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Hepatic involvement in hereditary hemorrhagic telangiectasia: an unusual indication for liver transplantation.

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Hepatic involvement in hereditary hemorrhagic telangiectasia: an unusual indication for liver transplantation. / Hillert, Christian; Broering, D C; Gundlach, M; Knoefel, W T; Izbicki, J R; Rogiers, X.

in: LIVER TRANSPLANT, Jahrgang 7, Nr. 3, 3, 2001, S. 266-268.

Publikationen: SCORING: Beitrag in Fachzeitschrift/Zeitung › SCORING: Zeitschriftenaufsatz › Forschung › Begutachtung

Harvard

Hillert, C, Broering, DC, Gundlach, M, Knoefel, WT, Izbicki, JR & Rogiers, X 2001, 'Hepatic involvement in hereditary hemorrhagic telangiectasia: an unusual indication for liver transplantation.', LIVER TRANSPLANT, Jg. 7, Nr. 3, 3, S. 266-268. <http://www.ncbi.nlm.nih.gov/pubmed/11244170?dopt=Citation>

APA

Hillert, C., Broering, D. C., Gundlach, M., Knoefel, W. T., Izbicki, J. R., & Rogiers, X. (2001). Hepatic involvement in hereditary hemorrhagic telangiectasia: an unusual indication for liver transplantation. LIVER TRANSPLANT, 7(3), 266-268. [3]. http://www.ncbi.nlm.nih.gov/pubmed/11244170?dopt=Citation

Vancouver

Hillert C, Broering DC, Gundlach M, Knoefel WT, Izbicki JR, Rogiers X. Hepatic involvement in hereditary hemorrhagic telangiectasia: an unusual indication for liver transplantation. LIVER TRANSPLANT. 2001;7(3):266-268. 3.

Bibtex

@article{42352f43bac9428ca493a2f8cf22a0dc,
title = "Hepatic involvement in hereditary hemorrhagic telangiectasia: an unusual indication for liver transplantation.",
abstract = "Hereditary hemorrhagic telangiectasia (HHT) is a vascular disease with multiple organ manifestations. Severe hepatic involvement is an unusal indication for liver transplantation. We report on a 39-year-old woman diagnosed with HHT and decompensation of the disease during her second pregnancy. After delivery, hemobilia occurred, followed by severe therapy-resistant cholangitis and progressive liver dysfunction. Because of progressive loss of liver function, orthotopic liver transplantation needed to be performed. The various aspects of liver involvement in Osler's disease, diagnosis, and therapy are discussed.",
author = "Christian Hillert and Broering, {D C} and M Gundlach and Knoefel, {W T} and Izbicki, {J R} and X Rogiers",
year = "2001",
language = "Deutsch",
volume = "7",
pages = "266--268",
journal = "LIVER TRANSPLANT",
issn = "1527-6465",
publisher = "John Wiley and Sons Ltd",
number = "3",

}

RIS

TY - JOUR

T1 - Hepatic involvement in hereditary hemorrhagic telangiectasia: an unusual indication for liver transplantation.

AU - Hillert, Christian

AU - Broering, D C

AU - Gundlach, M

AU - Knoefel, W T

AU - Izbicki, J R

AU - Rogiers, X

PY - 2001

Y1 - 2001

N2 - Hereditary hemorrhagic telangiectasia (HHT) is a vascular disease with multiple organ manifestations. Severe hepatic involvement is an unusal indication for liver transplantation. We report on a 39-year-old woman diagnosed with HHT and decompensation of the disease during her second pregnancy. After delivery, hemobilia occurred, followed by severe therapy-resistant cholangitis and progressive liver dysfunction. Because of progressive loss of liver function, orthotopic liver transplantation needed to be performed. The various aspects of liver involvement in Osler's disease, diagnosis, and therapy are discussed.

AB - Hereditary hemorrhagic telangiectasia (HHT) is a vascular disease with multiple organ manifestations. Severe hepatic involvement is an unusal indication for liver transplantation. We report on a 39-year-old woman diagnosed with HHT and decompensation of the disease during her second pregnancy. After delivery, hemobilia occurred, followed by severe therapy-resistant cholangitis and progressive liver dysfunction. Because of progressive loss of liver function, orthotopic liver transplantation needed to be performed. The various aspects of liver involvement in Osler's disease, diagnosis, and therapy are discussed.

M3 - SCORING: Zeitschriftenaufsatz

VL - 7

SP - 266

EP - 268

JO - LIVER TRANSPLANT

JF - LIVER TRANSPLANT

SN - 1527-6465

IS - 3

M1 - 3

ER -