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以轻度肠炎为病因的、以前未知原因的缺铁性贫血。

Mild enteropathy as a cause of iron-deficiency anaemia of previously unknown origin.

机构信息

Department of Gastroenterology, Hospital Universitari Mútua Terrassa and Research Foundation Mútua Terrassa, Barcelona, Spain.

出版信息

Dig Liver Dis. 2011 Jun;43(6):448-53. doi: 10.1016/j.dld.2010.12.003. Epub 2011 Jan 12.

DOI:10.1016/j.dld.2010.12.003
PMID:21233030
Abstract

BACKGROUND AND AIMS

We assessed whether mild enteropathy with negative coeliac serology may be gluten-dependent, and a cause of iron-deficiency anaemia. In cases not responding to gluten-free diet, the role of Helicobacter pylori infection was evaluated.

METHODS

55 consecutive unexplained iron-deficiency anaemia patients were included. In all of them we performed: HLA-DQ2/DQ8 coeliac genetic study, distal duodenum biopsies, and tests to assess H. pylori infection. A gluten-free diet or H. pylori eradication was used as indicated. Final diagnosis was established based on response to specific therapy after a 12-month follow-up period.

RESULTS

Histological findings were: (1) group A (positive genetics): 21 Marsh I, 2 Marsh IIIA, 12 normal; (2) group B (negative genetics): 16 Marsh I, 4 normal. Final diagnosis of anaemia in patients with enteropathy were: group A, gluten-sensitive enteropathy, 45%; H. pylori infection, 20%; gluten-sensitive enteropathy plus H. pylori, 10%; other, 10%; unknown, 15%; group B, gluten-sensitive enteropathy, 10%; H. pylori infection, 0% (1 non-eradicated case, 10%); non-steroidal anti-inflammatory drug intake, 20%; other, 20%; unknown, 40% (p=0.033).

CONCLUSIONS

Mild enteropathy is frequent in patients with unexplained iron-deficiency anaemia and negative coeliac serology. Most cases are secondary to either gluten-sensitive enteropathy or H. pylori infection, or both; however, there is also a substantial number of patients without a definitive diagnosis.

摘要

背景和目的

我们评估了伴有阴性乳糜泻血清学的轻度肠病是否可能与麸质有关,以及是否是缺铁性贫血的病因。在那些对无麸质饮食无反应的病例中,评估了幽门螺杆菌感染的作用。

方法

纳入了 55 例连续的不明原因缺铁性贫血患者。对所有患者均进行了以下检查:HLA-DQ2/DQ8 乳糜泻遗传研究、远端十二指肠活检以及评估幽门螺杆菌感染的检查。根据需要给予无麸质饮食或幽门螺杆菌根除治疗。根据 12 个月的随访期内对特定治疗的反应来确定最终诊断。

结果

组织学发现:(1)组 A(阳性遗传学):21 例 Marsh I,2 例 Marsh IIIA,12 例正常;(2)组 B(阴性遗传学):16 例 Marsh I,4 例正常。患有肠病的患者的贫血最终诊断为:组 A,乳糜泻相关肠病,45%;幽门螺杆菌感染,20%;乳糜泻相关肠病加幽门螺杆菌,10%;其他,10%;未知,15%;组 B,乳糜泻相关肠病,10%;幽门螺杆菌感染,0%(1 例未根除,10%);非甾体抗炎药摄入,20%;其他,20%;未知,40%(p=0.033)。

结论

在不明原因缺铁性贫血且乳糜泻血清学阴性的患者中,轻度肠病很常见。大多数病例继发于麸质敏感肠病或幽门螺杆菌感染,或两者同时存在;然而,也有相当数量的患者无法明确诊断。

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