Abstract
Hemihypertrophy (Hemihyperplasia) is characterized by asymmetric overgrowth of cranium, face, trunk, limbs and digits. It may be an isolated form or it may occur in several syndromes. In both syndromic and isolated hemihypertrophy there are an increased risk of embryonal tumors, most commonly Wilms tumor, although other abdominal tumors such as hepatoblastoma and adrenal cell carcinoma also ocur. Consequently, along with the literature, we present a case of patient with Isolated Hemihypertrophy.
References
- Bliek J, Maas S, Alders M, Merks JHM, Mannens M. Epigenotype, phenotype, and tumors in patients with isolated hemihyperplasia. J Pediatr 2008;153:95–100.
- Balamtekin N, Öztürk A. Presentation Of A Child With Isolated Hemihypertrophy And Rewiev Of The Literature. Erciyes Medical Journal 2006;28:44-46.
- Dempsey-Robertson M, Wilkes D, Stall A, Bush P. Incidence of abdominal tumors in syndromic and idiopathic hemihypertrophy/ isolated hemihyperplasia. J Pediatr Orthop 2012;32:322-326.
- Hoyme HE, Seaver LH, Jones KL, Procopio F, Crooks W, Feingold M. Isolated Hemihyperplasia (Hemihypertrophy): Report of a Prospective Multicenter Study of the Incidence of Neoplasia and Review. Am J Med Genet 1998;79:274-278.
- Zarate YA, Mena R, Martin LJ, Steele P, Tinkle BT, Hopkin RJ. Experience with hemihyperplasia and Beckwith-Wiedemann syndrome surveillance protocol. Am J Med Genet A 2009;149:1691-1697.
- Tan TY, Amor DJ. Tumour surveillance in Beckwith-Wiedemann syndrome and hemihyperplasia: A critical review of the evidence and suggested guidelines for local practice. J Paediatr Child Health 2006;42:486–490.
Abstract
Hemihipertrofi (hemihiperplazi) kranium, yüz, gövde, ekstremite ve parmakların asimetrik büyümesi ile karakterizedir. İzole olabileceği gibi bazı sendromlarda görülebilmektedir. Hem sendromik hem de izole hemihipertrofide Willms tümörü, hepatoblastom ve adrenal hücre karsinomu gibi embroyonel ve abdominal tümörlerin görülme sıklığı artmıştır. Bizde bu açıdan izole hemihipertrofili olguyu literatür eşliğinde sunuyoruz.
References
- Bliek J, Maas S, Alders M, Merks JHM, Mannens M. Epigenotype, phenotype, and tumors in patients with isolated hemihyperplasia. J Pediatr 2008;153:95–100.
- Balamtekin N, Öztürk A. Presentation Of A Child With Isolated Hemihypertrophy And Rewiev Of The Literature. Erciyes Medical Journal 2006;28:44-46.
- Dempsey-Robertson M, Wilkes D, Stall A, Bush P. Incidence of abdominal tumors in syndromic and idiopathic hemihypertrophy/ isolated hemihyperplasia. J Pediatr Orthop 2012;32:322-326.
- Hoyme HE, Seaver LH, Jones KL, Procopio F, Crooks W, Feingold M. Isolated Hemihyperplasia (Hemihypertrophy): Report of a Prospective Multicenter Study of the Incidence of Neoplasia and Review. Am J Med Genet 1998;79:274-278.
- Zarate YA, Mena R, Martin LJ, Steele P, Tinkle BT, Hopkin RJ. Experience with hemihyperplasia and Beckwith-Wiedemann syndrome surveillance protocol. Am J Med Genet A 2009;149:1691-1697.
- Tan TY, Amor DJ. Tumour surveillance in Beckwith-Wiedemann syndrome and hemihyperplasia: A critical review of the evidence and suggested guidelines for local practice. J Paediatr Child Health 2006;42:486–490.
Details
| Primary Language | Turkish |
|---|---|
| Journal Section | Articles |
| Authors | |
| Publication Date | December 1, 2013 |
| Submission Date | September 7, 2015 |
| Published in Issue | Year 2013 Volume: 3 Issue: 4 |
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