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特发性小叶性肾小球肾炎(结节性系膜硬化):一种独特的诊断实体。

Idiopathic lobular glomerulonephritis (nodular mesangial sclerosis): a distinct diagnostic entity.

作者信息

Alpers C E, Biava C G

机构信息

Department of Pathology, University of Washington School of Medicine, Seattle.

出版信息

Clin Nephrol. 1989 Aug;32(2):68-74.

PMID:2766585
Abstract

Lobular glomerulonephritis is an entity first thought to have represented a primary disease of uncertain histogenesis, but more recently has generally been considered to represent a morphologic variant of membranoproliferative glomerulonephritis. We have encountered five patients who were found to have a lobular glomerulonephritis by renal biopsy, but in whom features of membranoproliferative glomerulonephritis types I, II, or III, could not be demonstrated and in whom alternate known diagnostic categories could be excluded. We suggest that lobular glomerulonephritis, or alternately, idiopathic nodular mesangial sclerosis, is an uncommon but persistent disease entity with a distinctive pathologic appearance and unknown pathogenesis.

摘要

小叶性肾小球肾炎最初被认为是一种组织发生不明的原发性疾病,但最近一般被认为是膜增生性肾小球肾炎的一种形态学变异。我们遇到了5例经肾活检发现患有小叶性肾小球肾炎的患者,但其中I型、II型或III型膜增生性肾小球肾炎的特征均未得到证实,且其他已知诊断类别也可排除。我们认为,小叶性肾小球肾炎,或者特发性结节性系膜硬化,是一种罕见但持续存在的疾病实体,具有独特的病理表现和未知的发病机制。

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