Carcinoid Syndrome Flashcards

1
Q

what is the def of CS

A

a group of associated symptoms caused by release of humoral factors (biogenic amines, polypeptides, prostaglandins) from carcinoid tumours

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2
Q

what are carcinoid tumours

A

slow growing neuroendocrine tumours

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3
Q

what is the aetiology of CS

A

carcinoid tumours are slow growing neuroendocrine tumours mostly derived from serotonin-producing enterochromaffin cells
produce secretory products such as serotonin, histamine, prostaglandins
can be classified into fore-, mid- or hindgut tumours
75-80% of CS patients have small bowel carcinoids
common sites for carcinoids tumours are include appendix & rectum where they are benign & non-secretory
hormones released into portal circulation are metabolised by liver therefore symptoms do not appear until there are hepatic metastases (resulting in secretion of tumour products into the hepatic veins).

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4
Q

what is the epi of CS

A

rare
asymptomatic carcinoid tumours are more common
10% of multiple endocrine neoplasia (MEN) type 1 patients have carcinoid tumours

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5
Q

what history is associated with CS

A
paroxysmal flushing
diarrhoea
crampy abdominal pain
wheeze
sweating
palpitations
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6
Q

what examinations findings are associated with CS

A

facial flushing, telangiectasia (broken capillaries), wheeze
RS heart murmurs
-tricuspid stenosis, regurgitation or pulmonary stenosis
nodular hepatomegaly in cases of metastatic disease

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7
Q

what examination findings are associated with carcinoid crisis

A

profound flushing
bronchospasm
tachycardia
fluctuating BP

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8
Q

what investigations would be performed in suspected CS

A

24h urine collection
-5-HIAA levels (a metabolite of serotonin)
bloods
-plasma chromogranin A & B, fasting gut hormones
radioisotope scan
-radiolabelled somatostatin analogue to localise tumour

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9
Q

what are the causes of high 5-HIAA (false positives)

A

bananas & avocados
caffeine
paracetamol

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