declining H. pylori infection

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16
Q

Demographic of adenocarcinoma

A

67 yo male

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17
Q

Etiology of adenocarcinoma

A

All develops in the setting of intestinal metaplasia (Barrett’s esophagus)

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18
Q

Risk fx for adenocarcinoma

A

Obesity
Smoking (sq cell carcinoma of esophagus)
Alcohol
Genetic predisposition

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19
Q

Location of adenocarcinoma

A

Distal 1/3 esophagus

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20
Q

Early gross path of adenocarcinoma

A

Ulcer
Nodule
Polyp
Plaque

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21
Q

Late gross path of adenocarcinoma

A

Fungating or annular
Ulcer

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22
Q

Micro of adenocarcinoma

A

Gland crowding
Cribriform plates
Dirty necrosis

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23
Q

Adenocarcinoma advanced tumors sx

A

Progressive dysphagia (solids –>liquids)
WT loss
Retrosternal/epigastric pain

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24
Q

Squamous cell carcinoma of the esophagus

A

Malignant epithelial neoplasm w/ squamous cell differentiation

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25
Keratinocyte-like cells that may contain intercellular bridges and/or keratinization
Pathology of squamous cell carcinoma of the esophagus
26
Risk fx of squamous cell carcinoma of the esophagus (1/2)
Tobacco: majority, potentiates risk assoc w/ alcohol Alcohol Japanese alcoholics -- ALDH2 gene
27
ALDH2 gene (aldehyde dehydrogenase 2 gene)
Japanese alcoholics at risk for squamous cell carcinoma of the esophagus
28
Risk fx of squamous cell carcinoma of the esophagus (2/2)
Nitrosamines in pickled/moldy foods; vitamin deficiencies Plummer-vinson syndrome Achalasia Tylosis (AD skin disorder) Celiac disease (risk d/t iron deficiency anemia) Prior corrosive ingestion
29
Gastric adenocarcinoma
Malignant epithelial cell tumor of gastric origin
30
Early Gastric Adenocarcinoma
Limited to mucosa & submucosa
31
Advanced Gastric Adenocarcinoma
Invade muscularis propria or more deeply
32
pathogenesis gastric Adenocarcinoma
Multifactorial disease w/ strong environmental influences Chronic mucosal injury
33
Risk factors gastric adenocarcinoma
1. H. pylori infection (CagA) 2. GERD 3. Bile reflux gastropathy following gastric surgery 4. Autoimmune gastritis 5. Diet (dried salted/smoked meats) 6. Smoking
34
Gross/Micro pathology of gastric adenocarcinoma
1. Gland-forming tumors -- intestinal-type carcinoma form bulky tumors 2. Diffuse-type carcinoma -- diffuse infiltrative growth pattern (signet ring cell carcinoma)
35
Infiltrating glands w/ fused, papillary, or cribriform architecture Cells contain LARGE, hyperchromatic nuclei
Gland-forming tumors --> intestinal-type carcinoma
36
Signet ring cell carcinoma Large mucin vacuole compresses the nucleus Cells grow in nests, cords, singly Round, irregular nuclei & variable amounts of eosinophilic cytoplasm
Diffuse-type gastric adenoma carcinoma --> diffuse infiltrative growth pattern
37
Plastica
not pliable w/ an appearance similar to "leather bottle" stomach CDH1 mutation gastric adenocarcinomas (E-cadherin)
38
Early Gastric Adenocarcinoma clinical features
Asymptomatic Ab pain Mimics peptic ulcer disease: epigastric pain, dyspepsia (sister mary joseph nodule)
39
Advanced Gastric Adenocarcinoma clinical features
Ab pain (epigastrium) Anemia Vomiting WT Loss
40
Met/paraneoplastic signs: Gastric Adenocarcinoma clinical features
Intra Abdominal dissemination & ascites Ovaries (Krukenberg tumor) Aconthosis nigricans/Leser-Trelat sign Lymphatic spread --> L supraclavicular node (Virchow node) Hematogenous spread --> liver & lung St. Mary J Nodule
41
Gastric marginal zone (MALT) lymphoma
Low-grade lymphoma composed of heterogenous B-cell population
42
Gastric marginal zone (MALT) lymphoma
Stomach is common site of extranodal lymphomas
43
Cause of Gastric marginal zone (MALT) lymphoma
Most assoc w/ chronic H. pylori infection CagA+ most immunogenic
44
Trisomies 3, 12, 18
Common in Cause of Gastric marginal zone (MALT) lymphoma
45
Translocation associated with Gastric MALT lymphoma
t(11;18)(q21;q21)
46
Diffuse proliferation of small-medium sized lymphocytes → monocytoid appearance w/ abundant pale cytoplasm
Microscopic signs of Gastric MALT
47
Gastric glands infiltrated by lymphocytes (lymphoepithelial lesions) & uniform monocytoid morphology of the cells infiltrating the lamina propria
Microscopic signs of Gastric MALT
48
GI stromal tumor
Mesenchymal tumor of the GI tract w/ characteristic histologic, immunohistochemical, molecular features
49
GI stromal tumor molecular sign
CD117, KIT Neurofibromatosis type I
50
Amenable to tyrosine kinase inhibitor therapy (imatinib)
GI Stromal Tumor -- KIT mutations = 85% of cases
51
GI Stromal Tumor -- AD familial syndrome
Mutations in exons 11 & 13 of KIT
52
Carney triad
GI Stromal Tumor Pulm chondroma Catecholamine-secreting paraganglioma
53
GI Stromal Tumor: Older Adults
KIT & PDGFRA-mutated GISTs (60-65yo)
54
GI Stromal Tumor: <21 yo
GISTs are SDH deficiency
55
Well-defined round-oval tumor w/ epicenter in muscularis propria
Gross features of GI Stromal Tumor
56
Firm to fleshy or gelatinous cut surface
Gross features of GI Stromal Tumor
57
Hemorrhage & cystic degeneration in large tumors
Gross features of GI Stromal Tumor
58
Site of GI Stromal Tumor
Stomach>> Jejunum/ileum>> duodenum>rectum
59
Micro of GI Stromal Tumor
neoplastic cells → spindled/epithelioid mesenchymal neoplasm thought to arise/differentiate toward interstitial cells of Caja (ICC) or pacemaker cells
60
GI bleeding d/t mucosal ulceration (MOST COMMON) GI obstruction, abdominal pain Incidental findings during surgery
Clinical features of GI Stromal Tumor