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纯红细胞再生障碍性贫血及相关胸腺瘤。

Pure red cell aplasia and associated thymoma.

作者信息

Rosu Cristian, Cohen Sandra, Meunier Caroline, Ouellette Denise, Beauchamp Gilles, Rakovich George

机构信息

Division of Thoracic Surgery.

Division of Hematology.

出版信息

Clin Pract. 2011 Apr 1;1(1):e1. doi: 10.4081/cp.2011.e1. eCollection 2011 Mar 29.

Abstract

Pure red cell aplasia is a rare cause of anemia, caused by an absence of red blood cell precursors in the bone marrow. It is usually a paraneoplastic syndrome, associated most commonly with large-cell granular lymphocyte leukemia but also thymoma. For patients who present both pure red cell aplasia and thymoma, thymectomy leads to an initial remission of the aplasia in 30% of cases. However, sustained remission may require the addition of medications such as corticosteroids, cyclosporine, or cyclophosphamide. We present a case of pure red cell aplasia associated with a thymoma in an otherwise healthy 80 year-old woman.

摘要

纯红细胞再生障碍性贫血是一种罕见的贫血病因,由骨髓中缺乏红细胞前体所致。它通常是一种副肿瘤综合征,最常与大颗粒淋巴细胞白血病相关,但也与胸腺瘤有关。对于同时患有纯红细胞再生障碍性贫血和胸腺瘤的患者,胸腺切除术在30%的病例中可使再生障碍性贫血获得初始缓解。然而,持续缓解可能需要加用皮质类固醇、环孢素或环磷酰胺等药物。我们报告一例80岁健康女性患纯红细胞再生障碍性贫血合并胸腺瘤的病例。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f681/3981205/a232cbd868dc/cp-2011-1-e1-g001.jpg

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