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Volume 37 Issue 9
Sep.  2021
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Article Navigation >  Journal of Clinical Hepatology  > 2021  >  37(9): 2188-2190

Living-related donor liver transplantation for pediatric patients with Caroli disease: A case report

DOI: 10.3969/j.issn.1001-5256.2021.09.037
  • 1.

    School of Clinical Medicine, Guizhou Medical University, Guiyang 550004, China

  • 2a.

    Department of Transplantation, The Affiliated Hospital of Guizhou Medical University, Guiyang 550004, China

  • 2b.

    Department of Hepatobiliary Surgery, The Affiliated Hospital of Guizhou Medical University, Guiyang 550004, China

Research funding:

Science and Technology Fund of Guizhou Province (QKHJC 〔2019〕 No. 1267)

  • Received Date: 2021-01-14
  • Accepted Date: 2021-02-10
  • Published Date: 2021-09-20
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    • References(22)
  • [1]
    HAN X, DING XL, LI XM, et al. Gastrointestinal bleeding induced by Caroli disease: A case report[J]. J Clin Hepatol, 2020, 36(1): 169-170. DOI: 10.3969/j.issn.1001-5256.2020.01.039.

    韩西, 丁晓玲, 李雪梅, 等. Caroli病引发上消化道出血1例报告[J]. 临床肝胆病杂志, 2020, 36(1): 169-170. DOI: 10.3969/j.issn.1001-5256.2020.01.039.
    [2]
    WEHRMAN A, KRIEGERMEIER A, WEN J. Diagnosis and management of hepatobiliary complications in autosomal recessive polycystic kidney disease[J]. Front Pediatr, 2017, 5: 124. DOI: 10.3389/fped.2017.00124.
    [3]
    MAVLIKEEV M, TITOVA A, SAITBURKHANOVA R, et al. Caroli syndrome: A clinical case with detailed histopathological analysis[J]. Clin J Gastroenterol, 2019, 12(2): 106-111. DOI: 10.1007/s12328-018-0917-6.
    [4]
    LI J, LIU LW, LUO J, et al. Clinicopathological features of Caroli disease/Caroli syndrome: An analysis of 21 cases[J]. Natl Med J China, 2020, 100(38): 3005-3009. DOI: 10.3760/cma.j.cn112137-20200630-01995.

    李娟, 刘立伟, 罗娟, 等. Caroli病或Caroli综合征患者21例临床病理特征分析[J]. 中华医学杂志, 2020, 100(38): 3005-3009. DOI: 10.3760/cma.j.cn112137-20200630-01995.
    [5]
    KUMAR A, AKSELROD D, PRIKIS M. Caroli disease revisited: A case of a kidney transplant patient with autosomal polycystic kidney disease and recurrent episodes of cholangitis[J]. Transplant Proc, 2019, 51(2): 541-544. DOI: 10.1016/j.transproceed.2018.12.025.
    [6]
    FAHRNER R, DENNLER SG, INDERBITZIN D. Risk of malignancy in Caroli disease and syndrome: A systematic review[J]. World J Gastroenterol, 2020, 26(31): 4718-4728. DOI: 10.3748/wjg.v26.i31.4718.
    [7]
    Section of Biliary Surgery, Branch of Surgery, Chinese Medical Association. Guideline for the diagnosis and treatment for biliary dilatation (2017 edition)[J]. Chin J Dig Surg, 2017, 16(8): 767-774. DOI: 10.3760/cma.j.issn.1673-9752.2017.08.001.

    中华医学会外科学分会胆道外科学组. 胆管扩张症诊断与治疗指南(2017版)[J]. 中华消化外科杂志, 2017, 16(8): 767-774. DOI: 10.3760/cma.j.issn.1673-9752.2017.08.001.
    [8]
    SHI W, HUANG XM, FENG YL, et al. Factors contributing to diagnostic delay of Caroli syndrome: A single-center, retrospective study[J]. BMC Gastroenterol, 2020, 20(1): 317. DOI: 10.1186/s12876-020-01442-5.
    [9]
    MOSLIM MA, GUNASEKARAN G, VOGT D, et al. Surgical management of Caroli's disease: Single center experience and review of the literature[J]. J Gastrointest Surg, 2015, 19(11): 2019-2027. DOI: 10.1007/s11605-015-2918-9.
    [10]
    FAHRNER R, DENNLER S, DONDORF F, et al. Liver resection and transplantation in Caroli disease and syndrome[J]. J Visc Surg, 2019, 156(2): 91-95. DOI: 10.1016/j.jviscsurg.2018.06.001.
    [11]
    ROMINE MM, WHITE J. Role of transplant in biliary disease[J]. Surg Clin North Am, 2019, 99(2): 387-401. DOI: 10.1016/j.suc.2018.12.009.
    [12]
    HARRING TR, NGUYEN NT, LIU H, et al. Caroli disease patients have excellent survival after liver transplant[J]. J Surg Res, 2012, 177(2): 365-372. DOI: 10.1016/j.jss.2012.04.022.
    [13]
    MILLWALA F, SEGEV DL, THULUVATH PJ. Caroli's disease and outcomes after liver transplantation[J]. Liver Transpl, 2008, 14(1): 11-17. DOI: 10.1002/lt.21366.
    [14]
    TENG DH, WU D, ZHANG W, et al. Liver transplantation in the treatment of Caroli syndrome: A single- center experience[J]. Chin J Surg, 2020, 58(12): 956-958. DOI: 10.3760/cma.j.cn112139-20200507-00364.

    滕大洪, 吴迪, 张威, 等. 肝移植治疗Caroli综合征单中心经验[J]. 中华外科杂志, 2020, 58(12): 956-958. DOI: 10.3760/cma.j.cn112139-20200507-00364.
    [15]
    KHAN K, SCHWARZENBERG SJ, SHARP HL, et al. Morbidity from congenital hepatic fibrosis after renal transplantation for autosomal recessive polycystic kidney disease[J]. Am J Transplant, 2002, 2(4): 360-365. DOI: 10.1034/j.1600-6143.2002.20412.x.
    [16]
    CHAPAL M, DEBOUT A, DUFAY A, et al. Kidney and liver transplantation in patients with autosomal recessive polycystic kidney disease: A multicentric study[J]. Nephrol Dial Transplant, 2012, 27(5): 2083-2088. DOI: 10.1093/ndt/gfr588.
    [17]
    Chinese Society of Organ Transplantation, Chinese Medical Association. Technical specification for pediatric liver transplantation in China (2019 edition)[J/CD]. Chin J Transplant (Electronic Edition), 2019, 13(3): 181-186. DOI: 10.3877/cma.j.issn.1674-3903.2019.03.005.

    中华医学会器官移植学分会. 中国儿童肝移植操作规范(2019版)[J/CD]. 中华移植杂志(电子版), 2019, 13(3): 181-186. DOI: 10.3877/cma.j.issn.1674-3903.2019.03.005.
    [18]
    LYU GY. Advancement and prospect of living donor liver transplantation (2000-2020)[J]. Chin J Pract Surg, 2020, 40(2): 163-166, 170. DOI: 10.19538/j.cjps.issn1005-2208.2020.02.06.

    吕国悦. 活体肝移植进展与展望(2000-2020)[J]. 中国实用外科杂志, 2020, 40(2): 163-166, 170. DOI: 10.19538/j.cjps.issn1005-2208.2020.02.06.
    [19]
    YU HL, YU WL, WENG YQ, et al. Changes in levels of brain injury markers in serum during perioperative period in infants underwent parent liver transplantation and their clinical significances[J]. J Jilin Univ (Med Edit), 2021, 47(1): 168-172. DOI: 10.13481/j.1671-587X.20210123.

    于洪丽, 喻文立, 翁亦齐, 等. 亲体肝移植患儿围术期血清中脑损伤标志物水平的变化及临床意义[J]. 吉林大学学报(医学版), 2021, 47(1): 168-172. DOI: 10.13481/j.1671-587X.20210123.
    [20]
    GU GX, ZONG ZP, ZHOU T, et al. Living related donor liver transplantation for infant with Crigler-Najjar syndrome type Ⅰ: A report of one case and literature review[J]. Ogran Transplantation, 2020, 11(4): 471-476. DOI: 10.3969/j.issn.1674-7445.2020.04.008.

    顾广祥, 宗志鹏, 周韬, 等. 亲属活体肝移植治疗婴儿Crigler-Najjar综合征Ⅰ型1例并文献复习[J]. 器官移植, 2020, 11(4): 471-476. DOI: 10.3969/j.issn.1674-7445.2020.04.008.
    [21]
    LAI Q, LERUT J. Proposal for an algorithm for liver transplantation in Caroli's disease and syndrome: Putting an uncommon effort into a common task[J]. Clin Transplant, 2016, 30(1): 3-9. DOI: 10.1111/ctr.12640.
    [22]
    GAO W, WANG K, MA N, et al. Living donor liver transplantations for pediatric patients withbiliary atresia in a single center: 306 cases report[J]. Chin J Organ Transplant, 2019, 40(1): 13-17. DOI: 10.3760/cma.j.issn.0254-1785.2019.01.004.

    高伟, 王凯, 马楠, 等. 亲属活体肝移植治疗儿童胆道闭锁306例临床分析[J]. 中华器官移植杂志, 2019, 40(1): 13-17. DOI: 10.3760/cma.j.issn.0254-1785.2019.01.004.
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