Skip to main content

Advertisement

Log in

Renal agenesis in a child with ipsilateral hemihypertrophy

  • Brief Report
  • Published:
Pediatric Nephrology Aims and scope Submit manuscript

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.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3

References

  1. Tomkooya Y (1988) Congenital hemihypertrophy and medullary sponge kidney. Br J Radiol 61:851–853

    Article  Google Scholar 

  2. Cohen MM Jr (1989) A comprehensive and critical assessment of overgrowth and overgrowth syndromes. Adv Hum Genet 18:373–376

    Google Scholar 

  3. 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 91:995–999

    Article  CAS  PubMed  Google Scholar 

  4. Klippel M, Trenaunay P (1900) Du noevus variquex osteo-hypertrophique. Arch Gen Med (Paris) 185:641–672

    Google Scholar 

  5. Weber FP (1907) Angioma formation in connection with hypertrophy of limbs and hemihypertrophy. Br J Dermatol 19:231–235

    Google Scholar 

  6. Kanterman RY, Witt PD, Hsieh PS, Picus D (1996) Klippel-Trenaunay Syndrome: imaging findings and percutaneous intervention. AJR Am J Roentgenol 167:989–995

    CAS  PubMed  Google Scholar 

  7. Pappas AM, Nehme AM (1979) Leg length discrepancy associated with hypertrophy. Clin Orthop Relat Res 144:198–211

    PubMed  Google Scholar 

  8. 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 46:1197–1202

    CAS  PubMed  Google Scholar 

  9. Rush WA, Steiner HA (1946) A study of lower extremity length inequality. Am J Roentgenol Radium Ther 56:616–623

    CAS  PubMed  Google Scholar 

  10. Ringrose RE, Jabbour JT, Keele DK (1965) Hemihypertrophy. Pediatrics 36:434–448

    CAS  PubMed  Google Scholar 

  11. Ballock RT, Wiesner GL, Myers MT, Thompson GH (1997) Hemihypertrophy. Concepts and controversies. J Bone Joint Surg Am 79:1731–1738

    CAS  PubMed  Google Scholar 

  12. 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

    Google Scholar 

  13. Wiedemann HR (1964) Complexe malformatif familial avec hernie ombilicale et macroglossie: un “syndrome nouveau”? J Genet Hum 13:223–232

    CAS  PubMed  Google Scholar 

  14. O’Connor C, Levine D (2002) Case 49: Beckwith–Wiedemann Syndrome. Radiology 224:375–378

    Article  PubMed  Google Scholar 

  15. Cohen MM Jr, Hayden PW (1979) A newly recognized hamartomatous syndrome. Birth Defects Orig Arctic Ser 15:291–296

    Google Scholar 

  16. Demir MK (2008) Case 131: Proteus syndrome. Radiology 246:974–979

    Article  PubMed  Google Scholar 

  17. 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 154:958–968

    Article  CAS  PubMed  Google Scholar 

  18. 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 36:837–842

    CAS  PubMed  Google Scholar 

  19. Rossignol S, Netchine I, Le Bouc Y, Gicquel C (2008) Epigenetics in Silver–Russell syndrome. Best Pract Res Clin Endocrinol Metab 22:403–414

    Article  CAS  PubMed  Google Scholar 

  20. 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 88:239–243

    Article  CAS  PubMed  Google Scholar 

  21. Clericuzio CL, Johnson C (1995) Screening for Wilms tumor in high-risk individuals. Hematol Oncol Clin North Am 9:1253–1265

    CAS  PubMed  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Nisa Cem Ören.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Ören, N.C., Vurucu, S., Karaman, B. et al. Renal agenesis in a child with ipsilateral hemihypertrophy. Pediatr Nephrol 25, 1751–1754 (2010). https://doi.org/10.1007/s00467-010-1525-y

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00467-010-1525-y

Keywords

Navigation