Hepatobiliary Surgery Flashcards

(62 cards)

1
Q

Gallstones

A

90% remain ASx
slightly more in F
western ^

Aetiology
 Lithogenic bile: Admirand’s Triangle
 Biliary sepsis
 GB hypomotility → stasis
 Pregnancy, OCP
 TPN, fasting

Composition
 Phospholipids: lecithin
 Bile pigments (broken down Hb)
 Cholesterol

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2
Q

Gall stones (cholesterol stones)

A

20%
 Large
 Often solitary

Formation ↑ according to Admirand’s Trangle
 ↓ bile salts
 ↓ lecithin
 ↑ cholesterol

Risk factors
 Female
 OCP, pregnancy
 ↑ age
 High fat diet and obesity
 Racial: e.g. American Indian tribes
 Loss of terminal ileum (↓ bile salts)
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3
Q

Gall Stones (Pigment and mixed)

A

Pigment Stones: 5%
 Small, black, gritty, fragile
 Calcium bilirubinate
 Associated c¯ haemolysis

Mixed Stones: 75%
 Often multiple
 Cholesterol is the major component

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4
Q

Gallstones Complications

A

Gallbladder

  • Biliary colic
  • Acute Cholescystitis w/(o) empyema
  • chronic cholecystisis
  • Mucocoele
  • Carcinoma
  • Mirizzi’s syndrome

CBD - common biliary duct

  • obstructive jaundice
  • pancreatitis
  • cholangitis

Gut - galstone ileus

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5
Q

Biliary Colic

description + presentation

A

Gallbladder Spasm against stone impacted in neck of gallbladder - Hartmann’s Pouch
Less commonly stone in CBD

Presents
Biliary colic
 RUQ pain radiating → back (scapular region)
 Assoc. c¯ sweating, pallor, n/v
 Attacks may be ppted. by fatty food and last <6h

o/e may be tenderness in right hypochondrium
± jaundice if stones passes in to CBD

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6
Q

Biliary Colic DDx

A

cholecystitis/ other gallstone disease
pancreatitis
bowel perforation

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7
Q

Biliary Colic Ix

A

Same work up as cholecystitis as may be difficult to
differentiate clinically.

Urine: bilirubin, urobilinogen, Hb
Bloods: FBC, U+E, amylase, LFTs, G+S, clotting, CRP

Imaging
 AXR: 10% of gallstones are radio-opaque
 Erect CXR: look for perforation
US:
 Stones: acoustic shadow
 Dilated ducts: >6mm
 Inflamed GB: wall oedema

If Dx uncertain after US
 HIDA cholescintigraphy: shows failure of GB filling
(requires functioning liver)
 If dilated ducts seen on US → MRCP

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8
Q

Biliary Colic Rx

A

Conservative
- Rehydrate +NBM
- opioid analgesia (morphing 5-10mg/2h max
high recurrence rate (surgical favoured)

Surgical

  • Urgent lap chole (same admission)
  • elective lap chole 6-12 weeks
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9
Q

Acute cholecystitis

Pathogenesis + sequelae

A

Pathogenesis
 Stone or sludge impaction in Hartmann’s pouch
 → chemical and / or bacterial inflammation
 5% are acalculous: sepsis, burns, DM

Sequelae

  1. Resolution ± recurrence
  2. Gangrene and rarely perforation
  3. Chronic cholecystitis
  4. Empyema
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10
Q

Acute cholecystitis Presentation + examination

A
Severe RUQ pain
- continuous 
- radiates to right scapula + epigastrium 
Fever 
Vomiting
O/E
Local peritonism in RUQ
Tachycardia c¯ shallow breathing
± jaundice
Murphy’s sign
 2 fingers over the GB and ask pt. to breath in
 → pain and breath catch. Must be –ve on the L
Phlegmon may be palpable
Mass of adherent omentum and bowel
Boas’ sign
 Hyperaesthesia below the right scapula
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11
Q

Murphy’s sign

A

Acute cholecystitis
 2 fingers over the GB and ask pt. to breath in
 → pain and breath catch. Must be –ve on the L

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12
Q

Phlegmon

A

Mass of adherent omentum and bowel

(acute cholecystitis)

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13
Q

Boas’ Sign

A

Hyperaesthesia below the right scapular

acute cholecystitis

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14
Q

Acute cholecystitis Ix

A

Urine: bilirubin, urobilinogen

Bloods
 FBC: ↑ WCC
 U+E: dehydration from vomiting
 Amylase, LFTs, G+S, clotting, CRP

Imaging
 AXR: gallstone, porcelain gallbladder
 Erect CXR: look for perforation
US
 Stones: acoustic shadow
 Dilated ducts (>6mm)
 Inflamed GB: wall oedema

If Dx uncertain after US
 HIDA cholescintigraphy: shows failure of GB
filling (requires functioning liver)
 MRCP if dilated ducts seen on US

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15
Q

Acute Cholecystitis Mx

A
Conservative
 NBM
 Fluid resuscitation
 Analgesia: paracetamol, diclofenac, codeine
 Abx: cefuroxime and metronidazole
 80-90% settle over 24-48h
 Deterioration: perforation, empyema

Surgical
 May be elective surgery @ 6-12wks (↓ inflam)
 If <72h, may perform lap chole in acute phase

Empyema
 High fever
 RUQ mass
 Percutaneous drainage: cholecystostomy

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16
Q

Chronic Cholecystitis Sx

A
Flatulent Dyspesia
Vague upper abdominal discomfort
Distension, bloating
Nausea
Flatulence, burping
Symptoms exacerbated by fatty foods
 CCK release stimulates gallbladder
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17
Q

Chronic Cholecystitis Ix + Mx

A

Ix
 AXR: porcelain gallbladder
 US: stones, fibrotic, shrunken gallbladder
 MRCP

Mx
Medical
 Bile salts (not very effective)

Surgical
 Elective cholecystectomy
 ERCP first if US shows dilated ducts and stones

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18
Q

Mucocele

A

Neck of gallbladder blocked by stone but contents
remains sterile
 Can be very large → palpable mass
 May become infected → empyema

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19
Q

Gallbladder Carcinoma

A

Rare
 Associated c¯ gallstones and gallbladder polyps.
 Calcification of gallbladder → porcelain GB
 Incidental Ca found in 0.5-1% of lap choles.

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20
Q

Mirizzi’s Syndrome

A

Rare
 Large stone in GB presses on the common hepatic duct
→ obstructive jaundice.
 Stone may erode through into the ducts

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21
Q

Gallstone Ileus

A
Large stone (>2.5cm) erodes from GB → duodenum
through a cholecysto-duodenal fistula 2ndary to chronic inflam.
May impact in distal ileum → obstruction

Rigler’s Triad:
 Pneumobiliia
 Small bowel obstruction
 Gallstone in RLQ

Rx: stone removal via enterotomy

NB. Bouveret’s syn. = duodenal obstruction

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22
Q

Obstructive Jaundice

A

33% stones
33% Ca head of the pancreas

33% Other
 LNs @ porta hepatis: TB, Ca
 Inflammatory: PBC, PSC
 Drugs: OCP, sulfonylureas, flucolox
 Neoplastic: Cholangiocarcinoma
 Mirizzi’s syndrome
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23
Q

Obstructive jaundice clinical features

A

Jaundice (noticeable at 50mM) - seen on tongue frenulum first

Dark urine, pale stools
Itch (Bile salts)

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24
Q

Obstructive Jaundice Ix

A

Urine -Dark
 ↑ bilirubin ↓ urobilinogen

Bloods
 FBC: ↑ WCC in cholangitis
 U+E: hepatorenal syndrome
 LFT: ↑cBR, ↑↑ ALP, ↑AST/ALT
 Clotting: ↓ vit K → ↑ INR
 G+S: may need ERCP
 Immune: AMA, ANCA, ANA

Imaging
AXR - May visualise stone
 Pneumobilia suggests gas forming infection

US
 Dilated ducts >6mm
 Stones (95% accurate)
 Tumour

MRCP or ERCP
Percutaneous Transhepatic Cholangiography

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25
Mx of stones in obstructive jaundice
``` Conservative  Monitor LFTs: passage of stone may → resolution  Vitamins ADEK  Analgesia  Cholestyramine ``` Interventional  If: no resolution, worsening LFTs or cholangitis  ERCP c¯ sphincterotomy and stone extraction Surgical Open / lap stone removal c¯ T tube placement  T tube cholangiogram 8d later to confirm stone removal. Delayed cholecystectomy to prevent recurrence
26
Ascending Cholangitis
May complicate CBD obstruction Charcot's Triad - fever/rigors, RUQ pain, jaundice Reynolds Pentad - Charcot's triad + confusion + shock
27
Ascending cholangitis Mx
Cef and met  1st: ERCP  2nd: Open or lap stone removal c¯ T tube drain
28
Charcot's triad
Fever/rigors, jaundice, RUQ pain Ascending cholangitis
29
Courvoisier's Law
Painless obstructive jaundice w a palpable gallbladder unlikely to be due to stones
30
Pancreatic Carcinoma RF + pathology
``` SINED Smoking Inflammation - chronic pancreatitis Nutrition (fatty diet) EtOH DM ``` ``` 90% ductal carinoma Presents late, mets early  Direct extension to local structures  Lymphatics  Blood → liver and lungs 60% head, 25% body, 15% tail ```
31
Pancreatic Carcinoma Presentation + signs
60+ M  Painless obstructive jaundice: dark urine, pale stools  Epigastric pain: radiates to back, relieved sitting forward  Anorexia, wt. loss and malabsorption  Acute pancreatitis  Sudden onset DM in the elderly Signs  Palpable gallbladder  Jaundice  Epigastric mass  Thrombophlebitis migrans (Trousseau Sign)  Splenomegaly: PV thrombosis → portal HTN  Ascites
32
Pancreatic Carcinoma Ix
Bloods: cholestatic LFTs, ↑Ca19-9 (90% sens), ↑Ca ``` Imaging  US: pancreatic mass, dilated ducts, hepatic mets, guide biopsy  EUS: better than CT/MRI for staging  CXR: mets  Laparoscopy: mets, staging ``` ERCP  Shows anatomy  Allows stenting  Biopsy of peri-ampullary lesions
33
Pancreatic Cancer Rx + Prognosis
``` Surgery  Fit, no mets, tumour ≤3cm (≤10% of pts)  Whipple’s pancreaticoduodenectomy  Distal pancreatectomy  Post-op chemo delays progression  5ys = 5-14% ``` Palliation  Endoscopic / percutaneous stenting of CBD  Palliative bypass surgery: – cholecystojejunostomy + gastrojejunostomy  Pain relief – may need coeliac plexus block Prognosis - mean survival <6mo - 5ys = <2%
34
Acute Pancreatitis Path
Pancreatic enzymes released and activated in vicious circle → multi-stage process. 1. Oedema + fluid shift + vomiting → hypovolaemic shock while enzymes → autodigestion and fat necrosis 2. Vessel autodigestion → retroperitoneal haemorrhage 3. Inflammation → pancreatic necrosis 4. Super-added infection: 50% of pts. c¯ necrosis 10% mortality
35
Acute pancreatitis causes
Idiopathic (20%) ?microstones Gallstones (45%) Ethanol (25%) Trauma ``` Steroids Mumps (other infections - Coxackie B) Autoimmune (PAN) Scorpion (trinidad) Hyperlipidaemia, hypercalcaemia, hypothermia ERCP - 5% risk Drugs - thiazides, azathioprine ```
36
Acute Pancreatitis Sx + Signs
Sx Severe epigastric pain → back  May be relieved by sitting forward Vomiting ``` Signs ↑HR, ↑RR, Fever Hypovolaemia → shock Epigastric tenderness Jaundice Ileus → absent bowel sounds Ecchymoses  Grey Turners: flank  Cullens: periumbilical (tracks up Falciform) ```
37
Grey Turner's
Flank ecchymoses acute pancreatitis
38
Cullen's
Periumbilical ecchymoses Tracks up falciform acute pancreatitis
39
Modified Glasgow Criteria
Valid for EtOH and Gallstones - Assess severity + predict mortality ``` PANCREAS  PaO2 <8kPa  Age >55yrs  Neutrophils >15 x109/L  Ca2+ <2mM  Renal function U>16mM  Enzymes LDH>600iu/L AST>200 iu/L  Albumin <32g/L  Sugar >10mM ``` ``` 1 = mild 2 = mod 3 = severe ```
40
Acute Pancreatitis Ix
``` Bloods FBC: ↑WCC ↑amylase (>1000 / 3x ULN) and ↑lipase  ↑ in 80%  Returns to normal by 5-7d U+E: dehydration and renal failure LFTs: cholestatic picture, ↑AST, ↑LDH Ca2+: ↓ Glucose: ↑ CRP: monitor progress, >150 ``` Urine: glucose, ↑cBR, ↓urobilinogen Imaging  CXR: ARDS, exclude perfed DU  AXR: sentinel loop, pancreatic calcification  US: Gallstones and dilated ducts, inflammation  Contrast CT: Balthazar Severity Score
41
Conservative Mx of Acute Pancreatitis
Manage @ appropriate level: e.g. ITU if severe  Constant reassessment is key  Hrly TPR, UO  Daily FBC, U+E, Ca2+, glucose, amylase ABG Fluid resus - aggressive - keep UO>30ml/h Catheter +/- CVP Pancreatic rest NBM, NGT if vomiting, poss TPN to prevent catabolism Analgesia - pethidine via PCA, or morphine 5-10mg/2h max Abx - not routine if mild, use if suspicion of infection or before ERCP - Penems (meropenem, imipenem)
42
Conservative Mx Complications of Acute Pancreatitis
``` Mx Complications  ARDS: O2 therapy or ventilation  ↑ glucose: insulin sliding scale  ↑/↓Ca  EtOH withdrawal: chlordiazepoxide ```
43
Interventional Mx of Acute Pancreatitis
ERCP (Endoscopic Retrograde Cholangio-Pancreatography) If pancreatitis w dilated ducts 2ndary to gallstones ERCP + sphincterectomy > less complications Surgical Mx - infected pancreatic necrosis - pseudocyst or abscess - unsure Dx Operations  Laparotomy + necrosectomy (pancreatic debridement)  Laparotomy + peritoneal lavage  Laparostomy: abdomen left open c¯ sterile packs in ITU
44
Early Complications of Acute Pancreatitis
``` Early: Systemic Respiratory: ARDS, pleural effusion Shock: hypovolaemic or septic Renal failure DIC ``` Metabolic  ↓ Ca2+  ↑ glucose  Metabolic acidosis
45
Late Complications of Acute Pancreatitis
``` Late (>1wk): Local Pancreatic necrosis Pancreatic infection Pancreatic abscess May form in pseudocyst or in pancreas Open or percutaneous drainage Bleeding: e.g. from splenic artery May require embolisation ``` Thrombosis - Splenic A., GDA or colic branches of SMA  May → bowel necrosis -Portal vein → portal HTN Fistula formation  Pancreato-cutaneous → skin breakdown
46
Pancreatic Pseudocyst
Collection of pancreatic fluid in the lesser sac surrounded by granulation tissue Occur in 20% (esp. in EtOH pancreatitis) Presentation  4-6wks after acute attack  Persisting abdominal pain  Epigastric mass → early satiety Complications  Infection → abscess  Obstruction of duodenum or CBD Ix  Persistently ↑ amylase ± LFTs  US / CT ``` Rx <6cm: spontaneous resolution >6cm  Endoscopic cyst-gastrostomy  Percutaneous drainage under US/CT ```
47
Chronic Pancreatitis Causes
``` AGITS Alcohol (70%) Genetic - CF, HH Immune - Lymphoplasmacytic sclerosing pancreatitis (↑IgG4) Triglycerides ↑ Structural  Obstruction by tumour  Pancreas divisum ```
48
Chronic Pancreatitis Presentation
``` Epigastric Pain  Bores through to back  Relieved by sitting back or hot water bottle → erythema ab igne  Exacerbated by fatty food or EtOH ``` Steatorrhoea and wt. loss DM: polyuria, polydipsia Epigastric mass: pseudocyst
49
Chronic Pancreatitis Ix
``` ↑ glucose ↓ faecal elastase: ↓ exocrine function US: pseudocyst AXR: speckled pancreatic calcifications CT: pancreatic calcifications ```
50
Chronic Pancreatitis Rx
Diet  No EtOH  ↓ fat, ↑ carb ``` Drugs  Analgesia: may need coeliac plexus block  Enzyme supplements: pancreatin (Creon)  ADEK vitamins  DM Rx ``` Surgery Indications  Unremitting pain  Wt. loss  Duct blockage Procedures  Distal pancreatectomy, Whipple’s  Pancreaticojejunostomy: drainage  Endoscopic stenting
51
Chronic Pancreatitis Complications
``` Pseudocyst DM Pancreatic Ca Pancreatic swelling → biliary obstruction Splenic vein thrombosis → splenomegaly ```
52
Pancreatic Insulinoma
> fasting/exercise-induced hypoglycaemia Confusion,stupor, LOC ↑ insulin + ↑ c-peptide + ↓glucose
53
Pancreatic Gastrinoma
Zollinger-Ellison Hypergastrinaemia → hyperchlorhydria → PUD and chronic diarrhoea (inactivation of pancreatic enzymes)
54
Pancreatic Glucagonoma
↑ se glucagon → mild DM Characteristic blistering rash  Necrolytic migratory erythema
55
Pancreatic VIPoma
Verner-Morrison XS VIP Watery Diarrhoea Hypokalaemia Achlorhydria Acidosis
56
Somatostatinoma
Somatostatin - inhibits glucagon + insulin release - inhibits pancreatic enzyme secretion Features - DM - Steatorrhoea - Gall stones usually v malignant > poor progn
57
Pancreatic Malformations
Ectopic Pancreas - Meckel's diverticulum - Small Bowel
58
Pancreas Divisum
Failure of fusion of dorsal and ventral buds → bulk of pancreas drains through smaller accessory duct. Usually asymptomatic May → chronic pancreatitis
59
Annular Pancreas
Fusion of dorsal and ventral buds around duodenum |  May present c¯ infantile duodenal obstruction.
60
Cholangiocarcinoma Path + RF
Rare bile duct tumouir Adenocarcinoma Typically at confluence of R+L heaptic ducts (Klatskin tumours) ``` RF Primary Sclerosing Cholangitis Ulcerative colitis Choledocholithiasis Hep B/C Choledochal cysts Lynch 2 Flukes ```
61
Cholangiocarcinoma Presentation Ix Rx
Progressive painless obstructive jaundice  Gallbladder not palpable Steatorrhoea Wt. loss Ix  Cholestatic LFTs  CA 19-9 Rx  Poor prognosis: no curative Rx  Palliative stenting by ERCP
62
Hydatid Cyst
Zoonotic infection by Echinococcus granulosus  Occurs in sheep-rearing communities  Parasite penetrates the portal system and infects the liver → calcified cyst Presentation Mostly asymptomatic 2ndary infection Pressure effects  Non-specific pain  Abdominal fullness  Obstructive jaundice ``` Rupture  Biliary colic  Jaundice  Urticaria  Anaphylaxis ``` Ix - eosinophilia, CT Rx - Medical - albendazole Surgical - cystectomy (for large cysts)