Pancreas Flashcards
Most common NET tumours of pancreas
1) Insulinoma
2) Gastrinoma
3) Non-functional
*Insulinoma has lowest malignant potential (10%), gastrinoma (60%), glucagonoma/VIPoma up to 80%
Imaging findings NET (US, CT, MR)
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
Causes of pancreatic lipomatosis
- CF
- Schwann-Diamond (kids, short stature)
- Cushings
- Chronic steroid
- Hyperlipidemia
What are the collections in AIEP? Necrotic pancreatitis?
AIEP:
<4 weeks, APFC
>4 weeks pseudocyst
Necrotizing pancreatitis:
<4 weeks, ANC
>4 weeks, WON
Most common anatomic variant of pancreas
Divisum (main pancreatic duct drains into minor Papilla)
Normally should drain inferiorly via Wirsung to major papilla
Most common imaging findings in chronic pancreatitis
Dilation and beading of panc duct, calcs, decreased T1 signal and enhancement and atrophy
Constellation of findings in IgG4 disease
Autoimmune pancreatitis Retroperitoneal fibrosis Fibrosing mediastinitis Sclerosing cholangitis Inflammatory pseudotumour Riedel's Thyroiditis Sialadenitis
Imaging features in serous versus mucinous cystadenoma
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
Which pancreatic lesion is seen in VHL?
Serous cystadenoma and NETs
Imaging findings SPEN tumour
Young patient, tail, solid/cystic (progressive enhancement), thick capsule T1/T2, hemorrhage**
Low grade malignancy* usually removed
Features concerning for malignancy in IPMN
*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
Management of incidental pancreatic cyst on CT
<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
Genetic syndromes with increased risk of panc adenoCa
Peutz-Jeghers, HNPCC, VHL
Genetic syndromes associated with pancreatic NETs
VHL, MEN1, NF1 (often multiple)
Gastrinoma most common in MEN1
Boundaries of gastrinoma triangle
2nd/3rd duodenum, cystic duct confluence, head of pancreas