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伯杰氏病(IgA肾病)的活动期和慢性期。

Active and chronic phases of Berger's disease (IgA nephropathy).

作者信息

Feltis J T, Churg J, Holley K M, Feiner H, Gallo G, Ackad A S

出版信息

Am J Kidney Dis. 1984 Mar;3(5):349-56. doi: 10.1016/s0272-6386(84)80082-7.

DOI:10.1016/s0272-6386(84)80082-7
PMID:6367440
Abstract

Berger's disease, or IgA nephropathy, is generally considered as pursuing a chronic course, often with recurrent attacks of gross hematuria or persistent microscopic hematuria. However, little attention has been paid to the acute changes that may accompany this nephropathy, and there are few reports of follow-up renal biopsy studies in these patients. We have had the opportunity to study two patients with Berger's disease (IgA nephropathy) in whom initial and follow-up renal biopsy studies were available. Both of these patients presented clinically with gross hematuria and moderately heavy proteinuria. In both cases, the initial renal biopsy disclosed diffuse mesangial proliferation associated with crescent formation, while follow-up biopsy disclosed only mild mesangial proliferation and no crescents. In one case electron microscopy revealed prominent subendothelial and small mesangial deposits in the initial biopsy, which became almost solely large mesangial in the second biopsy. The other case demonstrated only mesangial deposits in both biopsies.

摘要

伯杰氏病,即IgA肾病,通常被认为病程呈慢性,常伴有肉眼血尿反复发作或持续性镜下血尿。然而,对于这种肾病可能伴随的急性变化关注甚少,关于这些患者的随访肾活检研究报告也很少。我们有机会研究两名患有伯杰氏病(IgA肾病)的患者,他们有初始和随访肾活检研究资料。这两名患者临床上均表现为肉眼血尿和中度蛋白尿。在这两个病例中,初始肾活检显示弥漫性系膜增生伴新月体形成,而随访活检仅显示轻度系膜增生且无新月体。在一个病例中,电子显微镜检查显示初始活检中有明显的内皮下和小系膜沉积物,而在第二次活检中几乎仅为大系膜沉积物。另一例在两次活检中均仅显示系膜沉积物。

相似文献

1
Active and chronic phases of Berger's disease (IgA nephropathy).伯杰氏病(IgA肾病)的活动期和慢性期。
Am J Kidney Dis. 1984 Mar;3(5):349-56. doi: 10.1016/s0272-6386(84)80082-7.
2
Idiopathic recurrent macroscopic hematuria and mesangial IgA-IgG deposits in children (Berger's disease).儿童特发性复发性肉眼血尿和系膜IgA-IgG沉积(伯杰氏病)
Clin Nephrol. 1972 Mar-Apr;1(2):63-9.
3
[IgA nephropathy (Berger's disease) in children].[儿童IgA肾病(伯杰氏病)]
Bol Med Hosp Infant Mex. 1992 Dec;49(12):832-8.
4
Long-standing spontaneous clinical remission and glomerular improvement in primary IgA nephropathy (Berger's disease).
Am J Nephrol. 1987;7(6):440-4. doi: 10.1159/000167516.
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IgA glomerulonephritis. Mesangial IgA deposition without systemic signs (Berger's disease).IgA 肾小球肾炎。系膜 IgA 沉积,无全身症状(伯杰氏病)。
Int Urol Nephrol. 1979;11(4):367-75. doi: 10.1007/BF02086824.
6
[Primary nephropathy due to mesangial deposits of IgA (Berger's disease)].IgA系膜沉积所致原发性肾病(伯杰氏病)
Rev Med Chil. 1990 Feb;118(2):125-33.
7
ANCA-associated crescentic glomerulonephritis with mesangial IgA deposits.伴有系膜IgA沉积的抗中性粒细胞胞浆抗体相关性新月体性肾小球肾炎
Am J Kidney Dis. 2000 Oct;36(4):709-18. doi: 10.1053/ajkd.2000.17615.
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[Berger's disease or the disease of recurrent macroscopic hematuria or the disease with mesangial deposits of IgA-IgG].[伯杰氏病或复发性肉眼血尿病或伴有IgA-IgG系膜沉积物的疾病]
Minerva Pediatr. 1978 Nov 30;30(22):1817-9.
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Mesangial deposition of J chain-linked polymeric IgA in IgA nephropathy.IgA肾病中J链连接的聚合IgA的系膜沉积。
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10
Ultrastructure of acute glomerular injury in IgA nephritis.
Arch Pathol Lab Med. 1980 Jun;104(6):303-7.

引用本文的文献

1
Reversal of active glomerular lesions after immunosuppressive therapy in patients with IgA nephropathy: a repeat-biopsy based observation.IgA肾病患者免疫抑制治疗后活动性肾小球病变的逆转:一项基于重复活检的观察
J Nephrol. 2015 Aug;28(4):441-9. doi: 10.1007/s40620-014-0165-x. Epub 2015 Jan 14.
2
Do genetic factors play a role in Berger's disease?遗传因素在薄基底膜肾病中起作用吗?
Pediatr Nephrol. 1987 Jul;1(3):447-54. doi: 10.1007/BF00849253.
3
Course and long-term outcome of idiopathic IgA nephropathy in children.儿童特发性IgA肾病的病程及长期预后
Pediatr Nephrol. 1991 Jul;5(4):383-6. doi: 10.1007/BF01453658.