Transplantation in autosomal recessive polycystic kidney disease: liver and/or kidney?

被引:8
作者
Chandar, Jayanthi [1 ]
Garcia, Jennifer [2 ]
Jorge, Lydia [3 ]
Tekin, Akin [4 ]
机构
[1] Univ Miami, Miller Sch Med, Holtz Childrens Hosp, Div Pediat Nephrol,Dept Pediat, Miami, FL 33101 USA
[2] Univ Miami, Miller Sch Med, Holtz Childrens Hosp, Div Pediat Gastroenterol,Dept Pediat, Miami, FL 33101 USA
[3] Univ Miami, Miller Sch Med, Dept Anesthesiol, Miami, FL 33101 USA
[4] Univ Miami, Miller Sch Med, Div Transplantat, Dept Surg, Miami, FL 33101 USA
关键词
ARPKD; Combined liver kidney transplant; Children; Congenital hepatic fibrosis; CONGENITAL HEPATIC-FIBROSIS; PORTAL-HYPERTENSION; RENAL-TRANSPLANTATION; HEPATOPULMONARY SYNDROME; PRIMARY HYPEROXALURIA; CLINICAL-EXPERIENCE; MACHINE PERFUSION; PKHD1; MUTATIONS; COLD-STORAGE; CHILDREN;
D O I
10.1007/s00467-014-2887-3
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Autosomal recessive polycystic kidney disease (ARPKD) is characterized by enlarged kidneys with dilated collecting ducts and congenital hepatic fibrosis. There is a variable rate of progression of kidney and liver disease. Portal hypertension and Caroli's disease occur from liver involvement that contributes to morbidity and mortality. Approximately 40 % of patients have a severe disease phenotype leading to rapid onset of end-stage kidney disease (ESKD) and signs of portal hypertension and the rest may have predominant involvement of either the kidney or liver. It is important for the physician to establish the extent of organ involvement before deciding on the ultimate plan of management, especially when transplantation is required. Isolated renal transplantation can be considered when liver involvement is minimal. If hepatobiliary disease is prominent, and kidney function is preserved, management options are based on individual characteristics. In the presence of significant liver disease and ESKD, consideration should be given to combined liver kidney transplantation, which can be beneficial in eliminating the consequences of both kidney and liver disease. However, this is a complex surgical procedure that needs to be performed at experienced transplant centers. Improvement in surgical techniques has considerably improved short-term graft survival with the added advantage of the liver offering immunologic protection to the kidney allograft.
引用
收藏
页码:1233 / 1242
页数:10
相关论文
共 63 条
  • [1] Unexplained cyanosis revealing hepatopulmonary syndrome in a child with asymptomatic congenital hepatic fibrosis: A case report
    Wahab A.A.
    Al-Mansoori M.
    El-Hawli M.
    Kini V.
    [J]. Journal of Medical Case Reports, 7 (1)
  • [2] Ananthakrishnan Ashwin N, 2007, Curr Gastroenterol Rep, V9, P151
  • [3] En bloc heterotopic auxiliary liver and bilateral renal transplant in a patient with homozygous protein C deficiency
    Angelis, M
    Pegelow, CH
    Khan, FA
    Verzaro, R
    Tzakis, AG
    [J]. JOURNAL OF PEDIATRICS, 2001, 138 (01) : 120 - 122
  • [4] Cell salvage as part of a blood conservation strategy in anaesthesia
    Ashworth, A.
    Klein, A. A.
    [J]. BRITISH JOURNAL OF ANAESTHESIA, 2010, 105 (04) : 401 - 416
  • [5] Optimizing outcomes for neonatal ARPKD
    Beaunoyer, Mona
    Snehal, Mohile
    Li, Li
    Concepcion, Waldo
    Salvatierra, Oscar, Jr.
    Sarwal, Minnie
    [J]. PEDIATRIC TRANSPLANTATION, 2007, 11 (03) : 267 - 271
  • [6] Transjugular intrahepatic portosystemic shunt prior to renal transplantation in a child with autosomal-recessive polycystic kidney disease and portal hypertension: A case report
    Benador, N
    Grimm, P
    Lavine, J
    Rosenthal, P
    Reznik, V
    Lemire, J
    [J]. PEDIATRIC TRANSPLANTATION, 2001, 5 (03) : 210 - 214
  • [7] PKHD1 mutations in autosomal recessive polycystic kidney disease (ARPKD)
    Bergmann, C
    Senderek, J
    Küpper, F
    Schneider, F
    Dornia, C
    Windelen, E
    Eggermann, T
    Rudnik-Schöneborn, S
    Kirfel, J
    Furu, L
    Onuchic, LE
    Rossetti, S
    Harris, PC
    Somlo, S
    Guay-Woodford, L
    Germino, GG
    Moser, M
    Büttner, R
    Zerres, K
    [J]. HUMAN MUTATION, 2004, 23 (05) : 453 - 463
  • [8] Portosystemic shunts in children: A 15-year experience
    Botha, JF
    Campos, BD
    Grant, WJ
    Horslen, SP
    Sudan, DL
    Shaw, BW
    Langnas, AN
    [J]. JOURNAL OF THE AMERICAN COLLEGE OF SURGEONS, 2004, 199 (02) : 179 - 185
  • [9] Clinical manifestations of autosomal recessive polycystic kidney disease (ARPKD): kidney-related and non-kidney-related phenotypes
    Buescher, Rainer
    Buescher, Anja K.
    Weber, Stefanie
    Mohr, Julia
    Hegen, Bianca
    Vester, Udo
    Hoyer, Peter F.
    [J]. PEDIATRIC NEPHROLOGY, 2014, 29 (10) : 1915 - 1925
  • [10] Indications for combined liver and kidney transplantation in children
    Chava, Srinivas P.
    Singh, Balbir
    Pal, Sujoy
    Dhawan, Anil
    Heaton, Nigel D.
    [J]. PEDIATRIC TRANSPLANTATION, 2009, 13 (06) : 661 - 669