ICD-11 code : DB96.1;

Preferred Label : Primary biliary cholangitis;

ICD-11 definition : Primary biliary cholangitis is characterized by progressive destruction and disappearance of the intralobularbile duct epithelial cells leading to cholestasis (high alkaline phosphatase and GGT {gamma glutamyl transferase}) and eventually liver cirrhosis and liver failure, generally associated with the presence of circulating antimitochondrial antibodies and an increase of serum IgM levels.;

ICD-11 synonym : Tannhauser-Magendantz syndrome; Mahon-Tannhauser syndrome; Hanot-Rossle syndrome; Todd cirrhosis; monolobular cirrhosis; xanthomatous biliary cirrhosis.; Hanot syndrome; toxic cirrhosis; Charcot cirrhosis; pericholangiolic biliary cirrhosis; chronic nonsuppurative destructive cholangitis; primary biliary cirrhosis; Hanot cirrhosis; hypertrophic cirrhosis; hypertrophic biliary cirrhosis;

ICD-11 inclusion : unilobar cirrhosis; chronic nonsuppurative destructive cholangitis;

ICD-11 "other" category code : DB96.1Y;

ICD-11 "unspecified" category code : DB96.1Z;

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Primary biliary cholangitis is characterized by progressive destruction and disappearance of the intralobularbile duct epithelial cells leading to cholestasis (high alkaline phosphatase and GGT {gamma glutamyl transferase}) and eventually liver cirrhosis and liver failure, generally associated with the presence of circulating antimitochondrial antibodies and an increase of serum IgM levels.

https://www.filfoie.com/wp-content/uploads/2019/08/Guidelines-EASL-CBP-version-patient-VF.pdf
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disease management
patient education handout
cholangitis

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18/05/2024


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