Pancreas Flashcards

1
Q

Most common NET tumours of pancreas

A

1) Insulinoma
2) Gastrinoma
3) Non-functional

*Insulinoma has lowest malignant potential (10%), gastrinoma (60%), glucagonoma/VIPoma up to 80%

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2
Q

Imaging findings NET (US, CT, MR)

A

US: well circumscribed, hypoechoic mass
CT: early arterial enhancement, larger tumours can have necrosis, displace but don’t invade adjacent structures, can be cystic (esp if MEN1); include in ddx for cystic pancreatic lesion
MRI: T1 hypo, T2 bright, arterial enhancing

Increased uptake on Octreotide-111 (80% sensitivity) - not as sensitive for insulinomas

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3
Q

Causes of pancreatic lipomatosis

A
  • CF
  • Schwann-Diamond (kids, short stature)
  • Cushings
  • Chronic steroid
  • Hyperlipidemia
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4
Q

What are the collections in AIEP? Necrotic pancreatitis?

A

AIEP:
<4 weeks, APFC
>4 weeks pseudocyst

Necrotizing pancreatitis:
<4 weeks, ANC
>4 weeks, WON

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5
Q

Most common anatomic variant of pancreas

A

Divisum (main pancreatic duct drains into minor Papilla)

Normally should drain inferiorly via Wirsung to major papilla

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6
Q

Most common imaging findings in chronic pancreatitis

A

Dilation and beading of panc duct, calcs, decreased T1 signal and enhancement and atrophy

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7
Q

Constellation of findings in IgG4 disease

A
Autoimmune pancreatitis
Retroperitoneal fibrosis
Fibrosing mediastinitis
Sclerosing cholangitis
Inflammatory pseudotumour
Riedel's Thyroiditis 
Sialadenitis
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8
Q

Imaging features in serous versus mucinous cystadenoma

A

Serous - grandma, benign, panc head, microcystic (can appear solid), central scar +/- calcs
Mucinous - mother, panc body or tail, PRE-MALIGNANT,, unilocular (or a few large cystic spaces), peripheral calcs are highly specific

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9
Q

Which pancreatic lesion is seen in VHL?

A

Serous cystadenoma and NETs

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10
Q

Imaging findings SPEN tumour

A

Young patient, tail, solid/cystic (progressive enhancement), thick capsule T1/T2, hemorrhage**
Low grade malignancy* usually removed

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11
Q

Features concerning for malignancy in IPMN

A

*International consensus guidelines (2017)- Tanaka

High risk stigmata: main duct> 1 cm, enhancing nodule >5 mm, obstructive jaundice

Worrisome features: main duct 5-10 mm, cyst > 3 cm, enhancing nodule <5 mm, thickened enhancing wall, change in size > 5 mm in 2 years, lymphadenopathy, elevated CA 19-9

  • Main branch have up to 60% risk malignancy (Remove these); side branch only worry if >3 cm
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12
Q

Management of incidental pancreatic cyst on CT

A

<1.5 cm

  • age <65, re-image q1 years x 5 - then q2 x 2
  • age>65, re-image q2 years x 5 (stop if stable over 10 years)

*if grows >1.5cm, then proceed to EUS or FNA, OR if any other worrisome features or high risk stigmata

different guidelines for 1.5-2.5 cm, depending on presence of absence of connection to duct

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13
Q

Genetic syndromes with increased risk of panc adenoCa

A

Peutz-Jeghers, HNPCC, VHL

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14
Q

Genetic syndromes associated with pancreatic NETs

A

VHL, MEN1, NF1 (often multiple)

Gastrinoma most common in MEN1

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15
Q

Boundaries of gastrinoma triangle

A

2nd/3rd duodenum, cystic duct confluence, head of pancreas

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16
Q

Lipase hypersecretion syndrome

A

Acinar cell Ca

- Subcut fat necrosis, bone infarct, polyarthritis

17
Q

Branch duct IPMN associated with increased risk of:

A

synchronous adenocarcinoma

18
Q

Risk of malignancy with branch duct vs. main duct IPMN

A
Branch = 5%
Main = 35-50%