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钙视网膜蛋白在先天性无神经节细胞症中的表达特点及临床意义 被引量:4

Expression characteristics of calretinin in hirschsprung′s disease and its clinical significance
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摘要 目的探讨将钙视网膜蛋白(CR)用于诊断先天性无神经节细胞症(HD)的可行性。方法采用免疫组织化学法检测CR在50例HD(HD扩张段组、HD痉挛段组)和10例对照组结肠壁的表达,并与常规HE染色进行对比分析。用Image-Pro-Plus图文分析系统定量分析染色结果。结果 HD痉挛段组与对照组及HD扩张段组黏膜下层、肌层间CR表达的平均光密度值(MOD)差异均有统计学意义(P<0.01);HE染色扩张段肠壁神经丛中可见神经节细胞,痉挛段神经节细胞缺失,CR免疫组织化学染色与HE染色诊断结果一致;新生儿与年长儿HD痉挛段黏膜下层CR表达差异无统计学意义(P=0.816)。结论 CR免疫组织化学染色用于新生儿HD的诊断与传统方法比较具有明显优越性。 Objective To explore the feasibility of calretinin(CR) in the diagnosis of hirschsprung′s disease(HD).Methods Colons from 50 children with HD(HD spastic segments group and ecstatic segments group) and 10 controls were stained for CR by immunohistochemistry,and were compared with conventional HE staining,with Image-Pro-Plus analysis system for quantitative analysis of staining.Results There was a significant difference in the expression of calretinin mean optical density between HD spastic segments group and ecstatic segments group,normal control group(P0.01).Ganglion cells could be seen in ecstatic segments in HE stained section of intestinal nerve plexus,but lost in spastic segment,CR results of immunohistochemistry were consistent with HE staining results.Newborns and older children HD spastic segment submucosa had no significant difference in the expression of CR(P=0.816).Conclusion CR immunohistochemical staining for the diagnosis of neonatal HD has obvious advantages compared with traditional methods.
出处 《重庆医学》 CAS CSCD 北大核心 2012年第33期3468-3470,F0002,共4页 Chongqing medicine
基金 国家自然科学基金面上项目(30973136)
关键词 先天性无神经节细胞症 钙视网膜蛋白 免疫组织化学 hirschsprung′s disease calretinin immunohistochemistry
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参考文献12

  • 1Lwashita T, Kruger GM, Pardal R, et al. Hirsehsprung disease is linked to defects in neural crest stem cell func- tion[J]. Science, 2003,301 (5635) : 972-976.
  • 2Montedonico S,Cdceres P, Mufloz N, et al. Histochemical staining for intestinal dysganglionosis .. over 30 years expe- rience with more than 1 500 biopsies[J]. Pediatr Surg Int, 2011,27 (5) : 479-486.
  • 3杨小进,林传友,胡道松,殷光甫.外周蛋白和组织蛋白酶D在先天性巨结肠症中的表达[J].中华小儿外科杂志,2004,25(3):261-263. 被引量:9
  • 4Pacheco MC, Bove KE. Variability of acetylcholinesterase hyperinnervation patterns in distal rectal suction biopsy specimens in Hirschsprung disease [J]. Pediatr Dev Pathol, 2008,11 (4) : 274-282.
  • 5Nakao M, Suita S, Taguchi T, et al. Fourteen-year experi- ence of acetylcholinesterase staining for rectal mucosal bi- opsy in neonatal Hirschsprungrs disease[J]. J Pediatr Surg, 2001,36 (9) : 1357-1363.
  • 6Chentanez V,Chittmittrapap S,Cheepsoonthorn P, et al.New classification of histochemical staining patterns of acetylcholinesterase activity in rectal suction biopsy in Hirschsprung' s disease [J ]. Med Assoc Thai, 2000, 83 (10) .. 1196-1201.
  • 7Kapur RP, Reed RC, Finn LS, et al. Calretinin immunohis- tochemistry versus acetylcholinesterase histochemistry in the evaluation of suction rectal biopsies for Hirschsprung disease[J]. Pediatr Dev Pathol,2009,12(1) :6-15.
  • 8刘虎,徐兵.新生儿巨结肠诊断的现状与进展[J].医学综述,2010,16(16):2433-2435. 被引量:9
  • 9Holland SK, Hessler RB, Reid-Nicholson MD, et al. Utili- zation of peripherin and S-100 immunohistochemistry in the diagnosis of Hirschsprung disease[J]. Modern Pathol ogy,2010,23(9) :1173-1179.
  • 10Guinard-Samuel V, Bonnard A, De Lagausie P, et al. Cal- retinin immunohistochemistry: a simple and efficient tool to diagnose Hirschsprung disease[J]. Mod Pathol, 2009, 22(10) : 1379-1384.

二级参考文献37

共引文献22

同被引文献93

  • 1孙晓毅,王果,郭先娥,袁继炎,史慧芬.巨结肠类缘性疾病肛管测压、直肠黏膜活检和钡灌肠检查的意义[J].中华小儿外科杂志,2004,25(4):331-334. 被引量:13
  • 2周雪莲,陈飞波,欧弼悠,章许平,江米足.新生儿先天性巨结肠直肠肛管压力监测及其临床意义[J].中华儿科杂志,2004,42(9):681-683. 被引量:19
  • 3马永利,张传龙,吴小亚,陆国云.新生儿先天性巨结肠的早期诊断与治疗[J].临床医学,2007,27(2):33-35. 被引量:15
  • 4黄焱磊,郑珊,肖现民.直肠肛管测压对新生儿先天性巨结肠诊断意义的研究[J].临床小儿外科杂志,2007,6(3):3-5. 被引量:14
  • 5de Lorijn Fv Kremer LC,Reitsma JB, et al. Diagnostic tests in Hirschsprung disease: a systematic review [J]. J Pediatr Gastroenterol Nutr,2006,42(5) :496-505.
  • 6Martucciello G,Pini Prato A, Puri P, et al. Controversies concerning diagnostic guidelines for anomalies of the enteric nervous system: a report from the fourth International Symposium on Hirschsprung' s disease and related neurocristopathies[J]. J Pediatr Surg, 2005, 40 (10): 1527 1531.
  • 7Kessmann J. Hirschsprung' S disease: diagnosis and management[J]. Am Fam Physician,2006, 74(8): 1319-1322.
  • 8Moore SW, Johnson G. Acetylcholinesterase in Hirsehsprung' s disease[J]. Pediartr Surg Int,2005,21(4) :255-263.
  • 9eier-Ruge W, Lutterbeck PM, Herzog B, et al. Acetylcholinesterase activity in suction biopsies of the rectum in the diagnosis of Hirschsprung disease [J]. J Pediatr Surg , 1972,7(1):11-17.
  • 10Nakao M, Suita S, Taguchi T, et al.Fourteen-year experience of acetylcholinesterase staining for rectal mucosal biopsy in neonatal Hirschsprungs disease[J]. J Pediatr Surg 2001,36(9):1357-1363.

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