Skip to main content
Top
Published in: Clinical and Experimental Nephrology 2/2012

01-04-2012 | Case Report

Oligomeganephronia in an adult without end stage renal failure

Authors: Yoshinobu Fuke, Seiichiro Hemmi, Mamiko Kajiwara, Minako Yabuki, Takayuki Fujita, Masayoshi Soma

Published in: Clinical and Experimental Nephrology | Issue 2/2012

Login to get access

Abstract

A 23 year-old male was investigated for hypertension, moderate renal insufficiency, persistent proteinuria and bilateral small kidneys. The renal pathological features were diagnostic with greatly enlarged glomeruli (the mean diameter was 325 μm, which was approximately two times larger than normal glomeruli), indicating oligomeganephronia (OMN). He also showed malrotated kidneys, expanded extrarenal pelvis, and hearing loss. Thus, these clinical and pathological features aided in diagnosing the renal disorder as OMN. This is a very rare case of OMN, which did not advance to end-stage renal failure as an adult. We believe that multiple anomalies might be suggestive findings of OMN in patients, such as renal insufficiency, persistent proteinuria, and bilateral small kidneys.
Literature
1.
go back to reference Habib R, Courtecuisse V, athieum H, Royer P. A peculiar anatomo-clinical type of chronic renal insufficiency in the child: bilateral congenital oligonephronic hypoplasia. J Urol Nephrol (Paris). 1962;68:139–43. Habib R, Courtecuisse V, athieum H, Royer P. A peculiar anatomo-clinical type of chronic renal insufficiency in the child: bilateral congenital oligonephronic hypoplasia. J Urol Nephrol (Paris). 1962;68:139–43.
2.
go back to reference Broyer M, Soto B, Gagnadoux MF, Adi M, Rica C, Gubler MC. Oligomeganephronic renal hypoplasia. Adv Nephrol Necker Hosp. 1997;26:47–63.PubMed Broyer M, Soto B, Gagnadoux MF, Adi M, Rica C, Gubler MC. Oligomeganephronic renal hypoplasia. Adv Nephrol Necker Hosp. 1997;26:47–63.PubMed
3.
go back to reference Drukker A. Oligonephropathy: from a rare childhood disorder to a possible health problem in the adult. Isr Med Assoc J. 2002;4(3):191–5.PubMed Drukker A. Oligonephropathy: from a rare childhood disorder to a possible health problem in the adult. Isr Med Assoc J. 2002;4(3):191–5.PubMed
4.
go back to reference Royer P, Habib R, Courtecuisse V, Leclerc F. Bilateral renal hypoplasia with oligonephronia. (Study of 21 cases). Arch Fr Pediatr. 1967;24(3):249–68.PubMed Royer P, Habib R, Courtecuisse V, Leclerc F. Bilateral renal hypoplasia with oligonephronia. (Study of 21 cases). Arch Fr Pediatr. 1967;24(3):249–68.PubMed
5.
go back to reference Tsuboi N, Kawamura T, Koike K, Okonogi H, Hirano K, Hamaguchi A, Miyazaki Y, Ogura M, Joh K, Utsunomiya Y, Hosoya T. Glomerular density in renal biopsy specimens predicts the long-term prognosis of IgA nephropathy. Clin J Am Soc Nephrol. 2010;5(1):39–44.PubMedCrossRef Tsuboi N, Kawamura T, Koike K, Okonogi H, Hirano K, Hamaguchi A, Miyazaki Y, Ogura M, Joh K, Utsunomiya Y, Hosoya T. Glomerular density in renal biopsy specimens predicts the long-term prognosis of IgA nephropathy. Clin J Am Soc Nephrol. 2010;5(1):39–44.PubMedCrossRef
6.
go back to reference Salomon R, Tellier AL, Attie-Bitach T, Amiel J, Vekemans M, Lyonnet S, Dureau P, Niaudet P, Gubler MC, Broyer M. PAX2 mutations in oligomeganephronia. Kidney Int. 2001;59(2):457–62.PubMedCrossRef Salomon R, Tellier AL, Attie-Bitach T, Amiel J, Vekemans M, Lyonnet S, Dureau P, Niaudet P, Gubler MC, Broyer M. PAX2 mutations in oligomeganephronia. Kidney Int. 2001;59(2):457–62.PubMedCrossRef
7.
go back to reference Park SH, Chi JG. Oligomeganephronia associated with 4p deletion type chromosomal anomaly. Pediatr Pathol. 1993;13(6):731–40.PubMedCrossRef Park SH, Chi JG. Oligomeganephronia associated with 4p deletion type chromosomal anomaly. Pediatr Pathol. 1993;13(6):731–40.PubMedCrossRef
8.
go back to reference Anderson CE, Wallerstein R, Zamerowski ST, Witzleben C, Hoyer JR, Gibas L, Jackson LG. Ring chromosome 4 mosaicism coincidence of oligomeganephronia and signs of Seckel syndrome. Am J Med Genet. 1997;72(3):281–5.PubMedCrossRef Anderson CE, Wallerstein R, Zamerowski ST, Witzleben C, Hoyer JR, Gibas L, Jackson LG. Ring chromosome 4 mosaicism coincidence of oligomeganephronia and signs of Seckel syndrome. Am J Med Genet. 1997;72(3):281–5.PubMedCrossRef
9.
go back to reference Hirooka M, Kubota N, Ohno T. Congenital nephropathy associated with hearing loss, ocular abnormalities, mental retardation, convulsions and abnormal E.E.G. Tohoku J Exp Med. 1969;98:329–43.PubMedCrossRef Hirooka M, Kubota N, Ohno T. Congenital nephropathy associated with hearing loss, ocular abnormalities, mental retardation, convulsions and abnormal E.E.G. Tohoku J Exp Med. 1969;98:329–43.PubMedCrossRef
10.
go back to reference Yui I, Awazu M, Takeuchi Y, Fukuda J, Hanada T, Sakaguchi H. Oligomeganephronia with multiple anomalies. Nippon Jinzo Gakkai Shi. 1984;26(11):1529–37.PubMed Yui I, Awazu M, Takeuchi Y, Fukuda J, Hanada T, Sakaguchi H. Oligomeganephronia with multiple anomalies. Nippon Jinzo Gakkai Shi. 1984;26(11):1529–37.PubMed
11.
go back to reference Kawanishi K, Takei T, Kojima C, Moriyama T, Sugiura H, Itabashi M, Tsukada M, Uchida K, Honda K, Nitta K. Three cases of late-onset oligomeganephronia. Nephrol Dial Transpl Plus. 2011;4:14–6.CrossRef Kawanishi K, Takei T, Kojima C, Moriyama T, Sugiura H, Itabashi M, Tsukada M, Uchida K, Honda K, Nitta K. Three cases of late-onset oligomeganephronia. Nephrol Dial Transpl Plus. 2011;4:14–6.CrossRef
12.
go back to reference McGraw M, Poucell S, Sweet J, Baumal R. The significance of focal segmental glomerulosclerosis in oligomeganephronia. Int J Pediatr Nephrol. 1984;5(2):67–72.PubMed McGraw M, Poucell S, Sweet J, Baumal R. The significance of focal segmental glomerulosclerosis in oligomeganephronia. Int J Pediatr Nephrol. 1984;5(2):67–72.PubMed
Metadata
Title
Oligomeganephronia in an adult without end stage renal failure
Authors
Yoshinobu Fuke
Seiichiro Hemmi
Mamiko Kajiwara
Minako Yabuki
Takayuki Fujita
Masayoshi Soma
Publication date
01-04-2012
Publisher
Springer Japan
Published in
Clinical and Experimental Nephrology / Issue 2/2012
Print ISSN: 1342-1751
Electronic ISSN: 1437-7799
DOI
https://doi.org/10.1007/s10157-011-0560-8

Other articles of this Issue 2/2012

Clinical and Experimental Nephrology 2/2012 Go to the issue
Live Webinar | 27-06-2024 | 18:00 (CEST)

Keynote webinar | Spotlight on medication adherence

Live: Thursday 27th June 2024, 18:00-19:30 (CEST)

WHO estimates that half of all patients worldwide are non-adherent to their prescribed medication. The consequences of poor adherence can be catastrophic, on both the individual and population level.

Join our expert panel to discover why you need to understand the drivers of non-adherence in your patients, and how you can optimize medication adherence in your clinics to drastically improve patient outcomes.

Prof. Kevin Dolgin
Prof. Florian Limbourg
Prof. Anoop Chauhan
Developed by: Springer Medicine
Obesity Clinical Trial Summary

At a glance: The STEP trials

A round-up of the STEP phase 3 clinical trials evaluating semaglutide for weight loss in people with overweight or obesity.

Developed by: Springer Medicine

Highlights from the ACC 2024 Congress

Year in Review: Pediatric cardiology

Watch Dr. Anne Marie Valente present the last year's highlights in pediatric and congenital heart disease in the official ACC.24 Year in Review session.

Year in Review: Pulmonary vascular disease

The last year's highlights in pulmonary vascular disease are presented by Dr. Jane Leopold in this official video from ACC.24.

Year in Review: Valvular heart disease

Watch Prof. William Zoghbi present the last year's highlights in valvular heart disease from the official ACC.24 Year in Review session.

Year in Review: Heart failure and cardiomyopathies

Watch this official video from ACC.24. Dr. Biykem Bozkurt discusses last year's major advances in heart failure and cardiomyopathies.