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伴有自身免疫抗体的复发性嗜酸性粒细胞性胃肠炎

Eosinophilic Gastroenteritis with a Relapsing and Remitting Course with Presence of Autoimmune Antibodies.

作者信息

Fonseka Chathuranga Lakmal, Nanayakkara Sunali, Singhapura S D A L, Herath H M M, Bodinayake C K

机构信息

University Medical Unit, Teaching Hospital Karapitiya, Galle, Sri Lanka.

Faculty of Medicine, University of Ruhuna, Matara, Sri Lanka.

出版信息

Case Rep Med. 2020 Aug 18;2020:1745834. doi: 10.1155/2020/1745834. eCollection 2020.

Abstract

BACKGROUND

Eosinophilic gastroenteritis (EGE) is an uncommon disease characterized by eosinophilic infiltration of the digestive tract, which occurs due to an uncertain aetiology. Although autoimmune diseases can later present as EGE, it is unusual for EGE to have positive autoimmune antibodies without the presence of an overt autoimmune disease. We report a 38-year-old previously healthy man who presented with abdominal discomfort and loose stools with pleural and peritoneal effusions progressing over several weeks. His investigations revealed severe eosinophilia in peripheral blood and ascitic fluid, and a laparoscopic full-thickness biopsy from the ileum demonstrated infiltration of eosinophils in all three layers of the intestine. There were no clinical features or investigations suggestive of parasitic disease, other diseases associated with eosinophilia, or autoimmune disease. Further investigations showed a highly positive ANA, positive p-ANCA, but did not meet the criteria to diagnose a specific autoimmune disease. The eosinophilia responded to an elimination diet with gradual resolution of eosinophilia and effusions, and once it reappeared after introduction of a normal diet.

CONCLUSION

EGE presenting as peripheral blood and ascitic fluid eosinophilia with the presence of pleural and/or peritoneal effusions is uncommon. Eosinophilic gastroenteritis can be associated with autoantibody positivity without any evidence of overt autoimmune disease manifestations. Elimination diet can be used as a potential option to prevent recurrences of EGE.

摘要

背景

嗜酸性粒细胞性胃肠炎(EGE)是一种罕见疾病,其特征为消化道嗜酸性粒细胞浸润,病因不明。虽然自身免疫性疾病后期可表现为EGE,但EGE在无明显自身免疫性疾病的情况下出现自身免疫抗体阳性并不常见。我们报告一名38岁既往健康男性,他出现腹部不适和腹泻,伴有胸腔和腹腔积液,病程持续数周。他的检查显示外周血和腹水严重嗜酸性粒细胞增多,回肠腹腔镜全层活检显示肠道三层均有嗜酸性粒细胞浸润。没有临床特征或检查提示寄生虫病、其他与嗜酸性粒细胞增多相关的疾病或自身免疫性疾病。进一步检查显示抗核抗体(ANA)高度阳性、核周型抗中性粒细胞胞浆抗体(p-ANCA)阳性,但不符合诊断特定自身免疫性疾病 的标准。嗜酸性粒细胞增多对排除饮食有反应,嗜酸性粒细胞增多和积液逐渐消退,恢复正常饮食后嗜酸性粒细胞增多再次出现。

结论

以外周血和腹水嗜酸性粒细胞增多伴胸腔和/或腹腔积液为表现的EGE并不常见。嗜酸性粒细胞性胃肠炎可与自身抗体阳性相关,而无任何明显自身免疫性疾病表现的证据。排除饮食可作为预防EGE复发的一种潜在选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/79d7/7450306/c34371faf042/CRIM2020-1745834.001.jpg

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