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23 Cards in this Set

  • Front
  • Back

Causes of hepatomegaly

Common causes are 3 Cs


Cirrhosis, carcinoma & CCF



Other causes are 3 I's


Infiltrative = amyloid, myeloproliferative, Wilson's, HH


Infection = HBV, HCV


Immune = PBC, PSC, autoimmune hep

Causes of ascites

Ascites can be transudative or exudative


Calculate with SAAG = serum albumin - ascitic albumin.


>11mmol/L difference = transudative


<11mmol/L difference = exudative



Exudative = malignancy, pancreatitis, TB peritonitis


Transudative = CCF, liver failure, nephrotic syndrome, Budd-Chiari syndrome (hepatic vein thrombosis/obstruction)

Features of a liver

Felt in RUQ


Moves on inspiration


Cannot get above it


Can be hard and craggy = malignancy/cirrhosis

Signs of decompensated liver disease

3 A's


Asterixis


Abnormal GCS (encephalopathy)


Ascites

Complications of cirrhosis

Varices


Encephalopathy


SBP

Ix to do in hepatomegaly

Bloods = FBC, U+Es, LFTs, albumin, clotting


Imaging = USS


Other = ascitic tap, Echo



Liver screen


Hepatitis serology


AFP (HCC)


Autoantibodies = AMA (PBC), Anti-smooth muscle (autoimmune hep), immunoglobulins (PSC)


Caeruloplasmin


Ferritin


Alpha-1 antitrypsin


May do liver biopsy for ?HCC and ERCP for ?PSC

Management of ascites

Alcohol abstinence


Salt restriction


Diuretics


Therapeutic drains


Liver transplant

DDx for palmar erythema

Cirrhosis


Thyrotoxicosis


RA


Pregnancy


Polycythaemia

DDx of gynaecomastia

Drugs = spirinolactone, digoxin


Liver cirrhosis


Klinefelter's syndrome


Testicular tumours or orchidectomy


Hyper/hypothyroidism or Addison's disease


Physiological = old age, puberty


Causes of splenomegaly

Classify according to size



Massive (>8cm) = myelofibrosis, CML, Gauchers, malaria, visceral leishmaniasis (protazoal infection which is second biggest parasite killer to malaria worldwide)


Moderate (4-8cm) = myeloproliferative disorders


Tip (<4cm) = myeloproliferative disorders, infection (EBV, IE), congestive (portal HTN) and haemolytic anaemia



Features of a spleen on examination

Mass in LUQ


Moves infero-laterally on palpation


Has a notch


Cannot get above it or ballot it

Indications for a splenectomy

Trauma


Haematological = ITP or hereditary spherocytosis

Work up for a splenectomy

Vaccinate (ideally 2/52 before)


- Pneumococcal


- Haemophillus influenza (HiB)


- Meningococcal


Prophylactic penV


Medic alert bracelet

Kidney examination

Peripheral


Signs of immunosuppresion (Cushingoid, gum hypertrophy after ciclosporin)


Fistula (thrill? bruit?) or tunnelled line


HTN



Abdomen


Nephrectomy scar


Rutherford-Morrison scar + renal transplant


Ballotable kidney



(Hepatomegaly, peritoneal dialysis scars, indwelling catheter)


Mention examining external genitalia (varicocele) and dipsticking urine (microscopic haematuria/proteinuria)

Causes of unilateral enlarged kidney

Autosomal dominant polycystic kidney disease


Renal cell Ca


Simple cysts


Hydronephrosis

Causes of bilaterally enlarged kidneys

Autosomal dominant polycystic kidney disease


Bilateral hydronephrosis


Bilateral renal cell Ca


Amyloid


Tuberous sclerosis (renal angiomyolipomata & cysts)

Tuberous sclerosis features

Adenoma sebaceum = facial angiofibromas


Shagreen patches = area of red-orange plaque on sacrum


Ungual fibromas


Renal angiomyolipomata


Ash leaf macules = areas of depigmented skin


Investigations in renal pts.

Bloods = FBC, U+Es


Urine = dipstick


Imaging = USS +/- biopsy, CT KUB


Genetic studies if ?ADPKD

ADPKD


- Frequency


- Genetics


- Clin features


- Extra-renal involvement


- Dx


- Mx

1:1000 affected


Autosomal dominant pattern of inheritance


Most common congenital cause of renal failure. 5% of all end stage renal failure in UK


Clin features = haematuria, recurrent UTIs, abdo pain w/ cyst rupture & HTN


Extra-renal involvement = berry aneurysms (SAH), liver cysts and mitral valve prolapse


Dx = <30yrs needs 2 cysts in 1 kidney, 30-59yrs needs 2 cysts in 2 kidneys and 60yrs+ needs 4 cysts in both kidneys


Mx involves supportive care, dialysis, nephrectomy and trasnplant


Reasons for nephrectomy = size, recurrent infections, HTN and bleeds

Signs in transplant pt.


- Scars


- Liver pt.


- Renal pt.


- Transplant associated signs

Scars = Rutherford-Morrison (kidney) or rooftop/Merc-Benz (liver)


Liver pt. = indications to cause (IVDU/tattoos, pigmented = HH, other autoimmune disease = PBC, evidence of chronic LD)


Renal pt. = nephrectomy scar, ADPKD, fistulae, peritoneal dialysis scars, tunnelled line/scar, signs of DM or autoimmune



Transplant assoc signs


Signs of steroid or ciclosporin use (gum hypertrophy)


Skin cancer = actinic keratoses, SCC (100x increased risk) or BCC/melanoma (10x increased risk)


Infection = warts & cellulitis

Top 3 indications for renal transplant

Glomerulonephritis


Diabetic nephropathy


ADPKD

Top 3 indications for liver transplant

Cirrhosis


Fulminant liver failure (Hep A, B & paracetamol OD)


HCC

Problems post-transplant

Rejection (acute/chronic)


Infection (CMV, PCP)


Pathology assoc = skin Ca, CV disease, lymphoprolif disorders


Recurrence of original disease


Toxicity of immunosuppression


Psychological