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自然杀伤细胞白血病/淋巴瘤异基因骨髓移植后出现新月体形成和大量IgA沉积的肾病综合征。

Nephrotic syndrome with crescent formation and massive IgA deposition following allogeneic bone marrow transplantation for natural killer cell leukemia/lymphoma.

作者信息

Kimura Shinya, Horie Akeyo, Hiki Yoshiyuki, Yamamoto Chie, Suzuki Satoru, Kuroda Junya, Deguchi Masayo, Kato Gen-ichi, Karasuno Takahiro, Hiraoka Akira, Yoshikawa Toshikazu, Maekawa Taira

机构信息

Department of Transfusion Medicine, Kyoto University Hospital, Kyoto, Japan.

出版信息

Blood. 2003 May 15;101(10):4219-21. doi: 10.1182/blood-2002-07-2290. Epub 2003 Jan 23.

Abstract

We describe herein a case of nephrotic syndrome (NS) following allogeneic bone marrow transplantation (allo-BMT) for natural killer cell leukemia/lymphoma. Histologic studies defined the diagnosis as crescentic glomerulonephritis with massive immunoglobulin A (IgA) deposition, which has never been reported in NS cases following allo-BMT. Most of the massive infiltrated cells in the interstice were CD3(+)CD4(-)CD8(+) T cells derived from the donor. We observed mesangial deposition of Haemophilus parainfluenza outer membrane (OMHP) antigen and decreased glycosylation of the IgA1 hinge in the recipient's samples is consistent with the recently reported pathogenesis of IgA nephropathy. Further, the titer of IgA antibody against the donor serum was as high as other IgA nephropathy cases. These findings suggest that NS and crescentic glomerulonephritis in this case occurred as one of the forms of chronic graft-versus-host disease (GVHD), and that IgA deposition was associated with H parainfluenza and decreased glycosylation of the IgA1 hinge.

摘要

我们在此描述了一例因自然杀伤细胞白血病/淋巴瘤接受异基因骨髓移植(allo - BMT)后发生肾病综合征(NS)的病例。组织学研究将诊断确定为伴有大量免疫球蛋白A(IgA)沉积的新月体性肾小球肾炎,这种情况在allo - BMT后的NS病例中从未有过报道。间质中大多数大量浸润细胞是来自供体的CD3(+)CD4(-)CD8(+) T细胞。我们在受体样本中观察到副流感嗜血杆菌外膜(OMHP)抗原的系膜沉积以及IgA1铰链区糖基化减少,这与最近报道的IgA肾病发病机制一致。此外,针对供体血清的IgA抗体滴度与其他IgA肾病病例一样高。这些发现表明,该病例中的NS和新月体性肾小球肾炎是作为慢性移植物抗宿主病(GVHD)的一种形式发生的,并且IgA沉积与副流感嗜血杆菌以及IgA1铰链区糖基化减少有关。

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