Kidney Transplantation in Systemic Amyloidosis

被引:8
作者
Angel-Korman, Avital [1 ,2 ]
Havasi, Andrea [1 ,2 ]
机构
[1] Boston Univ, Sch Med, Dept Med, Renal Sect, Boston, MA 02118 USA
[2] Boston Univ, Sch Med, Amyloidosis Ctr, Boston, MA 02118 USA
关键词
STEM-CELL TRANSPLANTATION; LIGHT-CHAIN AMYLOIDOSIS; HIGH-DOSE MELPHALAN; MINIMAL RESIDUAL DISEASE; SOLID-ORGAN TRANSPLANTATION; STAGE RENAL-DISEASE; A-I AMYLOIDOSIS; LIVER-TRANSPLANTATION; TRANSTHYRETIN AMYLOIDOSIS; HEREDITARY FIBRINOGEN;
D O I
10.1097/TP.0000000000003170
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The present review discusses current developments and outcomes of renal transplantation in systemic amyloidosis. Amyloidosis can wreak havoc on the architecture and functioning of the kidneys, leading to end-stage renal disease. In recent years, the available treatments, especially for light-chain amyloidosis but also for several of the underlying inflammatory diseases that cause amyloid A amyloidosis have expanded leading to prolonged survival albeit frequently with renal failure. At the same time, there are also increasing numbers of patients diagnosed with one of the inherited forms of amyloidosis for which currently there is no targeted treatment available and, in some cases, renal failure is unavoidable. Due to the complex nature of the pathophysiology and treatment of these diseases, it can be very challenging for the clinician to determine whether or not it is appropriate to refer an affected individual for kidney transplantation. Determining eligibility criteria, as well as peritransplant and posttransplant management, requires a multidisciplinary approach with close monitoring and follow-up.
引用
收藏
页码:2035 / 2047
页数:13
相关论文
共 132 条
[21]   Liver Transplantation for Hereditary Transthyretin Amyloidosis: After 20 Years Still the Best Therapeutic Alternative? [J].
Ericzon, Bo-Goran ;
Wilczek, Henryk E. ;
Larsson, Marie ;
Wijayatunga, Priyantha ;
Stangou, Arie ;
Pena, Joao Rodrigues ;
Furtado, Emanuel ;
Barroso, Eduardo ;
Daniel, Jorge ;
Samuel, Didier ;
Adam, Rene ;
Karam, Vincent ;
Poterucha, John ;
Lewis, David ;
Ferraz-Neto, Ben-Hur ;
Cruz, Marcia Waddington ;
Munar-Ques, Miguel ;
Fabregat, Juan ;
Ikeda, Shu-ichi ;
Ando, Yukio ;
Heaton, Nigel ;
Otto, Gerd ;
Suhr, Ole .
TRANSPLANTATION, 2015, 99 (09) :1847-1854
[22]   Liver transplant alone without kidney transplant for fibrinogen A-chain (AFib) renal amyloidosis [J].
Fix, Oren K. ;
Stock, Peter G. ;
Lee, Brian K. ;
Benson, Merrill D. .
AMYLOID-JOURNAL OF PROTEIN FOLDING DISORDERS, 2016, 23 (02) :132-133
[23]   Next Generation Flow for highly sensitive and standardized detection of minimal residual disease in multiple myeloma [J].
Flores-Montero, J. ;
Sanoja-Flores, L. ;
Paiva, B. ;
Puig, N. ;
Garcia-Sanchez, O. ;
Boettcher, S. ;
van der Velden, V. H. J. ;
Perez-Moran, J-J ;
Vidriales, M-B ;
Garcia-Sanz, R. ;
Jimenez, C. ;
Gonzalez, M. ;
Martinez-Lopez, J. ;
Corral-Mateos, A. ;
Grigore, G-E ;
Fluxa, R. ;
Pontes, R. ;
Caetano, J. ;
Sedek, L. ;
del Canizo, M-C ;
Blade, J. ;
Lahuerta, J-J ;
Aguilar, C. ;
Barez, A. ;
Garcia-Mateo, A. ;
Labrador, J. ;
Leoz, P. ;
Aguilera-Sanz, C. ;
San-Miguel, J. ;
Mateos, M-V ;
Durie, B. ;
van Dongen, J. J. M. ;
Orfao, A. .
LEUKEMIA, 2017, 31 (10) :2094-2103
[24]   DIALYSIS SUPPORT OF PATIENTS WITH PRIMARY SYSTEMIC AMYLOIDOSIS - A STUDY OF 211 PATIENTS [J].
GERTZ, MA ;
KYLE, RA ;
OFALLON, WM .
ARCHIVES OF INTERNAL MEDICINE, 1992, 152 (11) :2245-2250
[25]   Immunoglobulin light chain amyloidosis and the kidney [J].
Gertz, MA ;
Lacy, MQ ;
Dispenzieri, A .
KIDNEY INTERNATIONAL, 2002, 61 (01) :1-9
[26]   Clinical outcome of immunoglobulin light chain amyloidosis affecting the kidney [J].
Gertz, Morie A. ;
Leung, Nelson ;
Lacy, Martha Q. ;
Dispenzieri, Angela ;
Zeldenrust, Steven R. ;
Hayman, Suzanne R. ;
Buadi, Francis K. ;
Dingli, David ;
Greipp, Philip R. ;
Kumar, Shaji K. ;
Lust, John A. ;
Rajkumar, S. Vincent ;
Russell, Stephen J. ;
Witzig, Thomas E. .
NEPHROLOGY DIALYSIS TRANSPLANTATION, 2009, 24 (10) :3132-3137
[27]   Organ transplantation in hereditary apolipoprotein Al amyloidosis [J].
Gillmore, J. D. ;
Stangou, A. J. ;
Lachmann, H. J. ;
Goodman, H. J. ;
Wechalekar, A. D. ;
Acheson, J. ;
Tennent, G. A. ;
Bybee, A. ;
Gilbertson, J. ;
Rowczenio, D. ;
O'Grady, J. ;
Heaton, N. D. ;
Pepys, M. B. ;
Hawkins, P. N. .
AMERICAN JOURNAL OF TRANSPLANTATION, 2006, 6 (10) :2342-2347
[28]   Clinical and biochemical outcome of hepatorenal transplantation for hereditary systemic amyloidosis associated with apolipoprotein AI Gly26Arg [J].
Gillmore, JD ;
Stangou, AJ ;
Tennent, GA ;
Booth, DR ;
O'Grady, J ;
Rela, M ;
Heaton, ND ;
Wall, CA ;
Keogh, JAB ;
Hawkins, PN .
TRANSPLANTATION, 2001, 71 (07) :986-992
[29]   Hereditary fibrinogen A α-chain amyloidosis: clinical phenotype and role of liver transplantation [J].
Gillmore, Julian D. ;
Lachmann, Helen J. ;
Wechalekar, Ashutosh ;
Hawkins, Philip N. .
BLOOD, 2010, 115 (21) :4313-4313
[30]   Diagnosis, Pathogenesis, Treatment, and Prognosis of Hereditary Fibrinogen Aα-Chain Amyloidosis [J].
Gillmore, Julian D. ;
Lachmann, Helen J. ;
Rowczenio, Dorota ;
Gilbertson, Janet A. ;
Zeng, Cai-Hong ;
Liu, Zhi-Hong ;
Li, Lei-Shi ;
Wechalekar, Ashutosh ;
Hawkins, Philip N. .
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2009, 20 (02) :444-451