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HOW TO DIAGNOSE THE
CAUSE OF JAUNDICE?

MIM.ILHAM
4th Batch
FHCS,EUSL
Contents
•
•
•
•
•

Bilirubin metabolism.
Causes of Jaundice
History
Examination
Special test.
Bilirubin metabolism.
Causes of Jaundice
Causes of Jaundice
• Increased bilirubin load (Haemolytic Jaundice)
1.
2.
3.
4.
5.
6.
7.
8.

Hereditary spherocytosis
Hereditary non spherocytic anaemia
Sickle cell disease
Thalassemia
Acquired haemolytic anaemia
Incompatible blood transfusion
Severe sepsis
Drugs
Causes of Jaundice
• Disturbed bilirubin uptake and conjugation of
bilirubin
1.
2.
3.
4.
5.
6.

Viral hepatitis
Hepatotoxins
Cirrhosis
Gilbert’s familial hyperbilirubinaemai (AD)
Familial neonatal hyperbilirubinaemia
Crigler-Najjar’s familial jaundice (Type1- AR, Type2AD)
Causes of Jaundice
• Disturbed bilirubin excretion
Excess of conjugated serum bilirubin known as cholestasis

Intra hepatic (without mechanical obstruction)
1.
2.
3.
4.
5.
6.

Cirrhosis
Viral (chronic active) hepatitis.
Drugs- chorpromazine, methyl testosterone
Dubin-Johnson’s familial hyperbilirubinaemia(AR)
Primary biliary cirrhosis
Parenteral or enteral feeding with synthetic
nutrition
Causes of Jaundice
Extra hepatic cholestasis
• Inside the duct
1. Gallstones
2. Foreign body eg- Broken T-tube, parasites
(Hydatid,liver fluke, round worms)
• In duct wall
1. Congenital atresia
2. Traumatic stricture
3. Sclerosing cholangitis
4. Tumor of the bile duct
Causes of Jaundice
• Outside duct
1. Carcinoma of head of the pancreas
2. Carcinoma of the ampulla
3. Pancreatitis
4. Lymph node metastases
History
Age:
• Young age- Hepatitis is common
• Old age- Malignancy (CA) is common
History
PC:
• Jaundice (Yellowish discoloration of
sclera+mucus membrane+Skin)
• Exclude other causes for yellow discolouration
*Carotenaemia (Only skin, mainly palm and sole
are orange color) in eating carrot,mango,papaya
and hypothyroidism
*Antimalarial drugs
*Vit-B12 deficiency
History
HPC & Systemic Rvw
• Jaundice
1. Sudden onset- Gall stones OR Viral hepatitis
2. Gradual onset- Cirrhosis, Pancreatic CA OR
Porta hepatis metastases
3. Progressive- Malignant obstruction
4. Fluctuaing- Stones in the CBD, CA of the
duodenal papilla OR repeated hemolytic
episodes.
History
• Pain:
1. Painless- Viral hepatitis (Dragging subcostal ache
due to hepatic enlargement)
2. Pailess+Fluctuating- intermittent obstruction by
gallstone OR necrosing ampullary CA
3. Painless+Progressive- Malignant obstruction of
CBD
4. Painful- Gallstones OR Pancreatic CA
Biliary colic- right subcosatl pain radiating beneath
the costal margin to shoulder blade
Moderate boring pain passing through to backChronic pancreatitis OR pancreatic tumor
History
• Fever:
1. Fever with chills- Extra hepatic cholestasis with
cholangitis due to bile duct stone,Liver abscess
and leptospirosis
2. Fever without chills- Viral hepatitis, Drug
induced hepatitis
• Pruritus:
Results from the irritation of cutaneous nerves by
retained bile salt
Cholestatic jaundice
History
• Weight lossProgressive weight loss- Malignancy
Also in chronic hepatocellular damage.
• Anorexia and fatigue
Early signs of hepatitis
(This is due to production of cachexin and TNF)
History
• Colour of the urine and stool
Pre hepatic

Hepatic

Post hepatic

Urine colour

Normal

Dark

Dark

Stool colour

Normal

Normal

Pale
History
Contact history:
1. Contact with jaundice patients from work
mates, family- hygienic habits such as toilets,
drinking water, taking meals from out side
(HepA & HepB)
2. Contact Hx of muddy water in leptospirosis
History
 Obstetric Hx:
• Ask about LRMP and calculate POA
• Benign intra hepatic cholestasis is common in
pregnancy period
History
PMHx
• Viral hepatitis
• History of transfusion of blood OR blood
products (HepB & HepC)
• Recent parenteral injection (HepB & HepC)
• Amoebic dysentery
• Jaundice following febrile illness- some
congenital haemolytic anaemia may be
triggered by febrile illness eg- G6PD deficiency
History
• Recurrent left hypochondrial pain due to
splenomegaly eg- Hereditary spherocytosis
• Recurrent foot ulcer eg- some form of chronic
haemolytic anaemia such as sickle cell disease
• Hx of breast cancer and bowelcancer
• SLE and other connective tissue disorders (Hx
suggestive of joint pain, skin rash)
History
PSHx
• Previous difficult biliary surgery suggest –
traumatic stricture OR a residual stones in the
CBD
• Post operative jaundice
1. Resorption of haematomas,haemoperitonium,
haemolysis of transfused erythrocyte
2. Impaired hepatocellular function- halogenated
anaesthetics, sepsis
History
DRUG Hx:
• Smilar to pre-hepatic jaundice- rifampicin,
methyldopa
• Intra-hepati jaundice- ethanol (cirrhosis ),
paracetamol, halothane, methyldopa,
barbiturates
• Post-hepatic jaundice- isoniazid, chlorpromazine
• Antileprosy drugs and Antipsychotic drugs
• OCP,Saliclate,Sulfonamide , MAOi
History
Family Hx:
• FHx of jaundice+anaemia+splenectomyHereditary spherocytosis
• FHx of jaundice+anaemia- congenital
hyperbilirubinaemias
• Consanguinity of parents- Inherited congenital
haemolytic anaemia eg- G6PD deficiency
• Neuropsychiatry llness+jaundice- Wilson’s
disease
History
 Social Hx:
• Hx of Alcohol consumption in Units for yearsChronic alcohol liver disease Hepatocellular CA
jaundice
Cirrhosis and pancreatic CA
• Toddy consumption- Amoebic liver abscess
• Sexual promiscuity and unprotected sexual behaviorHepB transmission
• Occupational HxSheep farmers OR allied workers- Hydatid infestation
Working at chemical enviorment eg-CCl4
Examination
 General:
• Depth of jaundice:
Lemmon yellow- haemolytic jaundice
Orange- hepatocellular cause
Deep mahogany hue- Prolonged obstructive
jaundice
Examination
• Anaemia:
Suggestive of Haemolytic,malignant OR cirrhotic
causes
Examination
• Liver failure
Examination
• Supraclavicular node enlargementMetastatic CA
• SkinScratches and xanthomas in chronic cholestasis
Examination
• PyrexiaCholangitis, Viraemia and hepatic involvement
eg-Infectious mononucleosis, septicaemia and
haemolysis and hepatic abscess
Examination
Abdominal Ex:
• Scars: previous surgery of biliary tree
Examination
• Caput medusae
Dilated periumblical vein indicatye portal HT and
cirrhosis
Examination
• Site of tenderness:
Tenderness over the gall bladder indicate biliary
inflammation
Examination
• Gall bladder
A palpable gall bladder in the presence of the
jaundice means that janundice is unlikely to be
due to a stone (Courvoisier’s sign). CA of head of
the pancreas must be suspected
Examination
• Liver:
1. Palpable large nodule of large proportionmetastatic malignancy
2. Small nodules- cirrhosis
3. Slightly enlarged smooth live chronic
cholestasis
4. Tender liver- viral hepatitis and liver abscess
Examination
• Spleen:
Splenomegaly may be evident of congenital
haemolytic anaemia
Examination
• Abdominal mass
Hard and irregular abdominal mass suggestive
of malignancy.
• Ascites
Due to abdominal malignancy or liver failure
Examination
• Rectal Ex
Colour of the stool
Presence of a primary malignancy or metastatic
deposit in the pouch of douglas

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How to Diagnose the Cause of Jaundice

  • 1. HOW TO DIAGNOSE THE CAUSE OF JAUNDICE? MIM.ILHAM 4th Batch FHCS,EUSL
  • 2. Contents • • • • • Bilirubin metabolism. Causes of Jaundice History Examination Special test.
  • 4.
  • 6. Causes of Jaundice • Increased bilirubin load (Haemolytic Jaundice) 1. 2. 3. 4. 5. 6. 7. 8. Hereditary spherocytosis Hereditary non spherocytic anaemia Sickle cell disease Thalassemia Acquired haemolytic anaemia Incompatible blood transfusion Severe sepsis Drugs
  • 7. Causes of Jaundice • Disturbed bilirubin uptake and conjugation of bilirubin 1. 2. 3. 4. 5. 6. Viral hepatitis Hepatotoxins Cirrhosis Gilbert’s familial hyperbilirubinaemai (AD) Familial neonatal hyperbilirubinaemia Crigler-Najjar’s familial jaundice (Type1- AR, Type2AD)
  • 8. Causes of Jaundice • Disturbed bilirubin excretion Excess of conjugated serum bilirubin known as cholestasis Intra hepatic (without mechanical obstruction) 1. 2. 3. 4. 5. 6. Cirrhosis Viral (chronic active) hepatitis. Drugs- chorpromazine, methyl testosterone Dubin-Johnson’s familial hyperbilirubinaemia(AR) Primary biliary cirrhosis Parenteral or enteral feeding with synthetic nutrition
  • 9. Causes of Jaundice Extra hepatic cholestasis • Inside the duct 1. Gallstones 2. Foreign body eg- Broken T-tube, parasites (Hydatid,liver fluke, round worms) • In duct wall 1. Congenital atresia 2. Traumatic stricture 3. Sclerosing cholangitis 4. Tumor of the bile duct
  • 10. Causes of Jaundice • Outside duct 1. Carcinoma of head of the pancreas 2. Carcinoma of the ampulla 3. Pancreatitis 4. Lymph node metastases
  • 11. History Age: • Young age- Hepatitis is common • Old age- Malignancy (CA) is common
  • 12. History PC: • Jaundice (Yellowish discoloration of sclera+mucus membrane+Skin) • Exclude other causes for yellow discolouration *Carotenaemia (Only skin, mainly palm and sole are orange color) in eating carrot,mango,papaya and hypothyroidism *Antimalarial drugs *Vit-B12 deficiency
  • 13. History HPC & Systemic Rvw • Jaundice 1. Sudden onset- Gall stones OR Viral hepatitis 2. Gradual onset- Cirrhosis, Pancreatic CA OR Porta hepatis metastases 3. Progressive- Malignant obstruction 4. Fluctuaing- Stones in the CBD, CA of the duodenal papilla OR repeated hemolytic episodes.
  • 14. History • Pain: 1. Painless- Viral hepatitis (Dragging subcostal ache due to hepatic enlargement) 2. Pailess+Fluctuating- intermittent obstruction by gallstone OR necrosing ampullary CA 3. Painless+Progressive- Malignant obstruction of CBD 4. Painful- Gallstones OR Pancreatic CA Biliary colic- right subcosatl pain radiating beneath the costal margin to shoulder blade Moderate boring pain passing through to backChronic pancreatitis OR pancreatic tumor
  • 15. History • Fever: 1. Fever with chills- Extra hepatic cholestasis with cholangitis due to bile duct stone,Liver abscess and leptospirosis 2. Fever without chills- Viral hepatitis, Drug induced hepatitis • Pruritus: Results from the irritation of cutaneous nerves by retained bile salt Cholestatic jaundice
  • 16. History • Weight lossProgressive weight loss- Malignancy Also in chronic hepatocellular damage. • Anorexia and fatigue Early signs of hepatitis (This is due to production of cachexin and TNF)
  • 17. History • Colour of the urine and stool Pre hepatic Hepatic Post hepatic Urine colour Normal Dark Dark Stool colour Normal Normal Pale
  • 18. History Contact history: 1. Contact with jaundice patients from work mates, family- hygienic habits such as toilets, drinking water, taking meals from out side (HepA & HepB) 2. Contact Hx of muddy water in leptospirosis
  • 19. History  Obstetric Hx: • Ask about LRMP and calculate POA • Benign intra hepatic cholestasis is common in pregnancy period
  • 20. History PMHx • Viral hepatitis • History of transfusion of blood OR blood products (HepB & HepC) • Recent parenteral injection (HepB & HepC) • Amoebic dysentery • Jaundice following febrile illness- some congenital haemolytic anaemia may be triggered by febrile illness eg- G6PD deficiency
  • 21. History • Recurrent left hypochondrial pain due to splenomegaly eg- Hereditary spherocytosis • Recurrent foot ulcer eg- some form of chronic haemolytic anaemia such as sickle cell disease • Hx of breast cancer and bowelcancer • SLE and other connective tissue disorders (Hx suggestive of joint pain, skin rash)
  • 22. History PSHx • Previous difficult biliary surgery suggest – traumatic stricture OR a residual stones in the CBD • Post operative jaundice 1. Resorption of haematomas,haemoperitonium, haemolysis of transfused erythrocyte 2. Impaired hepatocellular function- halogenated anaesthetics, sepsis
  • 23. History DRUG Hx: • Smilar to pre-hepatic jaundice- rifampicin, methyldopa • Intra-hepati jaundice- ethanol (cirrhosis ), paracetamol, halothane, methyldopa, barbiturates • Post-hepatic jaundice- isoniazid, chlorpromazine • Antileprosy drugs and Antipsychotic drugs • OCP,Saliclate,Sulfonamide , MAOi
  • 24. History Family Hx: • FHx of jaundice+anaemia+splenectomyHereditary spherocytosis • FHx of jaundice+anaemia- congenital hyperbilirubinaemias • Consanguinity of parents- Inherited congenital haemolytic anaemia eg- G6PD deficiency • Neuropsychiatry llness+jaundice- Wilson’s disease
  • 25. History  Social Hx: • Hx of Alcohol consumption in Units for yearsChronic alcohol liver disease Hepatocellular CA jaundice Cirrhosis and pancreatic CA • Toddy consumption- Amoebic liver abscess • Sexual promiscuity and unprotected sexual behaviorHepB transmission • Occupational HxSheep farmers OR allied workers- Hydatid infestation Working at chemical enviorment eg-CCl4
  • 26. Examination  General: • Depth of jaundice: Lemmon yellow- haemolytic jaundice Orange- hepatocellular cause Deep mahogany hue- Prolonged obstructive jaundice
  • 27. Examination • Anaemia: Suggestive of Haemolytic,malignant OR cirrhotic causes
  • 29. Examination • Supraclavicular node enlargementMetastatic CA • SkinScratches and xanthomas in chronic cholestasis
  • 30. Examination • PyrexiaCholangitis, Viraemia and hepatic involvement eg-Infectious mononucleosis, septicaemia and haemolysis and hepatic abscess
  • 31. Examination Abdominal Ex: • Scars: previous surgery of biliary tree
  • 32. Examination • Caput medusae Dilated periumblical vein indicatye portal HT and cirrhosis
  • 33. Examination • Site of tenderness: Tenderness over the gall bladder indicate biliary inflammation
  • 34. Examination • Gall bladder A palpable gall bladder in the presence of the jaundice means that janundice is unlikely to be due to a stone (Courvoisier’s sign). CA of head of the pancreas must be suspected
  • 35. Examination • Liver: 1. Palpable large nodule of large proportionmetastatic malignancy 2. Small nodules- cirrhosis 3. Slightly enlarged smooth live chronic cholestasis 4. Tender liver- viral hepatitis and liver abscess
  • 36. Examination • Spleen: Splenomegaly may be evident of congenital haemolytic anaemia
  • 37. Examination • Abdominal mass Hard and irregular abdominal mass suggestive of malignancy. • Ascites Due to abdominal malignancy or liver failure
  • 38. Examination • Rectal Ex Colour of the stool Presence of a primary malignancy or metastatic deposit in the pouch of douglas