Pancreatic cancer Flashcards

1
Q

what’s the most common form of cancer in the pancreas? where does it usually occur?

A

ductal carcinoma at the head of the pancreas

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2
Q

what is the prognosis for ductal carcinoma of the pancreas and why?

A

very poor prognosis as it usually presents quite late and rarely early enough for curative treatment.
metastasizes early to lymph nodes, peritoneum, and liver (portal drainage)

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3
Q

what are the risk factors for developing pancreatic carcinomas?

A
  • smoking
  • chronic pancreatitis
  • recent onset of diabetes
  • FHx
  • late-onset of diabetes (above 50)
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4
Q

what are the clinical features of ductal pancreatic carcinomas of the head and why do they develop?

A
  • obstructive jaundice: compression of the bile duct)
  • -> typically painless early on and leads to steatorrhea and dark urine
  • Abdo pain (deep gnawing epigastric) : invasion of the coeliac plexus / secondary to pancreatitis
  • weight loss- cancer/ exocrine dysfunction

less common:

  • steatorrhea
  • pancreatitis
  • diabetes Mellitus
  • thrombophlebitis migrans –> repeated thrombosis of superficial veins – hypercoagulable state
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5
Q

what is Courvoisier’s law??

A

In the presence of jaundice and an enlarged/palpable gallbladder, the gall bladder is unlikely to be the cause, therefore, malignancy of the biliary tree/pancreas should be considered

  • gall stones –> chronic inflammation –> fibrosis and hypertrophy of the gall- bladder wall –> unlikely to distend.
    in cancers the obstruction develops quickly, therefore, the gall bladder wall can distend
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6
Q

what are some of the differential diagnoses for pancreatic ca??

A

obstructive jaundice: gall stone obstruction, cholangiocarcinoma, benign gall bladder stricture

epigastric Abdo pain - peptic ulcer, gall stone disease, MI, GORD, oesophagitis, pancreatitis, AAA

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7
Q

what investigations are performed in suspected pancreatic cancer?
what are the findings

A

lab tests
- FBC: anaemia / thrombocytopenia
- LFTs: raised bilirubin, ALP and GGT –> obstructive
(CA19-9 used more for tracking treatment rather than initial diagnosis)

imaging
USS - pancreatic mass/dilation of the biliary tree (liver metastases in late-stage)
a pancreatic protocol CT scan - tumour extent/ liver metastases/ vascular invasion in SMA/ coeliac axis
PET CT - looks for metastases
EUS - fine-needle aspiration to evaluate lesion for treatment or diagnosis. can also show added detail to determine if the lesion is resectable
MRCP/ERCP - diagnosis of gall stone/ biliary tree pathology

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8
Q

what is the surgical management for ductal pancreatic ca??

A

cancers in the head of the pancreas:

  • Whipple’s procedure (pancreaticoduodenectomy):
    1) involves removal of the antrum of the stomach, the head of the pancreas, 1st and 2nd part of duodenum, common bile duct and the gallbladder. –> all have common arterial supply - gastroduodenal artery
    2) tail of pancreas and hepatic duct attached to the jejunum (allow juices to flow into bowel) and stomach anastomosed with the jejunum
  • check teach me surgery diagram
  • adjuvant chemotherapy (5-fluorouracil) after surgery
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9
Q

Outline the palliative care of ductal pancreatic adenocarcinma.

A

this is done for the majority of patients

surgical:
- a biliary stent may be put in via ERCP to relieve jaundice and itching
- triple bypass operation

chemotherapy may be initiated

exocrine insufficiency (especially post Whipple’s): Creon

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10
Q

what is the prognosis for ductal adenocarcinoma?

A

5- year survival is less than 5%

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11
Q

describe teh difference between sunction and non-function endocrine tumours?

A

functional: actively secrete hormone –> signs and symptoms associated with this
non-functionl: dont secret hormones –> signs and symptoms due to maliganat spread

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12
Q

what is an endocrine cancer of the B cells and how does it present?

A

insulinoma

symptomatic hypogltcaemia : seating, changing mental state -improving with consumption of carbs

*investigations: hyperinsulanemaia –> CT
usually benign

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13
Q

what cells are affected in glucagonomas?

what are the clinical features?

A

affects alpha cells

hyperglycaemia –> diabetes mellitis and migratory necrolytic erythema (skin condition - check images)

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14
Q

what is zollinger-ellison syndrome?

how does it present ?

A

cancer of the G cells –> gastrinoma

severe peptic ulcers
diarrhoea

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15
Q

what cells are affected in somatastatinomas?

what are thee clinical features?

A

delta cells

diabetes mellitus
steatorrhea, gallstones –> inchibition of CCK
weight loss and reduced HCL –> inhibition of gastrin

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16
Q

what are the Multiple Endocrine Neoplasia syndromes?

A

these are autosomal dominant inherited syndroms.
thesere 3 forms :

MEN1 : islet cell tumours, pituatary adenoma and Parathyroid hyperplasia
MEN2a: medullary thyroid ca (esp in childhood), phaechromocytoma and parathyroid hyperplasia/ adenoma
MEN2b: medullary thyroid ca, phaechromocytoma and mucosal/GI neurofibromas and marfanoid habitus(syndrome of marfan’s symptoms)

17
Q

what are the general principle of investigation and managemnt in endocrine pancreatic ca?

A

investigations: CT, MRI +/- EUS
management :
small non-functional = observed
larger/functioning: resected

18
Q

which type of cystic neoplasm is most likely to become malignant and which is less likely?

A

mucinous cyst = more likely to become malignant

serous cyst = less likely to become malignant

19
Q

what are the investigations performed for a potential cystic neoplasm?

A

typically CT and EUS allow aspiration for cytology. these help to differentiate between pseudocysts, serous and mucinous adenocarcinoma,s and cystadenocarcinoma

20
Q

what are the treatments for different cysts?

A

mucinous cyst –> resection
serous cyst –> observation
and cancerous cysts –> resection