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Clinical manifestations and gastrointestinal pathology in 40 patients with autoimmune enteropathy

机译:40例自身免疫肠病患者的临床表现和胃肠道病理学

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Autoimmune enteropathy (AIE) is a rare condition that may affect pediatric and adult patients, frequently associated with primary immunodeficiencies. We performed a retrospective study on clinical and histological findings from 40 AIE patients. Histological presentation showed a prevalent celiac disease pattern (50%), followed by the mixed pattern (35%), independently of age, chronic active duodenitis (10%), and GVHD-like pattern (5%). Patients with primary immunodeficiencies (24/40) presented mainly with the celiac disease pattern (72.2% versus 22.2%; p < .0001), while patients without primary immunodeficiencies presented with a mixed histological pattern (61.1% versus 13.6%; p < .0001). Our study shows that the prevalent histological presentation is the celiac disease-like pattern, independently of age, and, for the first time, that the histological presentation of AIE differs significantly between patients with and without primary immunodeficiencies. These findings may be helpful for more precise and timely diagnosis and management of this rare disorder.
机译:自身免疫肠病(AIE)是一种罕见的病症,可能会影响儿科和成人患者,经常与原发性免疫缺乏相关。我们对40名艾德患者的临床和组织学发现进行了回顾性研究。组织学介绍表现出普遍的乳糜泻模式(50%),其次是混合图案(35%),独立于年龄,慢性活性十二核炎(10%)和GVHD样图案(5%)。主要免疫缺乏症(24/40)的患者主要用乳糜泻模式(72.2%对22.2%; p <.0001),而没有混合组织学模式的患者没有初级免疫缺乏(61.1%对13.6%; p <。 0001)。我们的研究表明,普遍的组织学呈现是腹腔疾病样式,独立于年龄,并且是第一次,AIE的组织学呈现在患有和没有初级免疫缺乏的患者之间的显着不同。这些发现可能有助于对这种罕见疾病的更精确和及时的诊断和管理有所帮助。

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