Literature DB >> 7959667

Insudative lesions--their pathogenesis and association with glomerular obsolescence in diabetes: a dynamic hypothesis based on single views of advancing human diabetic nephropathy.

L C Stout1, S Kumar, E B Whorton.   

Abstract

Kidneys from 74 consecutive, primarily non-insulin-dependent diabetics at autopsy and 59 age-, sex, and ethnic group-matched controls were examined qualitatively and semiquantitatively to determine the prevalence and severity of insudative lesions (ILs) and obsolescent glomeruli with (OGcFC) and without (OGsFC) insudative (fibrin cap) lesions. A subset of 25 cases with advanced diabetic changes was examined using serial sections, immunohistochemical stains, and electron microscopy to determine the pathogenesis of ILs and OGcFCs. Insudative lesions consisted of intramural accumulations (hereafter called deposits) of presumably imbibed plasma proteins and lipids within renal arterioles, glomerular capillaries, Bowman's capsule, and proximal convoluted tubules. Insudative lesions in Bowman's capsule are called capsular drop lesions (CDs), in glomerular capillaries they are called fibrin cap lesions (FC), and in afferent and efferent arterioles they are called hyalinized afferent (HA) and hyalinized efferent (HE) arterioles, respectively. All ILs were much more numerous and/or larger in diabetics than in controls. Contrary to previous opinion, CDs and HE arterioles were not specific for diabetes, being present in small numbers in nine (15%) controls. Controls with CD/HE arterioles had far more HA arterioles and focal mesangiolyses (FMs) than those without. Insudative lesions consisted of the well known homogenous eosinophilic deposits (homogenous eosinophilic ILs) and the less familiar foamy, reticulated, and vacuolar deposits (heterogenous lucent ILs). Homogenous eosinophilic ILs were predominant in afferent arterioles and more so in efferent arterioles, and were segregated into globules of varying density with the denser deposits located peripherally. Two types of CDs, which differed sharply in location and composition, were found. The first was mostly homogenous eosinophilic, usually without capsular adhesions and located near the vascular pole close to preglomerular arterioles. The second was mostly heterogenous lucent, located away from the vascular pole, and consistently connected by adhesions to the capillary tuft usually near FMs and/or Kimmelstiel-Wilson (KW) nodules. The latter ILs sometimes extended in continuity along the internal surface of the basement membrane from Bowman's capsule into the proximal convoluted tubule. It was hypothesized that ILs traveled centrifugally through the walls of preglomerular arterioles to form the first type of CD and longitudinally within the walls of afferent arterioles and glomerular capillaries and through adhesions to form the second. Contrary to previous opinion, FCs were consistently intramural. When numerous, FCs were associated with a form of glomerular obsolescence called OGcFC.(ABSTRACT TRUNCATED AT 400 WORDS)

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Year:  1994        PMID: 7959667     DOI: 10.1016/0046-8177(94)90039-6

Source DB:  PubMed          Journal:  Hum Pathol        ISSN: 0046-8177            Impact factor:   3.466


  11 in total

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2.  A case of idiopathic nodular glomerulosclerosis with fibrin caps.

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Journal:  Clin Exp Nephrol       Date:  2011-08-17       Impact factor: 2.801

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Review 4.  Renal endothelial dysfunction in diabetic nephropathy.

Authors:  Huifang Cheng; Raymond C Harris
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Journal:  Adv Chronic Kidney Dis       Date:  2018-03       Impact factor: 3.620

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Authors:  María José Soler; Marta Riera; Daniel Batlle
Journal:  Exp Diabetes Res       Date:  2012-02-08

7.  Paratubular basement membrane insudative lesions predict renal prognosis in patients with type 2 diabetes and biopsy-proven diabetic nephropathy.

Authors:  Koki Mise; Yutaka Yamaguchi; Junichi Hoshino; Toshiharu Ueno; Akinari Sekine; Keiichi Sumida; Masayuki Yamanouchi; Noriko Hayami; Tatsuya Suwabe; Rikako Hiramatsu; Eiko Hasegawa; Naoki Sawa; Takeshi Fujii; Shigeko Hara; Hitoshi Sugiyama; Hirofumi Makino; Jun Wada; Kenichi Ohashi; Kenmei Takaichi; Yoshifumi Ubara
Journal:  PLoS One       Date:  2017-08-15       Impact factor: 3.240

Review 8.  Molecular Mechanisms and Treatment Strategies in Diabetic Nephropathy: New Avenues for Calcium Dobesilate-Free Radical Scavenger and Growth Factor Inhibition.

Authors:  Hermann Haller; Linong Ji; Klaus Stahl; Anna Bertram; Jan Menne
Journal:  Biomed Res Int       Date:  2017-09-26       Impact factor: 3.411

9.  Diabetic condition induces hypertrophy and vacuolization in glomerular parietal epithelial cells.

Authors:  Takahisa Kawaguchi; Kazuhiro Hasegawa; Itaru Yasuda; Hirokazu Muraoka; Hiroyuki Umino; Hirobumi Tokuyama; Akinori Hashiguchi; Shu Wakino; Hiroshi Itoh
Journal:  Sci Rep       Date:  2021-01-15       Impact factor: 4.379

Review 10.  Histological changes of kidney in diabetic nephropathy.

Authors:  Mohsen Pourghasem; Hamid Shafi; Zahra Babazadeh
Journal:  Caspian J Intern Med       Date:  2015
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