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Dubin-Johnson综合征的病理学特征 被引量:17

Clinical pathology of Dubin-Johnson syndrome
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摘要 目的探讨Dubin-Johnson综合征(Dubin-Johnson syndrome,DJS)病人肝细胞内色素颗粒的本质。方法应用光镜、组织化学、免疫组织化学和电镜技术对肝细胞内色素颗粒进行探讨及其对S—100蛋白和HMB45的表达。结果组织学检查显示肝小叶结构正常,肝细胞内有大量棕褐色颗粒沉着,尤以小叶中央区明显。组织化学染色和超微结构观察结果证实色素颗粒具有脂褐素和黑色素的特征,免疫组织化学染色证实为黑色素。结论DJS病人肝细胞内色素颗粒为脂褐素一黑色素复合物。 Objective To investigate the property of pigment granules in the hepatocytes in patients with DubinJohnson syndrome. Method Light microscopy, histochemical, immnohistochemical and electron microscopy techniques were used to study the pigment glanules and the expression of S-100 protein and HMB45 in hepatocytes. Results Histological examination revealed normal lobular architecture and the abundont brown pigments which were chief'ly seen in the centrilobular zone hepatocytes. The pigment granules were evidenced to have the characterization of both lipofuscin and melanin by histochemical staining and ultrastructural studies and to have the featurts of the melanin by immnohistochemical staining. Conclusions The results suggest that the pigment grannies are lipfuscin-melanin complex in the hepatocytes in patients with Dubin-Johnson syndrome.
出处 《中华肝脏病杂志》 CAS CSCD 2000年第1期45-47,共3页 Chinese Journal of Hepatology
关键词 免疫组织化学 病理学 超微结构 DJS综合征 Jaundice, chronic iniopathic Histochemistry Immnohistochendsny Pathology, clinical Ultrastructure
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参考文献3

  • 1陈希陶 张学庸.Dubin-Johnson综合征19例报告[J].实用内科杂志,1983,3:138-139.
  • 2纪小龙,诊断免疫组织化学,1997年,85页
  • 3陈希陶,实用内科杂志,1983年,3卷,138页

同被引文献63

  • 1Qi-Xia Wang,Li Yan,Xiong Ma.Autoimmune Hepatitis in the Asia-Pacific Area[J].Journal of Clinical and Translational Hepatology,2018,6(1):48-56. 被引量:22
  • 2Mamun-Al Mahtab,Md. Fazal Karim,Salimur Rahman,Abul Barkat Muhammad Adnan.Dubin-Johnson syndrome with systemic lupus erythematosus: a case report[J].Hepatobiliary & Pancreatic Diseases International,2006,5(4):617-619. 被引量:6
  • 3赵国根,刘雁,陈群伟.Dubin-Johnson综合征七例和Rotor综合征二例的临床分析[J].中华传染病杂志,2004,22(4):279-281. 被引量:9
  • 4陈益平,汪洪姣,徐志伟,卢朝升,陈一华,张桂莲,方周溪.肝活检病理检查在肝脏疾病的临床应用[J].实用儿科临床杂志,2004,19(11):1000-1001. 被引量:3
  • 5蒯宝林 张远炎 等.Dubin-Johnson综合征2例[J].临床与实验病理学杂志,1999,15(3):259-260.
  • 6Cao M, Loe DW, Grant CE, et al. Reconstitution of ATP-dependent leukotriene C4 transport by co-expression of both halfmolecules of human muhidrug resistance protein in insect cells [ J]. J Biol chem, 1996,271:27782-27787.
  • 7Shift ER, Sorrell MF, Maddrey NC. Schiff diseases of the liver bed [ M ]. Philadelphia: Lippincott-Rave publishers, 1999,17 ( 192 ) :919- 935.
  • 8Verona Matema, Hermannlage. Homozygous mutation Arg768Trp in the ABC-transporter enxoding gene MRP2-/CMOAT/ABCC2 causes Dubin Johnson syndrome in the causion patient [ J]. J Hum Genet ,2003,48: 484.
  • 9WADA M,TOH S,TANIGUCHI K,et al. Mutations in the canalicular multispecific organic anion transporter (cMOAT)gene,a novel ABC transporter,in patients with hyperbilirubinemia II/Dubin Johnson syndrome [J]. Human Molecular Genetics, 1998,7(2)203-207.
  • 10B U CHLER M,K O NIG J,BROM M,et al. cDNA cloning of the hepatocyte canalicular isoform of the multidrug resistance protein,cMrp,reveals a novel conjugate export pump deficient in hyperbiliiubinemic mu- rant rats[J]. J Biol Chem,1996,271(25):15091-15098.

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