期刊文献+

原发疾病隐匿的布-加综合征11例临床分析 被引量:1

Clinical analysis of 11 Budd-Chiari syndrome cases which occurred from occult primary disease
下载PDF
导出
摘要 目的分析继发于其他疾病的布-加(Budd-Chiari)综合征的临床特点。方法回顾性分析2002—2008年在本院诊断为布加综合征的48例患者的临床资料,分析其病因。结果48例患者中37例为原发性布-加综合征,仅11例患者系由其他具有较隐匿原发疾病所继发的布加综合征。其中以肝细胞癌居多。临床多以腹水、上消化道大出血等门脉高压症状为首发表现。治疗主要采取畅通管腔及针对原发病的治疗。结论以布-加综合征为首发症状、原发疾病隐匿的患者不常见,应引起重视。 Objective To analyze Clinical features of secondary Budd -Chiari syndrome (B-CS). Methods The clinical etidogy and features of 48 patients who were diagnosed B-CS in West China Hospital of Sichuan University between 2002 and 2008 were analyzed by retrospective study. Results There are 37 primary as 13-CS cases and 11 secondary cases. Most of these 11 cases showed portal hypertension symptom, such as ascites and upper digestive tract hemorrhage,as the first symptom. Hepatocellular carcinoma is discovered as the main primary disease of these secondary cases. Conclusion Secondary B-CS is uncommon, more attention should he paid to discover the primary disease as soon as Dossible.
出处 《肝脏》 2009年第2期108-110,共3页 Chinese Hepatology
关键词 布-加综合征 肝细胞癌 门静脉高压 Budd-Chiari syndrome Hepatocellular carcinoma Portal hypertention
  • 相关文献

参考文献3

二级参考文献32

  • 1[1]Valla DC.The diagnosis and management of the Budd-Chiari syndrome:consensus and controversies.Hepatology 2003; 38:793-803
  • 2[2]Okuda K.Inferior vena cava thrombosis at its hepatic portion (obliterative hepatocavopathy).Semin Liver Dis 2002; 22:15-26
  • 3[3]Denninger MH,Chait Y,Casadevall N,Hillaire S,Guillin MC,Bezeaud A,Erlinger S,Briere J,Valla D.Cause of portal or hepatic venous thrombosis in adults:the role of multiple concurrent factors.Hepatology 2000; 31:587-591
  • 4[4]Janssen HL,Meinardi JR,Vleggaar FP,van Uum SH,Haagsma EB,van Der Meer FJ,van Hattum J,Chamuleau RA,Adang RP,Vandenbroucke JP,van Hoek B,Rosendaal FR.Factor V Leiden mutation,prothrombin gene mutation,and deficiencies in coagulation inhibitors associated with Budd-Chiari syndrome and portal vein thrombosis:results of a casecontrol study.Blood 2000; 96:2364-2368
  • 5[5]Hirshberg B,Shouval D,Fibach E,Friedman G,Ben-Yehuda D.Flow cytometric analysis of autonomous growth of erythroid precursors in liquid culture detects occult polycythemia vera in the Budd-Chiari syndrome.J Hepatol 2000; 32:574-578
  • 6[6]Anger BR,Seifried E,Scheppach J,Heimpel H.Budd-Chiari syndrome and thrombosis of other abdominal vessels in the chronic myeloproliferative diseases.Klin Wochenschr 1989; 67:818-825
  • 7[7]Valla D,Casadevall N,Lacombe C,Varet B,Goldwasser E,Franco D,Maillard JN,Pariente EA,Leporrier M,Rueff B.Primary myeloproliferative disorder and hepatic vein thrombosis.A prospective study of erythroid colony formation in vitro in 20 patients with Budd-Chiari syndrome.Ann Intern Med 1985; 103:329-334
  • 8[8]Pagliuca A,Mufti GJ,Janossa-Tahernia M,Eridani S,Westwood NB,Thumpston J,Sawyer B,Sturgess R,Williams R.In vitro colony culture and chromosomal studies in hepatic and portal vein thrombosis--possible evidence of an occult myeloproliferative state.Q J Med 1990; 76:981-989
  • 9[9]Wanless IR,Peterson P,Das A,Boitnott JK,Moore GW,Bernier V.Hepatic vascular disease and portal hypertension in polycythemia vera and agnogenic myeloid metaplasia:a clinicopathological study of 145 patients examined at autopsy.Hepatology 1990; 12:1166-1174
  • 10[10]Janssen HL,Meinardi JR,Vleggaar FP,van Uum SH,Haagsma EB,van Der Meer FJ,van Hattum J,Chamuleau RA,Adang RP,Vandenbroucke JP,van Hoek B,Rosendaal FR.Factor V Leiden mutation,prothrombin gene mutation,and deficiencies in coagulation inhibitors associated with Budd-Chiari syndrome and portal vein thrombosis:results of a casecontrol study.Blood 2000; 96:2364-2368

共引文献52

同被引文献12

引证文献1

二级引证文献3

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部