Skip to main content
Top
Published in: Pediatric Nephrology 9/2010

01-09-2010 | Brief Report

Renal agenesis in a child with ipsilateral hemihypertrophy

Authors: Nisa Cem Ören, Sebahattin Vurucu, Bülent Karaman, Fatih Örs

Published in: Pediatric Nephrology | Issue 9/2010

Login to get access

Abstract

Hemihypertrophy is a clinical condition defined as an asymmetric enlargement of one side of the body. Inguinal hernias, renal cysts, cryptorchidism, ectasias of collecting tubes, medullary sponge kidney and horse-shoe kidney are examples of abnormalities associated with hemihypertrophy that have been described in the literature. We report here a 17.2-year-old patient with a left hemihypertrophy and renal agenesis with contralateral right compensatory renal hypertrophy together with normal renal function and blood pressure in the absence of proteinuria. He also presented with faint macular hyperpigmented skin lesions on his left upper arm, forehead and abdomen. To the best of our knowledge, this is the first report of renal agenesis and hemihypertrophy in the same patient. Hemihypertrophy can be seen as a component of Klippel–Trenaunay–Weber syndrome. The other components of this syndrome are varicose veins, skin naevus and arteriovenous malformations. Although renal agenesis, hemihypertrophy and hyperpigmented macular skin lesions (skin naevuses) may be incidental findings, together they may form a variant of Klippel–Trenaunay–Weber syndrome, as in our case.
Literature
1.
go back to reference Tomkooya Y (1988) Congenital hemihypertrophy and medullary sponge kidney. Br J Radiol 61:851–853CrossRef Tomkooya Y (1988) Congenital hemihypertrophy and medullary sponge kidney. Br J Radiol 61:851–853CrossRef
2.
go back to reference Cohen MM Jr (1989) A comprehensive and critical assessment of overgrowth and overgrowth syndromes. Adv Hum Genet 18:373–376 Cohen MM Jr (1989) A comprehensive and critical assessment of overgrowth and overgrowth syndromes. Adv Hum Genet 18:373–376
3.
go back to reference Scott RH, Walker L, Olsen ØE, Levitt G, Kenney I, Maher E, Owens CM, Pritchard-Jones K, Craft A, Rahman N (2006) Surveillance for Wilms tumour in at-risk children: pragmatic recommendations for best practice. Arch Dis Child 91:995–999CrossRefPubMed Scott RH, Walker L, Olsen ØE, Levitt G, Kenney I, Maher E, Owens CM, Pritchard-Jones K, Craft A, Rahman N (2006) Surveillance for Wilms tumour in at-risk children: pragmatic recommendations for best practice. Arch Dis Child 91:995–999CrossRefPubMed
4.
go back to reference Klippel M, Trenaunay P (1900) Du noevus variquex osteo-hypertrophique. Arch Gen Med (Paris) 185:641–672 Klippel M, Trenaunay P (1900) Du noevus variquex osteo-hypertrophique. Arch Gen Med (Paris) 185:641–672
5.
go back to reference Weber FP (1907) Angioma formation in connection with hypertrophy of limbs and hemihypertrophy. Br J Dermatol 19:231–235 Weber FP (1907) Angioma formation in connection with hypertrophy of limbs and hemihypertrophy. Br J Dermatol 19:231–235
6.
go back to reference Kanterman RY, Witt PD, Hsieh PS, Picus D (1996) Klippel-Trenaunay Syndrome: imaging findings and percutaneous intervention. AJR Am J Roentgenol 167:989–995PubMed Kanterman RY, Witt PD, Hsieh PS, Picus D (1996) Klippel-Trenaunay Syndrome: imaging findings and percutaneous intervention. AJR Am J Roentgenol 167:989–995PubMed
7.
go back to reference Pappas AM, Nehme AM (1979) Leg length discrepancy associated with hypertrophy. Clin Orthop Relat Res 144:198–211PubMed Pappas AM, Nehme AM (1979) Leg length discrepancy associated with hypertrophy. Clin Orthop Relat Res 144:198–211PubMed
8.
go back to reference Anderson M, Messner MB, Green WT (1964) Distribution of lengths of the normal femur and tibia in children from one to eighteen years of age. J Bone Joint Surg Am 46:1197–1202PubMed Anderson M, Messner MB, Green WT (1964) Distribution of lengths of the normal femur and tibia in children from one to eighteen years of age. J Bone Joint Surg Am 46:1197–1202PubMed
9.
go back to reference Rush WA, Steiner HA (1946) A study of lower extremity length inequality. Am J Roentgenol Radium Ther 56:616–623PubMed Rush WA, Steiner HA (1946) A study of lower extremity length inequality. Am J Roentgenol Radium Ther 56:616–623PubMed
10.
go back to reference Ringrose RE, Jabbour JT, Keele DK (1965) Hemihypertrophy. Pediatrics 36:434–448PubMed Ringrose RE, Jabbour JT, Keele DK (1965) Hemihypertrophy. Pediatrics 36:434–448PubMed
11.
go back to reference Ballock RT, Wiesner GL, Myers MT, Thompson GH (1997) Hemihypertrophy. Concepts and controversies. J Bone Joint Surg Am 79:1731–1738PubMed Ballock RT, Wiesner GL, Myers MT, Thompson GH (1997) Hemihypertrophy. Concepts and controversies. J Bone Joint Surg Am 79:1731–1738PubMed
12.
go back to reference Beckwith JB (1963) Extreme cytomegaly of adrenal fetal cortex, omphalocele, hyperplasia of kidneys and pancreas and Leydig cell hyperplasia: another syndrome? Presented at the Annual Meeting of the Western Society for Pediatrics Research, Los Angeles Beckwith JB (1963) Extreme cytomegaly of adrenal fetal cortex, omphalocele, hyperplasia of kidneys and pancreas and Leydig cell hyperplasia: another syndrome? Presented at the Annual Meeting of the Western Society for Pediatrics Research, Los Angeles
13.
go back to reference Wiedemann HR (1964) Complexe malformatif familial avec hernie ombilicale et macroglossie: un “syndrome nouveau”? J Genet Hum 13:223–232PubMed Wiedemann HR (1964) Complexe malformatif familial avec hernie ombilicale et macroglossie: un “syndrome nouveau”? J Genet Hum 13:223–232PubMed
14.
15.
go back to reference Cohen MM Jr, Hayden PW (1979) A newly recognized hamartomatous syndrome. Birth Defects Orig Arctic Ser 15:291–296 Cohen MM Jr, Hayden PW (1979) A newly recognized hamartomatous syndrome. Birth Defects Orig Arctic Ser 15:291–296
17.
go back to reference Wollmann HA, Kirchner T, Enders H, Preece MA, Ranke MB (1995) Growth and symptoms in Silver–Russell Syndrome: review on the basis of 386 patients. Eur J Pediatr 154:958–968CrossRefPubMed Wollmann HA, Kirchner T, Enders H, Preece MA, Ranke MB (1995) Growth and symptoms in Silver–Russell Syndrome: review on the basis of 386 patients. Eur J Pediatr 154:958–968CrossRefPubMed
18.
go back to reference Price SM, Stanhope R, Garrett C, Preece MA, Trembath RC (1999) The spectrum of Silver-Russell syndrome: a clinical and molecular genetic study and new diagnostic criteria. J Med Genet 36:837–842PubMed Price SM, Stanhope R, Garrett C, Preece MA, Trembath RC (1999) The spectrum of Silver-Russell syndrome: a clinical and molecular genetic study and new diagnostic criteria. J Med Genet 36:837–842PubMed
19.
go back to reference Rossignol S, Netchine I, Le Bouc Y, Gicquel C (2008) Epigenetics in Silver–Russell syndrome. Best Pract Res Clin Endocrinol Metab 22:403–414CrossRefPubMed Rossignol S, Netchine I, Le Bouc Y, Gicquel C (2008) Epigenetics in Silver–Russell syndrome. Best Pract Res Clin Endocrinol Metab 22:403–414CrossRefPubMed
20.
go back to reference Gucev ZS, Tasic V, Jancevska A, Kirovski I (2009) Silver–Russell syndrome (SRS): multiple pituitary hormone deficiency, lack of H19 hypomethylation and favourable growth hormone (GH) treatment response. J Genet 88:239–243CrossRefPubMed Gucev ZS, Tasic V, Jancevska A, Kirovski I (2009) Silver–Russell syndrome (SRS): multiple pituitary hormone deficiency, lack of H19 hypomethylation and favourable growth hormone (GH) treatment response. J Genet 88:239–243CrossRefPubMed
21.
go back to reference Clericuzio CL, Johnson C (1995) Screening for Wilms tumor in high-risk individuals. Hematol Oncol Clin North Am 9:1253–1265PubMed Clericuzio CL, Johnson C (1995) Screening for Wilms tumor in high-risk individuals. Hematol Oncol Clin North Am 9:1253–1265PubMed
Metadata
Title
Renal agenesis in a child with ipsilateral hemihypertrophy
Authors
Nisa Cem Ören
Sebahattin Vurucu
Bülent Karaman
Fatih Örs
Publication date
01-09-2010
Publisher
Springer-Verlag
Published in
Pediatric Nephrology / Issue 9/2010
Print ISSN: 0931-041X
Electronic ISSN: 1432-198X
DOI
https://doi.org/10.1007/s00467-010-1525-y

Other articles of this Issue 9/2010

Pediatric Nephrology 9/2010 Go to the issue