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一例与红系发育异常/再生障碍的骨髓增生异常综合征相关的复发性多软骨炎。

A case of relapsing polychondritis associated with myelodysplastic syndrome with erythroid hypoplasia/aplasia.

作者信息

Heo Seong-Wook, Cho Kyu-Hyun, Ryu Jung-Il, Chung Seung-Hie, Kim Chae-Gi, Kim Sang-Gyung, Choe Jung-Yoon

机构信息

Department of Internal Medicine, Catholic University of Daegu School of Medicine, Daegu, Korea.

出版信息

Korean J Intern Med. 2003 Dec;18(4):251-4. doi: 10.3904/kjim.2003.18.4.251.

Abstract

Relapsing polychondritis (RP) is a rare multisystem disorder. Myelodysplastic syndrome (MDS) with erythroid hypoplasia/aplasia is a rare form of myelodysplasia. Several cases of RP associated with MDS have recently been described. However, RP associated with MDS with erythroid hypoplasia/aplasia has never been reported. There was only one case report of polymyalgia rheumatica associated with MDS with erythroid hypoplasia/aplasia. In this study, we report a 79-year-old patient with RP, who developed MDS subtype refractory anemia (RA) with erythroid hypoplasia/aplasia, a very characteristic subtype of MDS.

摘要

复发性多软骨炎(RP)是一种罕见的多系统疾病。伴有红系发育不全/再生障碍的骨髓增生异常综合征(MDS)是骨髓增生异常的一种罕见形式。最近已有几例RP与MDS相关的病例报道。然而,RP与伴有红系发育不全/再生障碍的MDS相关的情况从未被报道过。仅有一例风湿性多肌痛与伴有红系发育不全/再生障碍的MDS相关的病例报告。在本研究中,我们报告了一名79岁的RP患者,该患者发展为伴有红系发育不全/再生障碍的MDS亚型难治性贫血(RA),这是MDS一种非常典型的亚型。

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