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一名儿童因下腔静脉膜状蹼导致布加综合征,经全身及局部重组组织型纤溶酶原激活剂治疗后痊愈。

Budd-Chiari syndrome in a child due to a membranous web of the inferior vena cava resolved by systemic and local recombinant tissue plasminogen activator treatment.

作者信息

Alioğlu Bülent, Avci Zekai, Aytekin Cüneyt, Mercan Sükrü, Ozçay Figen, Kürekçi Emin, Ozbek Namk

机构信息

Department of Pediatric Hematology, Baskent University Faculty of Medicine, Ankara, Turkey.

出版信息

Blood Coagul Fibrinolysis. 2006 Apr;17(3):209-12. doi: 10.1097/01.mbc.0000220244.12412.0b.

DOI:10.1097/01.mbc.0000220244.12412.0b
PMID:16575259
Abstract

Budd-Chiari syndrome is a heterogeneous group of disorders characterized by hepatic venous outflow obstruction. Although there are no guidelines for treatment of patients with Budd-Chiari syndrome, thrombolytic therapy may be useful in patients with acute Budd-Chiari syndrome. In this report, a boy with Budd-Chiari syndrome due to membranous obstruction of the inferior vena cava treated with systemic and local administration of recombinant tissue plasminogen activator is described. We would like to emphasize the role of systemic and local fibrinolytic treatment in these patients.

摘要

布加综合征是一组以肝静脉流出道梗阻为特征的异质性疾病。尽管目前尚无布加综合征患者的治疗指南,但溶栓治疗可能对急性布加综合征患者有用。在本报告中,描述了一名因下腔静脉膜性梗阻导致布加综合征的男孩,接受了重组组织型纤溶酶原激活剂的全身和局部给药治疗。我们想强调全身和局部纤溶治疗在这些患者中的作用。

相似文献

1
Budd-Chiari syndrome in a child due to a membranous web of the inferior vena cava resolved by systemic and local recombinant tissue plasminogen activator treatment.一名儿童因下腔静脉膜状蹼导致布加综合征,经全身及局部重组组织型纤溶酶原激活剂治疗后痊愈。
Blood Coagul Fibrinolysis. 2006 Apr;17(3):209-12. doi: 10.1097/01.mbc.0000220244.12412.0b.
2
Fibrinolytic therapy with rt-PA in a patient with paroxysmal nocturnal hemoglobinuria and Budd-Chiari syndrome.用重组组织型纤溶酶原激活剂对一名阵发性夜间血红蛋白尿合并布加综合征患者进行溶栓治疗。
Ann Hematol. 2003 May;82(5):299-302. doi: 10.1007/s00277-003-0639-8. Epub 2003 Apr 18.
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CT diagnosis of primary Budd-Chiari syndrome--membranous obstruction of the inferior vena cava.原发性布加综合征的CT诊断——下腔静脉膜性梗阻
Radiat Med. 1986 Jul-Sep;4(3):86-8.
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A single-center retrospective study: Clinical features of different types of Budd-Chiari syndrome in Chinese patients in the Hubei area.一项单中心回顾性研究:湖北地区中国患者不同类型布加综合征的临床特征
Vascular. 2018 Feb;26(1):80-89. doi: 10.1177/1708538117718638. Epub 2017 Jul 25.
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Budd-Chiari syndrome: early intervention with angioplasty and thrombolytic therapy.布加综合征:血管成形术和溶栓治疗的早期干预
Mayo Clin Proc. 1994 Sep;69(9):877-81. doi: 10.1016/s0025-6196(12)61791-1.
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[Budd-Chiari syndrome due to membranous obstruction of the inferior vena cava of congenital origin. Ten-year follow-up after radiologic treatment].[先天性下腔静脉膜性梗阻所致布加综合征。放射治疗后十年随访]
Gastroenterol Clin Biol. 1999 Feb;23(2):259-63.
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Pseudo-Budd-Chiari syndrome: extrinsic deformity of the intrahepatic inferior vena cava mimicking membranous obstruction.假性布加综合征:肝内下腔静脉外在畸形酷似膜性梗阻。
J Clin Gastroenterol. 1989 Feb;11(1):88-91.
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[Budd-Chiari syndrome in children and adolescents: therapeutic radiological intervention].儿童及青少年布加综合征:介入放射治疗
Zhonghua Er Ke Za Zhi. 2013 Aug;51(8):590-4.
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Color Doppler imaging findings in patients with Budd-Chiari syndrome: correlation with venographic findings.布加综合征患者的彩色多普勒成像表现:与静脉造影结果的相关性
AJR Am J Roentgenol. 1993 Aug;161(2):307-12. doi: 10.2214/ajr.161.2.8333368.
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Budd-Chiari syndrome with inferior vena cava obstruction associated with systemic lupus erythematosus.布加综合征合并下腔静脉阻塞伴系统性红斑狼疮
J Clin Gastroenterol. 1984 Jun;6(3):253-6.

引用本文的文献

1
Percutaneous sharp recanalization of a membranous IVC occlusion with an occlusion balloon as a needle target.以闭塞球囊为针靶点对膜性下腔静脉闭塞进行经皮锐性再通。
Radiol Case Rep. 2017 Jun 7;12(3):537-541. doi: 10.1016/j.radcr.2017.04.021. eCollection 2017 Sep.
2
Hydatid cyst of liver complicated with budd-Chiari syndrome and portal vein thrombosis.肝包虫囊肿合并布加综合征及门静脉血栓形成。
N Am J Med Sci. 2013 Mar;5(3):242-4. doi: 10.4103/1947-2714.109206.
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Imaging and interventions in Budd-Chiari syndrome.布加综合征的影像学检查与干预措施
World J Radiol. 2011 Jul 28;3(7):169-77. doi: 10.4329/wjr.v3.i7.169.