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小儿乳糜泻的诊断

Diagnosis of celiac disease in pediatric patients.

作者信息

Murray Joseph A, Rashtak Shadi, Rubio-Tapia Alberto

出版信息

Nat Rev Gastroenterol Hepatol. 2009 May;6(5):260-2. doi: 10.1038/nrgastro.2009.58.

DOI:10.1038/nrgastro.2009.58
PMID:19404264
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3896877/
Abstract

Children and adolescents with untreated celiac disease display disease-related, histological alterations in the duodenal bulb, according to a new study. In 16 of the 665 patients enrolled in the study, lesions were confined to the duodenal bulb.

摘要

一项新研究表明，未经治疗的乳糜泻儿童和青少年在十二指肠球部会出现与疾病相关的组织学改变。在该研究纳入的665名患者中，有16名患者的病变局限于十二指肠球部。

相似文献

1
Diagnosis of celiac disease in pediatric patients.小儿乳糜泻的诊断
Nat Rev Gastroenterol Hepatol. 2009 May;6(5):260-2. doi: 10.1038/nrgastro.2009.58.
2
Bulb biopsies for the diagnosis of celiac disease in pediatric patients.用于儿科患者乳糜泻诊断的球部活组织检查。
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Diagnostic bulb biopsies in celiac disease.乳糜泻的诊断性球部活检。
Gastrointest Endosc. 2009 Feb;69(2):388-9; author reply 390. doi: 10.1016/j.gie.2008.06.014.
4
Importance of duodenal bulb biopsies in children for diagnosis of celiac disease in clinical practice.十二指肠球部活检在儿童乳糜泻临床诊断中的重要性。
BMC Gastroenterol. 2009 Oct 16;9:78. doi: 10.1186/1471-230X-9-78.
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Comparison of the Marsh-Oberhuber classification with a new grading system in identifying patients with latent celiac disease.比较马什-奥伯胡伯分类法与一种新的分级系统在识别潜在乳糜泻患者中的应用。
Minerva Gastroenterol Dietol. 2010 Dec;56(4):371-5.
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The problem of biopsies in the diagnosis of celiac disease.
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Not everything is celiac disease.并非所有情况都是乳糜泻。
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Diagnostic duodenal bulb biopsy in celiac disease.乳糜泻的十二指肠球部诊断性活检
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9
Duodenal bulb histological analysis should be standard of care when evaluating celiac disease in children.在评估儿童乳糜泻时，十二指肠球部组织学分析应作为标准治疗手段。
Pediatr Dev Pathol. 2014 Sep-Oct;17(5):339-43. doi: 10.2350/14-03-1451-OA.1. Epub 2014 Jul 30.
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Scalloped duodenal folds in childhood celiac disease.儿童乳糜泻中的十二指肠扇形皱襞
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引用本文的文献

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The identification of celiac disease in asymptomatic children: the Generation R Study.无症状儿童乳糜泻的鉴定：生育队列研究。
J Gastroenterol. 2018 Mar;53(3):377-386. doi: 10.1007/s00535-017-1354-x. Epub 2017 Jun 6.

本文引用的文献

1
Duodenal bulb biopsies in celiac disease: a multicenter study.乳糜泻患者十二指肠球部活检：一项多中心研究。
J Pediatr Gastroenterol Nutr. 2008 Nov;47(5):618-22. doi: 10.1097/mpg.0b013e3181677d6e.
2
Mucosal atrophy in celiac disease: extent of involvement, correlation with clinical presentation, and response to treatment.乳糜泻中的黏膜萎缩：累及范围、与临床表现的相关性及对治疗的反应。
Clin Gastroenterol Hepatol. 2008 Feb;6(2):186-93; quiz 125. doi: 10.1016/j.cgh.2007.10.012. Epub 2007 Dec 21.
3
Celiac disease.乳糜泻
N Engl J Med. 2007 Oct 25;357(17):1731-43. doi: 10.1056/NEJMra071600.
4
American Gastroenterological Association (AGA) Institute technical review on the diagnosis and management of celiac disease.美国胃肠病学会（AGA）研究所关于乳糜泻诊断与管理的技术综述。
Gastroenterology. 2006 Dec;131(6):1981-2002. doi: 10.1053/j.gastro.2006.10.004.
5
Variability of histologic lesions in relation to biopsy site in gluten-sensitive enteropathy.麸质敏感性肠病中组织学病变与活检部位的相关性变异
Am J Gastroenterol. 2005 Jan;100(1):177-85. doi: 10.1111/j.1572-0241.2005.40669.x.
6
Guideline for the diagnosis and treatment of celiac disease in children: recommendations of the North American Society for Pediatric Gastroenterology, Hepatology and Nutrition.儿童乳糜泻诊断与治疗指南：北美儿科胃肠病、肝病和营养学会的建议
J Pediatr Gastroenterol Nutr. 2005 Jan;40(1):1-19. doi: 10.1097/00005176-200501000-00001.
7
Patchy villous atrophy of the duodenum in childhood celiac disease.儿童乳糜泻时十二指肠的斑片状绒毛萎缩
J Pediatr Gastroenterol Nutr. 2004 Feb;38(2):204-7. doi: 10.1097/00005176-200402000-00019.
8
STUDIES OF CELIAC SPRUE. IV. THE RESPONSE OF THE WHOLE LENGTH OF THE SMALL BOWEL TO A GLUTEN-FREE DIET.乳糜泻研究。IV. 小肠全长对无麸质饮食的反应。
Gastroenterology. 1964 Dec;47:573-89.
9
Duodeno-jejunal biopsy in the investigation of children with coeliac disease.十二指肠空肠活检在乳糜泻患儿检查中的应用
Q J Med. 1962 Jan;31:125-40.
10
Small bowel biopsy for malabsorption: comparison of the diagnostic adequacy of endoscopic forceps and capsule biopsy specimens.用于吸收不良的小肠活检：内镜钳取活检与胶囊活检标本诊断充分性的比较
Br Med J (Clin Res Ed). 1985 Sep 21;291(6498):769-72. doi: 10.1136/bmj.291.6498.769.