Abdominal Flashcards

0
Q

Causes of CLD

A

Commonest = alcohol + viral
Toxins: alcohol, drugs (amiodarone, methotrexate)
Viral: hepB, hepC, CMV, EBV
Metabolic: non-alcoholic steatohepatitis, haemochromatosis, wilsons, alpha-1-antitrip
Autoimmune: AIH, PBC, PSC
Neoplasm: HCC, mets
Vasc: Budd-Chiari, RHF

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1
Q

CLD complications

A

Portal hypertension (ascites, hypersplenism, varices)
Synthetic dysfunction (albumin, clotting)
Hepatic encephalopathy
Hepatorenal
Hepatopulomary
HCC

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2
Q

Hepatosplenomegaly causes

A
Portal HTN
CML
Non-Hodgkins lymphoma
Infective endocarditis
Myelofibrosis
Infiltration (amyloidosis)
Granulomatous disease (TB, sarcoid, wegeners)
Other infectious (malaria, kala-azar, schisto)
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3
Q

Hepatomegaly causes

A
Cirrhosis
CCF
Neoplastic (Mets and primary)
Infective: acute viral, liver abscess
Polycystic disease
Tricuspid regurg
Budd-Chiari
Haemochromatosis
Infiltration: amyloidosis, sarcoidosis
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4
Q

Splenomegaly causes

A
Cirrhosis with portal hypertension
Myeloproliferative: CML, myelofibrosis
Lymphoma
Infections: endocarditis, EBV, CMV, malaria, kala-azar
SLE, RA, scleroderma, sarcoidosis
Haemolytic anaemias
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5
Q

Causes of asterixis

A

Hepatic encephalopathy
Uraemia
Hypercapnea
Electrolytes: hypoglycaemia, hypokalaemia, hypoMg
Drug intoxication: barbiturates, phenytoin, alcoholism

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6
Q

Precipitants of hepatic encephalopathy

A

Increased nitrogen: constipation, GI bleed, blood transfusion, infection, hypokalaemia
Decreased toxin clearance: dehydration, hypotension, anaemia, portosystemic shunts
Altered neurotransmission: benzos, psychoactive drugs
Hepatocellular damage: continued alcohol use, HCC

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7
Q

Examination findings of encephalopathy

A
Confusion
Hyper-reflexia
Rigidity
Asterixis
Myoclonus
Hippus (rhythmic dilation/constriction of pupil)
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8
Q

PBC associated AI conditions

A

RA, thyroid, Sjögrens, scleroderma, SLE, coeliac

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9
Q

PBC treatment

A

Ursodeoxycholic acid or cholestyramine.

Liver transplant

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10
Q

What does haemochromatosis affect?

A
Liver
Joints
Heart
Skin
Endocrine
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11
Q

Wilsons diagnostic tests

A

Low serum copper and caeruloplasmin
High 24-hour urinary copper
Gold standard is liver biopsy
ATP7B gene analysis

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13
Q

Wilson’s disease management

A

D-penicillamine and trientine promote excretion

Penicillium in not used for neuropsych symptoms, use zinc salts instead and for presymptomatic patients

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14
Q

Causes of ascities

A
Cirrhosis
CCF/RHF
Intra-abdominal malignancy
Hypoalbuminaemia
Uncommon (nephrotic syn, TB, chylous)
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15
Q

Causes of portal hypertension

A

Pre-hepatic: thrombosis
Hepatic: cirrhosis
Post-hepatic: Cardiac (RHF, TR), Budd-Chiari

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16
Q

Ascites treatment

A
Treat underlying condition, daily weights, fluid + salt restrict, diruetics (spiro).
Therapeutic paracentesis (give HAS)
If diuretic-resistant - shunting (TIPS, peritoneovenous) or transplant
17
Q

Jaundice causes

A

Commonest = Haemolysis, CLD, gallstones
Pre-hepatic: haemolysis (AIHA, HS, SCD, G6PD, malaria)
Hepatic: CLD, Hepatitis (EtOH, viral), Drugs (para, statins, anti-TB), Congential, AIH, Ca
Post-hepatic: Gallstones, Panc Ca, PBC, PSC, cholestasis (OCP, augmentin)

18
Q

Differential for Mercedes Benz Scar

A

Hepatobiliary surgery

  • Liver transplant
  • Segmental resection
  • Whipples’: pancreaticoduodenectomy
19
Q

Differential for bilateral renal enlargement

A
APKD
Bilateral hydronephrosis
Amyloidosis
Tuberous sclerosis
Von-Hippel-Lindae disease
20
Q

APKD associations

A

Liver, splenic, pancreatic cysts
Heart: mitral valve prolapse, AR
Intracranial aneurysms
Colonic diverticula, abdo hernias

21
Q

Common causes of CKD

A
DM
GN e.g. IgA nephropathy
Reflux nephropathy
Obstructive nephropathy
Renovascular disease
Hypertension
Polycystic kidney disease