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英国免疫性血小板减少症登记处:成年原发性免疫性血小板减少症患者骨髓纤维化的回顾性评估及其与临床发现的相关性

United Kingdom immune thrombocytopenia registry: retrospective evaluation of bone marrow fibrosis in adult patients with primary immune thrombocytopenia and correlation with clinical findings.

作者信息

Rizvi Hasan, Butler Tom, Calaminici Mariarita, Doobaree Indraraj U, Nandigam Raghava C, Bennett Dimitri, Provan Drew, Newland Adrian C

机构信息

Department of Pathology, Barts Health NHS Trust, London, UK; Barts and The London School of Medicine and Dentistry, Queen Mary University London, London, UK.

出版信息

Br J Haematol. 2015 May;169(4):590-4. doi: 10.1111/bjh.13330. Epub 2015 Mar 5.

Abstract

Fibrosis has been reported in some patients with immune thrombocytopenia (ITP) treated with thrombopoietin receptor agonists (TPO-RA). However, fibrosis has also been reported in patients with various stages of ITP, who were TPO-RA treatment-naïve. In our study, we looked for fibrosis in bone marrow trephine biopsies taken at initial diagnosis from 32 adult patients with ITP. Ten of the 32 evaluated samples (31·25%) showed increased reticulin (Grade 1-2 on Bauermeister scale and Grade 0-1 on the European Consensus scale), which showed a positive correlation with ethnicity (0·3%) but did not correlate with disease severity, any clinical features or co-morbidities.

摘要

在一些接受血小板生成素受体激动剂(TPO-RA)治疗的免疫性血小板减少症(ITP)患者中已报告有纤维化情况。然而,在未接受过TPO-RA治疗的处于ITP不同阶段的患者中也有纤维化的报告。在我们的研究中,我们在32例成年ITP患者初诊时所取的骨髓活检组织中寻找纤维化情况。32份评估样本中有10份(31.25%)显示网硬蛋白增加(根据鲍ermeister分级为1 - 2级,根据欧洲共识分级为0 - 1级),其与种族呈正相关(0.3%),但与疾病严重程度、任何临床特征或合并症均无关联。

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