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系统性红斑狼疮骨髓胶样变性。

Gelatinous transformation of the bone marrow in systemic lupus erythematosus.

机构信息

Division of Rheumatology, Kameda Medical Center, Chiba 296-8602, Japan.

出版信息

Lupus. 2009 Oct;18(12):1108-11. doi: 10.1177/0961203309106344.

Abstract

Gelatinous transformation of the bone marrow is a rare disease characterised by a focal marrow hypoplasia, fat atrophy and accumulation of extracellular mucopolysaccharides abundant in hyaluronic acid, which is often associated with extreme malnutrition and weight loss. There are only two reports describing its association with systemic lupus erythematosus (SLE). One described underlying diseases in 155 cases of gelatinous transformation of the bone marrow and found one case with clinical diagnosis of SLE, but no clinical details were provided. The other described three SLE patients with gelatinous transformation of the bone marrow; however, two of these were cachectic and one was diagnosed with concomitant tuberculosis. We describe one active SLE patient without other comorbidities whose pancytopaenia was histologically confirmed as gelatinous transformation. The combination of high-dose steroid, intravenous immunoglobulin and mycophenolate mofetil improved the peripheral blood cytopaenia and reversed the bone marrow abnormalities.

摘要

骨髓胶样变性是一种罕见疾病,其特征为局灶性骨髓发育不良、脂肪萎缩和细胞外黏多糖(富含透明质酸)积聚,常与极度营养不良和体重减轻有关。仅有两份报告描述了其与系统性红斑狼疮(SLE)的关联。一份报告描述了 155 例骨髓胶样变性的基础疾病,发现一例临床诊断为 SLE,但未提供具体临床细节。另一份报告描述了三例 SLE 合并骨髓胶样变性患者;然而,其中两例为恶病质,一例并发肺结核。我们描述了一例无其他合并症的活动期 SLE 患者,其全血细胞减少症经组织学证实为骨髓胶样变性。大剂量类固醇、静脉注射免疫球蛋白和霉酚酸酯改善了外周血血细胞减少症,并逆转了骨髓异常。

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