PE - Approach to Hepatomegaly Flashcards

1
Q

Outline the parameters to report in the abdominal examination

A

1) Nutrition state (cachectic or well-nourished)
2) Stigmata of chronic liver disease
3) Presence of conjunctival pallor and scleral jaundice
4) Lymphadenopathy
5) Abdominal distension
6) Clinical evidence of ascites
7) Hepatomegaly (size) + tender/non-tender + edge/surface
8) Absence of splenomegaly
9) Presence of umbilical nodule (Sister Mary Joseph)
10) Brutis or venous hum
11) Signs of encephalopathy to suggest liver failure

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2
Q

List differentials for tender hepatomegaly

A

1) Infectious (HBV, HCV, EBV, CMV, HHV-6, HIV, toxoplasmosis)
2) Alcoholic hepatitis
3) Malignancy including hematological
4) Hepatic congestion secondary to heart failure
5) Vascular liver disease (e.g. Budd-Chiari, sickle cell)

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3
Q

Outline what temporalis wasting indicates

A

Temporalis wasting is an early sign of generalized muscle atrophy

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4
Q

Outline the clinical significance of anemia

A

1) Chronic liver disease
2) Hematological malignancy
3) Malignancy
4) Hematological disease e.g. sickle cell disease

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5
Q

Define the normal liver span based on sex

A
Men = less than 10.5cm
Women = less than 7cm
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6
Q

Outline the clinical significance of Sister Mary Joseph nodule

A

Metastatic deposit found in the following malignancies

1) Hepatocellular carcinoma
2) Colorectal adenocarcinoma
3) Gastric adenocarcinoma
4) Lymphoma

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7
Q

Describe the hepatic venous hum

Outline its clinical significance

A

Continuous murmur best heard over the epigastrium indicative of portal HT

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8
Q

Outline the clinical significance of hepatic encephalopathy

A

Hepatic encephalopathy tends to occur more in acute liver decompensation rather than chronic liver disease so consider acute causes of liver failure

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9
Q

If malignancy is a top differential after completing the examination what should be the next step?

A

Consider both primary and secondary malignancies so assess other systems to look for primary tumours

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10
Q

When is the jugular venous pressure relevant in abdominal examination?

A

1) Presence of ascites

2) Presence of hepatomegaly

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11
Q

Explain why the jugular venous pressure is relevant in abdominal examination if the patient has ascites or hepatomegaly

A

1) Cirrhosis is a state of systemic vasodilation so cardiac filling pressure is either low or normal thus JVP should be normal
2) If JVP is elevated then there is likely right heart failure causing hepatic congestion which may induce hepatomegaly w/ascites
3) Palpate the liver for pulsatile hepatomegaly in cases w/tricuspid regurgitation

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12
Q

List the cause of isolated hepatomegaly

A

1) Cirrhosis
1. Alcoholic fatty liver disease
2. Non-alcoholic steatohepatitis (NASH)
3. Primary biliary cirrhosis (PBC)
2) Malignancy (primary and secondary)
3) Infectious disease
1. HBV/HCV/HAV/HEV
2. EBV/CMV/HHV-6
3. HSV
4. Toxoplasmosis
5. Pyogenic liver abscess
6. Amoebic liver abscess
7. Hydatid disease
4) Infiltrative disease
1. Amyloidosis
2. Sarcoidosis
3. Glycogen storage disorders
5) Vascular liver disease
1. Budd-Chiari syndrome
2. Sickle cell disease
6) Polycystic liver disease
7) Tertiary syphilis (syphilitic gumma)

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13
Q

List the tumours that commonly metastasize to the liver

A

Colorectal most common!!!

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14
Q

List bengin liver tumours

A

1) Cavernous hemangioma = most common benign tumour; typically in women of childbearing age
2) Hepatic adenoma = associated w/use of estrogen containing contraceptives
3) Focal nodular hyperplasia = affects women of childbearing age w/no association to estrogen use
4) Nodular regenerative hyperplasia = elderly patients w/systemic autoimmune disease

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15
Q

List the infective causes of acute hepatitis

A

1) HBV
2) HCV
3) HAV
4) HEV
5) EBV
6) CMV
7) HSV
8) Toxoplasmosis

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16
Q

Define Budd-Chiari syndrome

A

Hepatic venous outflow obstruction

  • obstruction commonly by thrombosis
  • obstruction may occur at hepatic venules, hepatic vein, or IVC
  • results in venous stasis, congestion, and damage to hepatic parenchymal cells
17
Q

Describe the clinical presentation of Budd-Chiari syndrome

A

1) Subacutely w/abdominal pain + hepatomegaly
2) Acutely w/jaundice + hepatic encephalopathy

Ascites can be absent if there is adequate hepatic venous collateral circulation

18
Q

Outline the diagnosis of Budd-Chiari syndrome

A

1) Doppler USG of hepatic vein

19
Q

List the causes of Budd-Chiari syndrome

A

75% of cases have an identifiable underlying cause

1) Myeloproliferative disorders
2) Thrombophilias
- protein C deficiency
- protein S deficiency
- antithrombin III deficiency
- Factor V Leiden mutation
- prothrombin gene mutation
3) Antiphospholipid syndrome
4) Paroxysmal nocturnal hemoglobinuria

20
Q

Outline the treatment of Budd-Chiari syndrome

A

No encephalopathy or hepatic failure = anticoagulate + medical management of ascites

Encephalopathy or hepatic failure = thrombolysis + angioplasty ± liver transplant

21
Q

List the hepatic manifestations of sickle cell disease

A

1) Gallstone disease
- pigment stones from chronic hemolysis

2) Sickle hepatic crisis
- sickle thrombosis causing sinusoidal obstruction
- triad of RUQ + jaundice + hepatomegaly
- do not confuse w/Charcot’s triad for cholangitis of RUQ + jaundice + fever ± Reynold’s pentad confusion + hypotension

3) Intrahepatic cholestasis
- sickle thrombosis causing sinusoidal obstruction
- induces hepatocyte swelling and intrahepatic biliary obstruction

4) Fe overload from repeated blood transfusion
5) Blood borne disease from blood transfusion