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Gastroenterology
Hepatomegaly
• Liver
– Malignancy – hepatoma/ metastases
– Infection – Hepatitis, abscess, typhoid
– Alcohol – fatty liver
• Non liver causes
– Congestive heart failure
– Hemolytic anaemia, myeloproliferative disorder
(leukemia)
– Autoimmune
• Others
– Wilson disease (rare)
Splenomegaly
• C ongestion- congestive heart failure, portal hpt
• H emolytic anemia – Thal, heriditary spherocytosis
• I nfection
– Bacteria : IE, typhoid
– Viral : IM, CMV
– Parasite : malaria
– Fungal
• N eoplasm – myeloproliferative/ lymphoproliferative
• A utoimmune - CTD
ascites
Classified by serum ascites to albumin concentration gradient
High gradient (>11g/L)
1.Cirrhosis
2.Budd chiari syndrome
3. Alholic hepatitis
4. Fulminant hepatic failure
5. Congestive heart failure, contrictive pericarditis (cardiac ascites)
6. Myxedema
Low gradient (<11gL)
1. Peritoneal ascites
2. Tb
3. Pancreatic ascites
4. Nephrotic syndrome
*serum-ascitic albumin gradient (SAAG) = serum
albumin value- ascitic fluid albumin value
High gradient (TRANSUDATIVE)= incr hydrostatic
pressure within blood vessels of hepatic portal
system, pushes the fluid into peritoneal cavity,
leaving protein such as albumin in the serum
Low gradient (EXUDATIVE)= not associated with
portal pressure
• Transudate – dt incr hydrostatic pressure, red
oncotic pressure, Na+ retention. Low protein
• Exudate – incr permeability of vessels,
lymphatic obstruction. Rich in protein
cirrhosis
Definition
-Necrosis of liver cell>nodule formation& fibrosis
-Abnormal liver architecture & liver blood flow and function
-Produce clinical features of portal hpt and impaired liver cell fx
Causes
#Common- hep(c or b+/-d), alcohol or non alcoholic fatty liver ds
#others: biliary cirrhosis, autoimmune hep, budd chiari, {heriditary
haemochromatosis, wilson)
Pathogenesis
Activation of stellate cells>proliferation of fibroblast>deposition of collagen
Pathology
-Characteristic features: regenerating nodules sep by fibrous septa. Loss of N
architecture within nodules.
-2 types: micro & macronodular cirrhosis
Micro Macro
Ongoing alcohol damage chr viral hep
Biliary tract ds
Symptoms
-R hypochondriac pain
-abd distension
-ankle swelling
-hematemesis and malena (varices dt portal hpt causing
GI bleed)
-pruritus (skin-cholestasis dt primary biliary cirrhosis)
-gynaecomastia, loss of libido, amenorrhea (endocrine
dysfunction)
-confusion and drowsiness (neuropsychiatric
manifestation dt portosystemic encephalopathy)
Signs
Periphery
-dupuytren contracture (alcoholic cirrhosis)
-clubbing
-palmar erythema (hyperdynamic circ also seen in pregnancy, thyrotoxicosis, RA)
-xanthoma(cholesterol deposits in palmar crease or above eyes dt primary biliary
cirrhosis)
Face, Neck, chest
-xanthelasma
-parotid gland enlarge
-spider naevi (>5 diagnostic, svc distribution, telengiectasia consist of central
arteriole and radiating small vessels)
-gynaecomastia
Abdomen
-Hepatomegaly>shrink in established cirrhosis
-Splenomeglay(portal hpt)
Endocrine
Gynaecomastia
Testicular atrophy
Ix
1. Severity-LFT(low serum albumin, prolong PT, incr
ALP and ALT, if decompesated CLF all will
deranged), BUSE (low sodium, high cr >130
worse prognosis)
2. Types: viral serology, autoAb, ig, iron& ferritin,
copper&ceruloplasmin, alpha1 antitrypsin
3. Imaging – Abd USS, CT(arterial-hcc, portal-
metastases, av- haemangioma), endoscopy
(varices/portal hypertensive gastropathy), MRI
4. Liver biopsy
Budd-chiari syndrome
Definition
Obestruction of venous outflow of liver
Dt occlusion of haptic veins
Causes
-1/3 unknown
-hypercoagulability state (polycythaemia vera, paroxysmal
nocturnal haemoglobinuria)
-thrombophilia
-ocp
-leukemia
-others: HCC, hepatic cysts, radio/trauma/congenital venous
web, renal or adrenal tumours, posterior abd wall sarcoma
Clinical features
Acute: abd pain, tender hepatomegaly, ascites, nausea, vomiting
Chronic: hepatomegaly, splenomegaly dt portal hpt, mild
jaundice, ascites, -ve hepatojugular reflux
Ix
1. LFT –high protein
2. Liver histology-centrizonal congestion, haemorrhage,
fibrosis, cirrhosis
3. Imging- uss, ct, mri – hapatic venous occlusion, abN
parenchyma
4. Doppler sonography
5. Thrombophilia screening (mandatory)
DD
1. Inf vena cava occlusion
2. R cardiac failure
3. Non constrictive pericarditis

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MED Ascites

  • 2.
  • 3. Hepatomegaly • Liver – Malignancy – hepatoma/ metastases – Infection – Hepatitis, abscess, typhoid – Alcohol – fatty liver • Non liver causes – Congestive heart failure – Hemolytic anaemia, myeloproliferative disorder (leukemia) – Autoimmune • Others – Wilson disease (rare)
  • 4. Splenomegaly • C ongestion- congestive heart failure, portal hpt • H emolytic anemia – Thal, heriditary spherocytosis • I nfection – Bacteria : IE, typhoid – Viral : IM, CMV – Parasite : malaria – Fungal • N eoplasm – myeloproliferative/ lymphoproliferative • A utoimmune - CTD
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  • 6. ascites Classified by serum ascites to albumin concentration gradient High gradient (>11g/L) 1.Cirrhosis 2.Budd chiari syndrome 3. Alholic hepatitis 4. Fulminant hepatic failure 5. Congestive heart failure, contrictive pericarditis (cardiac ascites) 6. Myxedema Low gradient (<11gL) 1. Peritoneal ascites 2. Tb 3. Pancreatic ascites 4. Nephrotic syndrome
  • 7. *serum-ascitic albumin gradient (SAAG) = serum albumin value- ascitic fluid albumin value High gradient (TRANSUDATIVE)= incr hydrostatic pressure within blood vessels of hepatic portal system, pushes the fluid into peritoneal cavity, leaving protein such as albumin in the serum Low gradient (EXUDATIVE)= not associated with portal pressure
  • 8. • Transudate – dt incr hydrostatic pressure, red oncotic pressure, Na+ retention. Low protein • Exudate – incr permeability of vessels, lymphatic obstruction. Rich in protein
  • 9. cirrhosis Definition -Necrosis of liver cell>nodule formation& fibrosis -Abnormal liver architecture & liver blood flow and function -Produce clinical features of portal hpt and impaired liver cell fx Causes #Common- hep(c or b+/-d), alcohol or non alcoholic fatty liver ds #others: biliary cirrhosis, autoimmune hep, budd chiari, {heriditary haemochromatosis, wilson) Pathogenesis Activation of stellate cells>proliferation of fibroblast>deposition of collagen Pathology -Characteristic features: regenerating nodules sep by fibrous septa. Loss of N architecture within nodules. -2 types: micro & macronodular cirrhosis Micro Macro Ongoing alcohol damage chr viral hep Biliary tract ds
  • 10. Symptoms -R hypochondriac pain -abd distension -ankle swelling -hematemesis and malena (varices dt portal hpt causing GI bleed) -pruritus (skin-cholestasis dt primary biliary cirrhosis) -gynaecomastia, loss of libido, amenorrhea (endocrine dysfunction) -confusion and drowsiness (neuropsychiatric manifestation dt portosystemic encephalopathy)
  • 11. Signs Periphery -dupuytren contracture (alcoholic cirrhosis) -clubbing -palmar erythema (hyperdynamic circ also seen in pregnancy, thyrotoxicosis, RA) -xanthoma(cholesterol deposits in palmar crease or above eyes dt primary biliary cirrhosis) Face, Neck, chest -xanthelasma -parotid gland enlarge -spider naevi (>5 diagnostic, svc distribution, telengiectasia consist of central arteriole and radiating small vessels) -gynaecomastia Abdomen -Hepatomegaly>shrink in established cirrhosis -Splenomeglay(portal hpt) Endocrine Gynaecomastia Testicular atrophy
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  • 13. Ix 1. Severity-LFT(low serum albumin, prolong PT, incr ALP and ALT, if decompesated CLF all will deranged), BUSE (low sodium, high cr >130 worse prognosis) 2. Types: viral serology, autoAb, ig, iron& ferritin, copper&ceruloplasmin, alpha1 antitrypsin 3. Imaging – Abd USS, CT(arterial-hcc, portal- metastases, av- haemangioma), endoscopy (varices/portal hypertensive gastropathy), MRI 4. Liver biopsy
  • 14. Budd-chiari syndrome Definition Obestruction of venous outflow of liver Dt occlusion of haptic veins Causes -1/3 unknown -hypercoagulability state (polycythaemia vera, paroxysmal nocturnal haemoglobinuria) -thrombophilia -ocp -leukemia -others: HCC, hepatic cysts, radio/trauma/congenital venous web, renal or adrenal tumours, posterior abd wall sarcoma
  • 15. Clinical features Acute: abd pain, tender hepatomegaly, ascites, nausea, vomiting Chronic: hepatomegaly, splenomegaly dt portal hpt, mild jaundice, ascites, -ve hepatojugular reflux Ix 1. LFT –high protein 2. Liver histology-centrizonal congestion, haemorrhage, fibrosis, cirrhosis 3. Imging- uss, ct, mri – hapatic venous occlusion, abN parenchyma 4. Doppler sonography 5. Thrombophilia screening (mandatory) DD 1. Inf vena cava occlusion 2. R cardiac failure 3. Non constrictive pericarditis