Abdominal Flashcards

1
Q

Differentiating Caput Medusae from IVC obstruction

A

Compress below umbilicus

● Caput medusa: towards legs
● IVC obstruction: towards heart

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2
Q

Causes of hepatomegaly

A
  1. Massive
    a. Metastases
    b. Alcoholic liver disease with fatty infiltration
    c. Myeloproliferative disease
    d. Right heart failure
    e. Hepatocellular cancer/secondary metastasis
  2. Moderate
    a. Haemochromatosis
    b. Haematological disease – chronic leukaemia, lymphoma,
    c. Fatty liver – secondary to diabetes mellitus, obesity, toxins
    d. Infiltration – e.g. amyloid
  3. Mild
    a. Hepatitis
    b. Biliary obstruction
    c. Hydatid disease
    d. HIV infection

By cause:
Liver - HCC, liver mets, AFLD, NAFLD, haemochromatosis, biliary obstruction, budd chiari.
Cardiac - RHF
Haematological - myloproliferative disease, CML, CLL, lymphoma.
infective - hepatitis, hydatid disease, HIV.
infiltrative - amyloid, gauchers

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3
Q

Causes of a firm and irregular liver

A

● Hepatocellular carcinoma
● Metastatic disease
● Cirrhosis
● Hydatid disease, granuloma (e.g. sarcoid), amyloid, cysts

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4
Q

Causes of a tender liver

A
●	Hepatitis 
●	Rapid liver enlargement – e.g. right heart failure, Budd-Chiari syndrome (hepatic vein thrombosis)
●	Hepatocellular carcinoma 
●	Hepatic abscess 
●	Biliary obstruction/cholangitis
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5
Q

Causes of a pulsatile liver

A

● Tricuspid regurgitation
● Hepatocellular cancer
● Vascular abnormalities

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6
Q

Causes of Hepatosplenomegaly.

A
  1. Chronic liver disease with portal hypertension
  2. Haematological: e.g. myeloproliferative disease, lymphoma, leukaemia, thalassaemia, sickle cell anaemia
  3. Infection, e.g. acute viral hepatitis, EBV, CMV
  4. Infiltration, e.g. amyloid, sarcoid
  5. Connective tissue disease, e.g. systemic lupus erythematosus
  6. Acromegaly
  7. Thyrotoxicosis
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7
Q

Causes of high SAAG (>11g/L)

A
High gradient (>11g/L)
●	Cirrhosis with portal hypertension
●	Alcoholic hepatitis
●	Budd-Chiari syndrome
●	Fulminant hepatic failure
●	Congestive heart failure, constrictive pericarditis 
●	Myxoedema
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8
Q

Causes of Low SAAG (<11g/L)

A
Low gradient (<11g/L)
●	Peritoneal carcinomatosis 
●	Tuberculosis 
●	Pancreatic ascites 
●	Nephrotic syndrome
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9
Q

Signs of liver disease

A

● Hands: leukonychia, clubbing, palmar erythema, bruising, asterixis
● Face: jaundice, scratch marks, spider naevi, fetor hepaticus
● Chest: gynaecomastia, loss of body hair, spider naevi, bruising, pectoral muscle wasting
● Abdomen: hepatosplenomegaly, ascites, signs of portal hypertension, testicular atrophy
● Legs: oedema, muscle wasting, bruising

Signs of decompensation
Synthetic - bile production, albumin production, clotting factor production.
Metatabolic - Macronutrient metabolism, bilirubin metabolism, drug and toxin metabolism (ammonia)

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10
Q

Signs of portal hypertension

A

● Splenomegaly
● Collateral veins
● Ascites

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11
Q

Causes of portal hypertension

A
  1. Cirrhosis of the liver
  2. Other causes
    a. Pre-sinusoidal: portal vein compression, intravascular clotting, umbilical vein phlebitis
    b. Intrahepatic: sarcoid, lymphoma or leukaemic infiltrates, congenital hepatic fibrosis
    c. Post-sinusoidal: hepatic vein outflow obstruction (Budd-Chiari syndrome), veno-occlusive disease, constrictive pericarditis, chronic cardiac failure
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12
Q

Causes of Splenomegaly

A
  1. Infections: EBV, CMV, HIV, Malaria, Endocarditis
  2. Haematological: haemolytic anaemia, Polycythaemia vera, essential thrombocytosis, myelofibrosis, CML, CLL, lymphoma. thalassemia, sickle cell anaemia.
  3. Liver/Vascular: cirrhosis/portal hypertension, splenic vein thrombosis, Budd-Chiari syndrome
  4. Rheumatological: SLE, RA (Felty’s syndrome), Amyloidosis, Sarcoidosis
  5. Other - Gauchers disease
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13
Q

Causes of pancytopenia

A

● Aplastic anaemia: severe hypoplasia of the erythroid, myeloid and platelet precursor cell lines in the bone marrow resulting in a bone marrow that is fatty and empty of cells
● Marrow infiltration by leukaemia, lymphoma, carcinoma myeloma, myelofibrosis or granulomata
● Other: acute leukaemia, pernicious anaemia, hypersplenism, SLE, folate deficiency, PNH

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14
Q

Causes of anaemia

A

Microcytic anaemia
● Iron-deficiency anaemia
● Thalassaemia minor
● Sideroblastic anaemia
● Long-standing anaemia
Macrocytic anaemia
● Megaloblastic bone marrow due to Vitamin B12 deficiency or folate deficiency
● Alcohol
● Cirrhosis of the liver
● Reticulocytosis, e.g. haemolysis, haemorrhage
● Hypothyroidism
● Myelodysplastic syndrome
● Myeloproliferative disease
Normocytic anaemia
● Bone marrow failure
o Aplastic anaemia: drugs, radiation, SLE, viral hepatitis, pregnancy, Fanconi syndrome, idiopathic
o Ineffective haematopoiesis: myelodysplastic syndrome, paroxysmal nocturnal haemoglobinuria
o Infiltration: e.g. leukaemia, lymphoma, myeloma, granuloma, myelofibrosis
● Anaemia of chronic disease
o Chronic inflammation
o Malignancy
o Endocrine deficiencies, e.g. hypothyroidism, hypopituitarism, Addison’s disease
o Liver disease
o Chronic kidney disease
o Malnutrition
● Haemolytic anaemia
o Intracorpuscular defects: e.g. hereditary spherocytoiss, haemoglobinopathies – sickle cell, thalassaemia
o Extracorpuscular defects: e.g. AIHA, truma, MAHA, toxic (malaria)

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15
Q

Causes of polycythemia

A
●	Idiopathic: polycythaemia rubra vera
●	Secondary polycythaemia 
o	Increased erythropoietin:
▪	Renal disease: polycystic disease, hydronephrosis, tumour, after renal transplantation
▪	Hepatocellular carcinoma
▪	Cushing’s syndrome 
o	Hypoxic states
▪	Chronic lung disease 
▪	Sleep apnoea
▪	Living at high altitude 
▪	Cyanotic congenital heart disease
▪	Abnormal haemoglobins
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16
Q

Signs of polycythemia

A

● Plethoric appearance
● Scratch marks (generalised pruritus)
● Splenomegaly
● Bleeding tendency (platelet dysfunction)
● Peripheral vascular and ischaemic heart disease
● Gout
● Mild hypertension

17
Q

Causes of liver cirrhosis

A
Causes- 
Alcohol
- Postviral (hep B/C)
- Non alcoholic steatohepatitis (NASH)
- Drugs (e.g. methyldopa, chlorpromazine, isoniazid, nitrofurantoin, propylthiouracil, methotrexate, amiodarone)
- Autoimmune hepatitis
- Haemochromatosis
- Wilson's disease
- Primary sclerosing cholangitis (PSC)
- Primary biliary cirrhosis (PBC)
- Secondary biliary cirrhosis
- Alpha1 antitrypsin deficiency
- Cystic Fibrosis
- Budd-Chiari Syndrome
- Cardiac Failure, chronic constrictive pericarditis
- Cryptogenic (idiopathic).
18
Q

Signs of Hemochromatosis

A
  • bronzed skin
  • arthropathy (especially 2/3 MCPs)
  • testicular atrophy (hypogonadotrophic hypogonadism) - dilated cardiomyopathy
  • glycosuria (diabetes)
19
Q

Causes of renal masses

A
  • PCKD
  • hydronephrosis
  • hypernephroma (bilat RCC)
  • acute renal vein thrombosis
  • infiltrative: amyloid, lymphoma, sarcoid
  • acromegaly
20
Q

RIF masses

A
  • appendiceal abscess
  • caecal carcinoma
  • crohn’s
  • ilieocaecal tuberculosis
  • carcinoid tumour -
    hernias
  • pelvic kidney
  • psoas abscess
  • ovarian tumour/cyst
21
Q

LIF masses

A
  • faeces (indentable)
  • carcinoma of sigmoid/descending colon
  • diverticular disease
  • hernias
  • ovarian tumour/cyst
  • psoas abscess
22
Q

Upper abdominal masses

A
  • Lymphadenopathy
  • stomach carcinoma
  • pancreatic pseudocyst/tumour
  • pyloric stenosis
  • transverse colon carcinoma
  • hernias
  • AAA (pulsatile)
23
Q

Causes of lymphadenopathy

A

Haematological (rubbery and firm) - lymphoma - leukaemia (CLL, ALL)
Infections - viral: CMV, HIV, EBV, others - bacterial: TB, brucellosis - protazoal: toxoplasmosis
Malignant (very firm) - metastases – reactive
CTD - RA, SLEInfiltration – sarcoid
Drugs - phenytoin (pseudolymphoma)