自身免疫性肠病合并自身免疫性肝炎1例

IF 2.1 4区 医学 Q3 GASTROENTEROLOGY & HEPATOLOGY Journal of Gastrointestinal and Liver Diseases Pub Date : 2023-06-22 DOI:10.15403/jgld-4624
Francisca Correia, Isabel Garrido, Vanessa Chaves, Armando Peixoto, Joanne Lopes, Guilherme Macedo, Jorge Almeida
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引用次数: 0

摘要

一名74岁的女性因体重减轻、腹痛和腹泻入院一年。血液检查显示转氨酶升高、胆汁淤积和高胆红素血症。胶囊内窥镜显示广泛分散的淋巴管扩张,短绒毛和糜烂在空肠和回肠。小肠粘膜活检组织学检查显示严重的粘膜萎缩和隐窝增生,未见明显的上皮内淋巴细胞增多。临床表现,对无麸质饮食缺乏反应,内窥镜和组织病理学结果与自身免疫性肠病一致。同时还诊断为自身免疫性肝炎。患者在开始使用泼尼松龙和硫唑嘌呤治疗后表现出明显的改善。据我们所知,这是首例自身免疫性肠病同时诊断为自身免疫性肝炎的病例。
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A Rare Case of Autoimmune Enteropathy Associated with Autoimmune Hepatitis.

A 74-year-old woman was admitted for weight loss, abdominal pain and diarrhea for a year. Blood tests showed elevated transaminases, cholestasis and hyperbilirubinemia. Capsule endoscopy revealed extensively scattered lymphangiectasias, shortened villi and erosions in the jejunum and ileum. The histological examination of the small bowel mucosa biopsies evidenced severe mucosal atrophy and crypt hyperplasia, without significant intraepithelial lymphocytosis. The clinical picture, lack of response to a gluten-free diet and endoscopic and histopathologic findings were compatible with autoimmune enteropathy. Simultaneously, autoimmune hepatitis was also diagnosed. The patient showed significant improvement after starting treatment with prednisolone and azathioprine. To our knowledge, this is the first case of autoimmune enteropathy diagnosed simultaneously with autoimmune hepatitis.

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来源期刊
CiteScore
3.20
自引率
0.00%
发文量
61
审稿时长
6-12 weeks
期刊介绍: The Journal of Gastrointestinal and Liver Diseases (formerly Romanian Journal of Gastroenterology) publishes papers reporting original clinical and scientific research, which are of a high standard and which contribute to the advancement of knowledge in the field of gastroenterology and hepatology. The field comprises prevention, diagnosis and management of gastrointestinal and hepatobiliary disorders, as well as related molecular genetics, pathophysiology, and epidemiology. The journal also publishes reviews, editorials and short communications on those specific topics. Case reports will be accepted if of great interest and well investigated.
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