Blood supply презентация

Copyright ©2001 BMJ Publishing Group Ltd. Beckingham, I J et al. BMJ 2001;322:477-480 Couinaud’s segmental anatomy of the liver

Слайд 1- weight: 1-1.5 kg ? largest body organ
- represents 1.5-2.5% lean

body mass
- held in place by ligamentous attachments to diaphragm, peritoneum, great vessels and upper GI organs



Слайд 2Copyright ©2001 BMJ Publishing Group Ltd.
Beckingham, I J et al. BMJ

2001;322:477-480

Couinaud’s segmental anatomy of the liver


Слайд 3
blood supply

- receives dual blood supply:
20% = hepatic artery: oxygen-rich
80%

= portal vein: nutrient rich
cell majority (2/3 of liver mass): hepatocytes
other cell types: Kupffer cells
stellate (Ito or fat-storing) cells bile ductular structures supporting structures

Слайд 4Liver Test Patterns in Hepatobiliary Disorders
Type of disorder Bilirubin Aminotransferases

Hemolysis/Gilbert’s Normal to 5 mg/dl Normal

Syndrome 85% due to indirect
fractions
No bilirubinuria

Acute Hepatocellular Both fractions may Elevated, often
necrosis (viral and be elevated > 500 IU
drug hepatitis , Peak usually follows ALT > AST
hepatotoxins, acute aminotransferase
heart failure) Bilirubinuria

Chronic hepatocellular Both fractions may Elevated, usually
disorders be elevated < 300 IU
Bilirubinuria

Слайд 5
Score Bilirubin Albumin PT (Sec)

Encephal Ascites
(mg/dl) (gm/dl)

1 < 2 > 3.5 1 - 4 None None

2 2 - 3 2.8 - 3.5 4 – 6 1 - 2 Mild

3 > 3 < 2.8 > 6 3 – 4 Severe



Child class:
A: 5 – 6
B: 7 – 9
C: > 9.


Слайд 6Causes of portal hypertension
SINUSOIDAL
SARCOIDOSIS
SCHISTOSOMIASIS
NODULAR REGENERATIVE HYPERPLASIA
CONGENITAL HEPATIC FIBROSIS
IDIOPATHIC PORTAL

FIBROSIS
EARLY PRIMARY BILIARY CIRRHOSIS
CHRONIC ACTIVE HEPATITIS
MYELOPROLIFERATIVE DISORDER
GRAFT VS HOST DISEASE

Слайд 7CIRRHOSIS
Term was 1st coined by Laennec in 1826
Many definitions but common

theme is injury, repair, regeneration and scarring
NOT a localized process; involves entire liver
Primary histologic features:
Marked fibrosis
Destruction of vascular & biliary elements
Regeneration
Nodule formation

Слайд 8Classification of Cirrhosis

WHO divided cirrhosis into 3 categories based on morphological

characteristics of the hepatic nodules
Micronodular
Macronodular
Mixed

Слайд 9DIAGNOSIS
Can be asymptomatic for decades
History
Physical findings: Hepatomegaly, jaundice, ascites, spider

angioma, splenomegaly, palmar erythema, fetor hepaticus, purpura etc.
Elevated LFTs, thrombocytopenia,

Слайд 10Of course the definitive treatment for most of the complications of

end- stage liver disease, including recurrent GI bleeding due to severe portal hypertension,

orthotopic liver transplantation.

Since the presence of a surgical portacaval or mesocaval shunt greatly complicates the transplantation procedure, we have generally abandoned these types of shunting operations in patients with cirrhosis.



Management


Слайд 11SURGERY
1- LIVER TRANSPLANTATION
ONLY DEFINITIVE PROCEDURE

# primary in Child’s C
2- SHUNT PROCEDURE

3- DEVASCULARIZATION

Слайд 12Devascularization
Sugiura procedure
mortality is 10-35%
5% recurrence rate of rebleeding
thoraco & abdominal incision
splenectomy,

devasc. Stomach, esopsophagus, transect the esoph with reanastamosis, ligate all collaterals


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