Bonamico Margherita, Thanasi Enina, Mariani Paolo, Nenna Raffaella, Luparia Rita Pia Lara, Barbera Cristiana, Morra Isabella, Lerro Pietro, Guariso Graziella, De Giacomo Costantino, Scotta Serenella, Pontone Stefano, Carpino Francesco, Magliocca Fabio Massimo
Department of Paediatrics, University La Sapienza of Rome, Rome, Italy.
J Pediatr Gastroenterol Nutr. 2008 Nov;47(5):618-22. doi: 10.1097/mpg.0b013e3181677d6e.
Celiac disease (CD)-related lesions have been reported in duodenal bulb biopsies, sometimes the bulb mucosa being the only one affected. The aim was to verify in a significant series whether histological lesions are always present in the bulb of celiac patients, what is the prevalence of lesions when isolated to the bulb, and if similar lesions are present in nonceliac subjects.
We studied 665 children with CD (241 males, range 9 months-15 years, 8 months), at diagnosis on a gluten-containing diet, and 348 age- and sex-matched gastroenterological controls submitted to upper endoscopy for gastroenterological complaints. During endoscopy, multiple biopsies (1 bulb and 4 distal duodenum samples) were taken. Anti-endomysium antibodies were evaluated by immunofluorescence method, anti-human tissue-transglutaminase antibodies by an enzyme-linked immunosorbent assay or radioimmunoassay. Human leukocyte antigen-DRB1, -DQA1, and -DQB1 genes were typed by polymerase chain reaction sequence-specific primers repeat method.
In all of the patients with CD, histological lesions were present in the bulb sample; in 16 of them, the lesions were present only in the bulb. Patchy villous atrophy was found in 20 children. All of the patients with CD were anti-endomysium and/or antitransglutaminase positive. The controls showed neither autoantibody positivity nor mucosal changes compatible with CD.
This study demonstrated that CD-related histological lesions are always present in the bulb; sometimes this specific site is the only one affected. Therefore, we suggest taking 2 biopsies from the bulb and 2 from the distal duodenum for CD diagnosis.
十二指肠球部活检中已报告有乳糜泻(CD)相关病变,有时球部黏膜是唯一受累部位。本研究旨在通过一个具有统计学意义的队列,验证乳糜泻患者球部是否总是存在组织学病变,孤立于球部的病变患病率是多少,以及非乳糜泻受试者是否存在类似病变。
我们研究了665例诊断时正在食用含麸质饮食的CD患儿(男241例,年龄范围9个月至15岁8个月),以及348例因胃肠疾病症状接受上消化道内镜检查、年龄和性别匹配的胃肠病学对照者。在内镜检查期间,采集多个活检样本(1个球部样本和4个十二指肠远端样本)。通过免疫荧光法评估抗肌内膜抗体,通过酶联免疫吸附测定或放射免疫测定评估抗组织转谷氨酰胺酶抗体。通过聚合酶链反应序列特异性引物重复法对人白细胞抗原-DRB1、-DQA1和-DQB1基因进行分型。
所有CD患者的球部样本均存在组织学病变;其中16例患者的病变仅存在于球部。20例患儿发现有斑片状绒毛萎缩。所有CD患者抗肌内膜和/或抗转谷氨酰胺酶均呈阳性。对照组既无自身抗体阳性,也无与CD相符的黏膜改变。
本研究表明,CD相关的组织学病变总是存在于球部;有时这个特定部位是唯一受累部位。因此,我们建议在诊断CD时,从球部取2个活检样本,从十二指肠远端取2个活检样本。