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一例与类风湿关节炎相关的特发性门静脉高压症。

A case of idiopathic portal hypertension associated with rheumatoid arthritis.

作者信息

Sasajima Tomomi, Suzuki Tomohiro, Mori Kenji, Ichii Osamu, Tai Mayumi, Ochiai Hironobu, Ejiri Yutaka, Watanabe Hiroshi, Ohira Hiromasa, Obara Katsutoshi, Sato Yukio

机构信息

Department of Internal Medicine II, Fukushima Medical University School of Medicine, 1 Hikarigaoka, Fukushima, 960-1295, Japan.

出版信息

Mod Rheumatol. 2006;16(2):92-6. doi: 10.1007/s10165-006-0456-8.

Abstract

A 53-year-old woman who had been diagnosed with rheumatoid arthritis was found to have thrombocytopenia, splenomegaly, and gastric varices. She was diagnosed as having idiopathic portal hypertension on the basis of liver biopsy and angiography. Treatment with prednisolone was not sufficiently effective for thrombocytopenia. After transabdominal devascularization with splenectomy, thrombocytopenia subsided and gastric varices disappeared. In this case, the autoimmune mechanism as well as hypersplenism was suspected of being involved in the mechanism of thrombocytopenia.

摘要

一名53岁已被诊断为类风湿性关节炎的女性被发现患有血小板减少症、脾肿大和胃静脉曲张。根据肝脏活检和血管造影,她被诊断为特发性门静脉高压症。泼尼松龙治疗血小板减少症效果不佳。经腹去血管化脾切除术后,血小板减少症消退,胃静脉曲张消失。在这种情况下,怀疑自身免疫机制以及脾功能亢进参与了血小板减少症的发病机制。

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