Ch. 14 - Pancreas & Biliary Tree Flashcards

1
Q

What are the indications for pancreatobiliary FNA?

A

Unexplained pancreatic mass, bile stricture

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2
Q

How are pancreatic head masses sampled? Pancreatic body/tail?

A

Head masses are sampled through duodenum, body & tail through the stomach.

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3
Q

What complications are associated with pancreatic FNA?

A

Acute pancreatitis, perforation, cholangitis

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4
Q

What chemical testing can be performed on pancreatic cyst fluid?

A

CEA, amylase, KRAS/GNAS mutations.

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5
Q

What are the three normal components of pancreatic parenchyma?

A

Acinar cells, ductal cells, and islet cells (rare).

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6
Q

Describe the cytology of normal pancreatic acini.

A

Grapelike aggregates with eccentric nuclei, fine granular chromatin, and indistinct cell borders.

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7
Q

Describe the cytology of pancreatic ductal epithelium.

A

Flat cohesive sheets with even nuclear spacing (honeycombing). Should not have visible cytoplasmic mucin!

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8
Q

In what context may pancreatitis be sampled by FNA?

A

Only in chronic pancreatitis which may have mass-forming fibrosis. This is most prominent in autoimmune pancreatitis.

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9
Q

Describe the cytology of pancreatic ductal adenocarcinoma (PDAC)

A

High cellularity, irregular clusters with uneven distribution of cells (“drunken honeycomb”), marked atypia and anisonucleosis (>4:1).

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10
Q

Recall some variants of PDAC.

A

Adenosquamous, undifferentiated (with or without osteoclast-like giant cells), colloid, hepatoid, medullary, signet ring

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11
Q

Why is pancreatic intraepithelial neoplasia (PanIN) never sampled by FNA?

A

It is an in situ lesion and does not present with a mass.

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12
Q

Describe the cytology of pancreatic neuroendocrine tumor (PanNET).

A

Highly cellular with some pseudorosetting, eccentric nuclei with salt and pepper chromatin and rare endocrine atypia.

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13
Q

How are PanNETs graded?

A

By proliferation rate (1 / 2-20 / >20) and by Ki67 (<3% / 3-20% / >20%).

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14
Q

What may be functionally secreted by PanNETs, and why is that clinically significant?

A

Insulin, glucagon, somatostatin, VIP, serotonin, even ACTH and calcitonin. They manifest with clinical symptoms and are often detected earlier.

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15
Q

What are some specific markers for PanNET?

A

Besides the usual neuroendocrine markers, PanNETs stain for Islet-1 and PAX-8.

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16
Q

Describe the cytology of acinar cell carcinoma.

A

Solid-cellular pattern of monomorphic cells with granular cytoplasm (and background granules), smooth nuclei and prominent nucleolus.

17
Q

Describe the cytology of solid pseudopapillary neoplasm.

A

Cellular aspirate with myxoid/hyalinized vascular stalks. Loose cells have finely vacuolated cytoplasm, grooved nuclei, and inconspicuous nucleoli. Background shows foam cells & debris (cystic degeneration).

18
Q

What are some useful IHC markers for acinar cell carcinoma?

For SPN?

Which has a worse prognosis?

A

ACC: Trypsin (best), lipase, chymotrypsin, and phospholipase A2

SPN: Alpha1-antitrypsin, PR, CD56, CD10, CD117, and nuclear+cytoplasmic beta-catenin.

ACC has a worse prognosis.

19
Q

Describe the cytology of pancreatoblastoma.

A

An epithelial component composed of syncytial groups and isolated cells with distinctive “squamoid corpuscles?, and a stromal component composed of primitive spindle cells.

20
Q

Recall some different type of pancreatic cysts.

A

Pseudocyst, serous cystadenoma, lymphoepithelial cyst, mucinous cystic neoplasm, intraductal papillary mucinous neoplasm.

21
Q

Describe the cytology of pseudocyst.

A

Thin nonmucinous fluid with inflammatory cells and hematoidin.

22
Q

Describe the cytology of serous cystadenoma.

A

Low cellularity, clean background, maybe some siderophages and small clusters of glycogenated cells. Hard to diagnose on cytology…

23
Q

Describe the cytology of lymphoepithelial cyst.

A

Anucleate squames (keratinaceous debris), squamous cells and lymphocytes. May have some cholesterol clefts; overall resembles an EIC.

24
Q

In general, what cyst chemistry profile is expected from benign pancreatic cysts?

A

High amylase, low CEA, no KRAS or GNAS mutations.

25
Q

Describe the cytology of MCN & IPMN.

A

Hypocellular, with variable amounts of mucin and variable dysplasia in the epithelial component.

Note: They cannot be distinguished from one another on cytology.

26
Q

Distinguish the clinical features of MCN and IPMN.

A

MCN: Exclusively affects women, usually in the pancreatic tail. Does not communicate with ductal system.

IPMN: Affects both sexes, involves main duct, branch duct, or both.

27
Q

Describe the cytology of ectopic splenic tissue in pancreas.

A

Highly vascular, with many lymphocytes. Distinguishing feature is CD8+ vessels on cell block.

28
Q

How can KRAS/GNAS mutational analysis distinguish MCN and IPMN?

A

KRAS point mutations are seen in both MCN and IPMN. GNAS abnormalities are only seen in IPMN.

29
Q

What are some useful stains to identify PDAC?

A

SMAD4 (DPC4), p53.

30
Q

Distinguish between the clinical features of serous cystadenoma and lymphoepithelial cyst.

A

Serous cystadenoma: Affects women, usually in tail of pancreas. Can be microcystic, oligocystic…

Lymphoepithelial cyst: Affects mostly middle-aged men. Can be multifocal.