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疑似肝脏局限性肉芽肿伴多血管炎

Suspected Hepatically Localized Granulomatosis with Polyangiitis.

作者信息

Yamamoto Toshiki, Ryuzaki Hitomi, Kobayashi Shun, Ohshiro Shu, Ogawa Masahiro, Tanaka Naohide, Gotoda Takuji, Moriyama Mitsuhiko, Kinukawa Noriko, Sugitani Masahiko, Notohara Kenji

机构信息

Division of Gastroenterology and Hepatology, Department of Medicine, Nihon University School of Medicine, Japan.

Department of Pathology, Nihon University School of Medicine, Japan.

出版信息

Intern Med. 2018 Jun 1;57(11):1583-1590. doi: 10.2169/internalmedicine.9724-17. Epub 2018 Feb 9.

Abstract

The patient was a 72-year-old woman whose alkaline phosphatase levels had been elevated since she was 56 years old. Liver biopsies obtained when the patient was 64 and 66 years of age led to a suspicion of cholangitis caused by vasculitis. Furthermore, proteinase-3 anti-neutrophil cytoplasmic antibody positivity led to a suspicion of granulomatosis with polyangiitis, but subjective symptoms and disorders in other organs were absent, so this suspicion was not confirmed. Cholangitis caused by vasculitis rarely occurs without vasculitis in other organs. We herein report this case in which we obtained distinctive laparoscopic and imaging findings that raised suspicions of liver circulatory failure.

摘要

该患者为一名72岁女性,自56岁起碱性磷酸酶水平就一直升高。患者64岁和66岁时进行的肝脏活检怀疑是由血管炎引起的胆管炎。此外,蛋白酶3抗中性粒细胞胞浆抗体呈阳性,怀疑是肉芽肿性多血管炎,但缺乏主观症状和其他器官的病变,因此这一怀疑未得到证实。由血管炎引起的胆管炎很少在其他器官没有血管炎的情况下发生。我们在此报告该病例,在该病例中我们获得了独特的腹腔镜检查和影像学结果,引发了对肝循环衰竭的怀疑。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/76b8/6028689/238722df691c/1349-7235-57-1583-g001.jpg

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