44-jährige Patientin mit unklarer Leberwerterhöhung und familiär gehäuftem Gallensteinleiden

C. Hopf; U. Beuers; H. Bikker; G. U. Denk; C. Rust

doi:10.1007/s00108-010-2775-2

44-jährige Patientin mit unklarer Leberwerterhöhung und familiär gehäuftem Gallensteinleiden

C. Hopf
, U. Beuers
, H. Bikker
, G. U. Denk
, C. Rust

Research output: Contribution to journal › Article › Academic › peer-review

Abstract

"Low phospholipid associated cholelithiasis" (LPAC) syndrome is an important differential diagnosis in younger patients with biliary symptoms after cholecystectomy and concomitant elevated serum liver tests. Typical symptoms include recurrence of biliary colics after cholecystectomy, echogenic material in the intrahepatic bile ducts, intrahepatic cholestasis of pregnancy or cholestasis under hormonal contraception and a family history of gallstone disease. Patients with LPAC syndrome can be successfully treated with ursodeoxycholic acid

Original language	English
Pages (from-to)	1234-1237
Journal	Internist
Volume	52
Issue number	10
DOIs	https://doi.org/10.1007/s00108-010-2775-2
Publication status	Published - 2011

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

SDG 3 Good Health and Well-being

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10.1007/s00108-010-2775-2

Cite this

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title = "44-j{\"a}hrige Patientin mit unklarer Leberwerterh{\"o}hung und famili{\"a}r geh{\"a}uftem Gallensteinleiden",

abstract = "{"}Low phospholipid associated cholelithiasis{"} (LPAC) syndrome is an important differential diagnosis in younger patients with biliary symptoms after cholecystectomy and concomitant elevated serum liver tests. Typical symptoms include recurrence of biliary colics after cholecystectomy, echogenic material in the intrahepatic bile ducts, intrahepatic cholestasis of pregnancy or cholestasis under hormonal contraception and a family history of gallstone disease. Patients with LPAC syndrome can be successfully treated with ursodeoxycholic acid",

author = "C. Hopf and U. Beuers and H. Bikker and Denk, \{G. U.\} and C. Rust",

year = "2011",

doi = "10.1007/s00108-010-2775-2",

language = "English",

volume = "52",

pages = "1234--1237",

journal = "Internist",

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publisher = "Springer Verlag",

number = "10",

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T1 - 44-jährige Patientin mit unklarer Leberwerterhöhung und familiär gehäuftem Gallensteinleiden

AU - Hopf, C.

AU - Beuers, U.

AU - Bikker, H.

AU - Denk, G. U.

AU - Rust, C.

PY - 2011

Y1 - 2011

N2 - "Low phospholipid associated cholelithiasis" (LPAC) syndrome is an important differential diagnosis in younger patients with biliary symptoms after cholecystectomy and concomitant elevated serum liver tests. Typical symptoms include recurrence of biliary colics after cholecystectomy, echogenic material in the intrahepatic bile ducts, intrahepatic cholestasis of pregnancy or cholestasis under hormonal contraception and a family history of gallstone disease. Patients with LPAC syndrome can be successfully treated with ursodeoxycholic acid

AB - "Low phospholipid associated cholelithiasis" (LPAC) syndrome is an important differential diagnosis in younger patients with biliary symptoms after cholecystectomy and concomitant elevated serum liver tests. Typical symptoms include recurrence of biliary colics after cholecystectomy, echogenic material in the intrahepatic bile ducts, intrahepatic cholestasis of pregnancy or cholestasis under hormonal contraception and a family history of gallstone disease. Patients with LPAC syndrome can be successfully treated with ursodeoxycholic acid

U2 - 10.1007/s00108-010-2775-2

DO - 10.1007/s00108-010-2775-2

M3 - Article

C2 - 21161147

SN - 0020-9554

VL - 52

SP - 1234

EP - 1237

JO - Internist

JF - Internist

IS - 10

ER -

44-jährige Patientin mit unklarer Leberwerterhöhung und familiär gehäuftem Gallensteinleiden

Abstract

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