Literature DB >> 3594937

The glomerular tip lesion: a steroid responsive nephrotic syndrome.

M Beaman, A J Howie, J Hardwicke, J Michael, D Adu.   

Abstract

The glomerular tip nephropathy is a cause of the nephrotic syndrome and has distinct pathological features. Glomerular tufts appear normal on light microscopy except for a segmental lesion invariably present in all glomeruli at the origin of the proximal tubule. Data on twenty adults whose renal biopsies demonstrated this lesion and who were followed for a mean of 7.4 years are analyzed. Eighteen patients were treated with steroids; ten of these had complete remission of proteinuria and seven a significant reduction of their proteinuria. Ten patients had moderately impaired renal function (serum creatinine greater than 120 mumol/l) at presentation, eight received steroids and achieved a reduction in serum creatinine. The prognosis was good, with no patient developing chronic renal failure requiring dialysis.

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Year:  1987        PMID: 3594937

Source DB:  PubMed          Journal:  Clin Nephrol        ISSN: 0301-0430            Impact factor:   0.975


  4 in total

Review 1.  Segmental sclerosing glomerular lesions.

Authors:  A J Howie
Journal:  Pediatr Nephrol       Date:  1993-08       Impact factor: 3.714

2.  Glomerular tip changes in childhood minimal change nephropathy.

Authors:  Alexander J Howie; Anju Agarwal; Neil J Sebire; Richard S Trompeter
Journal:  Pediatr Nephrol       Date:  2008-04-30       Impact factor: 3.714

3.  Urinary IL-6: a marker for mesangial proliferative glomerulonephritis?

Authors:  C Gordon; N Richards; A J Howie; K Richardson; J Michael; D Adu; P Emery
Journal:  Clin Exp Immunol       Date:  1991-10       Impact factor: 4.330

Review 4.  Practical Application of Columbia Classification for Focal Segmental Glomerulosclerosis.

Authors:  Man-Hoon Han; Yong-Jin Kim
Journal:  Biomed Res Int       Date:  2016-05-09       Impact factor: 3.411

  4 in total

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