Bhatnagar Shinjini, Gupta Sidhartha Datta, Mathur Meera, Phillips Alan D, Kumar Ramesh, Knutton Stuart, Unsworth David J, Lock Robert J, Natchu Uma C M, Mukhopadhyaya Sanjay, Saini Savita, Bhan Maharaj K
Centre for Diarrhoeal Diseases and Nutrition Research, Department of Pediatrics, All India Institute of Medical Sciences, Ansari Nagar, New Delhi, India.
J Pediatr Gastroenterol Nutr. 2005 Aug;41(2):204-9. doi: 10.1097/01.mpg.0000172261.24115.29.
In developed countries, small bowel histology in coeliac disease is a spectrum, ranging from normal with increased intraepithelial lymphocytes to the classic flat mucosa. In developing countries, mild to moderate enteropathies in children with chronic diarrhea and growth failure are assumed to be caused by tropical sprue, persistent infections, or malnutrition with bacterial overgrowth. We report the prevalence and histology of coeliac disease in children with chronic diarrhea at a tertiary referral hospital in North India.
Two hundred fifty-nine children with symptoms indicating coeliac disease attended the All India Institute of Medical Sciences. Histology was graded after a modified Marsh classification. Serum immunoglobulin A anti-endomysial antibodies (AEA) were assayed using indirect immunofluorescence. Subjects with abnormal histology and positive AEA were put on a gluten free diet (GFD). Coeliac disease was diagnosed on small intestinal biopsy changes and a clinical response to a GFD.
Severe enteropathies were present in 63 (24%) subjects, and 58 (92%) responded to a GFD. Sixty-six (25%) had moderate histologic changes, 61 responding to a GFD. AEA was positive in 56 of 63 patients with severe and 65 of 66 with moderate enteropathies. Fifty-seven children had mild enteropathies, and 19 of 20 with positive AEA responded clinically to a GFD.
Coeliac disease is more common than previously believed. It presents a variable histology, and diagnoses may be missed or delayed if based only on severe enteropathies. Serology is a useful adjunct to diagnosis, and diagnostic criteria need to be developed appropriately for coeliac disease in developing countries despite limited facilities.
在发达国家,乳糜泻的小肠组织学表现呈谱系变化,从上皮内淋巴细胞增多的正常表现到典型的扁平黏膜。在发展中国家,慢性腹泻和生长发育迟缓儿童的轻至中度肠病被认为是由热带口炎性腹泻、持续性感染或伴有细菌过度生长的营养不良所致。我们报告了印度北部一家三级转诊医院慢性腹泻儿童中乳糜泻的患病率及组织学情况。
259名有乳糜泻症状的儿童前往全印度医学科学研究所就诊。组织学根据改良的马什分类法进行分级。采用间接免疫荧光法检测血清免疫球蛋白A抗肌内膜抗体(AEA)。组织学异常且AEA阳性的受试者接受无麸质饮食(GFD)。根据小肠活检结果及对GFD的临床反应诊断乳糜泻。
63名(24%)受试者存在严重肠病,其中58名(92%)对GFD有反应。66名(25%)有中度组织学改变,61名对GFD有反应。63名严重肠病患者中有56名AEA阳性,66名中度肠病患者中有65名AEA阳性。57名儿童有轻度肠病,20名AEA阳性者中有19名对GFD有临床反应。
乳糜泻比之前认为的更为常见。其组织学表现多样,若仅依据严重肠病进行诊断,可能会漏诊或延误诊断。血清学检查对诊断有辅助作用,尽管设施有限,但仍需为发展中国家的乳糜泻制定合适的诊断标准。