The differential diagnoses for severe enteropathy or severely damaged small intestinal mucosa.

Q3 Medicine
Chao Ling Aran Jian, David T S Hayman, Bruce Lockett, Kamran Rostami
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Abstract

Aim: The aim of this study was to explore the aetiology of severe duodenal mucosal abnormality in consecutive patients who underwent gastroscopy and duodenal biopsy over the past 10 years.

Background: A range of differential diagnoses have been reported for severe duodenal architectural distortion.

Methods: Clinical and laboratory data of all the patients with severe duodenal architectural distortion diagnosed at MidCentral District Health Board (DHB), New Zealand were collected and statistically analysed. Ninety-five percent confidence intervals (CI) are shown.

Results: Between September 2009 and April 2019, 229 patients were diagnosed with severe enteropathy. The median patient age was 41 years (range 6-83 years). Two hundred and twenty-four of these patients (97.8%, 95.0-99.3%) were diagnosed with coeliac disease (CeD), with one of these patients having gluten induced T-cell lymphoma. From the remaining five patients, one had a diagnosis of tropical sprue and four did not have a clear aetiology. There were 180 patients from 191 (94.2%, 89.9-97.1%) with at least one positive coeliac marker, all with a diagnosis of CeD. Eleven patients (5.8% of 191, 2.9-10.1%) had negative markers for both tissue transglutaminase IgA (tTG-IgA) and IgA-endomysial antibodies (EMA-IgA) with six having a diagnosis of seronegative CeD.

Conclusion: Although the spectrum of histological changes in CeD may range from normal to a flat mucosa, severe duodenal architectural distortion seems to occur mainly in CeD. Idiopathic enteropathy was recorded as the second but by far less frequent presentation of severe enteropathy. This study highlights that infection and other aetiologies are rarely implicated in severe enteropathy, with one case (0.4%) of refractory CeD/T-cell lymphoma.

严重肠病或小肠黏膜严重损伤的鉴别诊断。
目的:本研究的目的是探讨在过去10年中连续接受胃镜检查和十二指肠活检的患者严重十二指肠黏膜异常的病因。背景:一系列的鉴别诊断已报道严重的十二指肠结构扭曲。方法:收集新西兰中央区卫生局(DHB)诊断的所有严重十二指肠结构畸形患者的临床和实验室资料,并进行统计学分析。95%置信区间(CI)显示。结果:2009年9月至2019年4月,229例患者被诊断为严重肠病。患者年龄中位数为41岁(范围6-83岁)。其中224名患者(97.8%,95.0-99.3%)被诊断为乳糜泻(CeD),其中1名患者患有麸质诱导的t细胞淋巴瘤。其余5例患者中,1例诊断为热带口疮,4例病因不明。191例患者中有180例(94.2%,89.9-97.1%)至少有一个乳糜泻标志物阳性,均诊断为CeD。11例患者(191例中占5.8%,2.9-10.1%)组织转谷氨酰胺酶IgA (tTG-IgA)和IgA-肌内膜抗体(EMA-IgA)标志物均为阴性,其中6例诊断为CeD血清阴性。结论:虽然CeD的组织学变化范围从正常到扁平,但严重的十二指肠结构扭曲似乎主要发生在CeD中。特发性肠病被记录为严重肠病的第二种但远不常见的表现。该研究强调,感染和其他病因很少与严重肠病有关,只有1例(0.4%)难治性CeD/ t细胞淋巴瘤。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
2.30
自引率
0.00%
发文量
29
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