Jian Chao Ling Aran, Hayman David T S, Lockett Bruce, Rostami Kamran
Department of Gastroenterology, MidCentral District Health Board, Palmerston North, New Zealand.
Molecular Epidemiology & Public Health Laboratory, School of Veterinary Science, Massey University, Palmerston North, New Zealand.
Gastroenterol Hepatol Bed Bench. 2023;16(2):181-187. doi: 10.22037/ghfbb.v16i2.2717.
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.
A range of differential diagnoses have been reported for severe duodenal architectural distortion.
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.
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.
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.
本研究旨在探讨过去10年中接受胃镜检查及十二指肠活检的连续性患者出现严重十二指肠黏膜异常的病因。
对于严重十二指肠结构扭曲已有一系列鉴别诊断的报道。
收集了新西兰中区卫生局(DHB)诊断为严重十二指肠结构扭曲的所有患者的临床和实验室数据,并进行了统计分析。给出了95%置信区间(CI)。
2009年9月至2019年4月期间,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例患者(97.8%,95.0 - 99.3%)被诊断为乳糜泻(CeD),其中1例患者患有麸质诱导的T细胞淋巴瘤。其余5例患者中,1例诊断为热带口炎性腹泻,4例病因不明。191例患者中有180例(94.2%,89.9 - 97.1%)至少有一项乳糜泻阳性标志物,均诊断为CeD。11例患者(191例中的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例诊断为血清阴性CeD。
虽然CeD的组织学变化范围可能从正常到扁平黏膜,但严重十二指肠结构扭曲似乎主要发生在CeD患者中。特发性肠病被记录为严重肠病的第二大病因,但到目前为止其出现频率要低得多。本研究强调,感染和其他病因很少与严重肠病相关,仅1例(0.4%)难治性CeD/T细胞淋巴瘤。