Complex congenital isolated hemihyperplasia

Authors

  • Fernanda de Arruda Steffen FCMS/PUC-SP
  • Guilherme Lippi Ciantelli FCMS/PUC-SP
  • Lívea Athayde de Morais FCMS/PUC-SP
  • Marília Akemi Uzuelle Takahashi FCMS/PUC-SP
  • Christiane Saiury Lopes Inoue FCMS/PUC-SP
  • Sâmela Ester Rosique FCMS/PUC-SP
  • Marta Wey Vieira FCMS/PUC-SP

Keywords:

hyperplasia, Beckwith-Wiedemann Syndrome, Wilms tumor.

Abstract

ABSTRACT
Isolated Hemihyperplasia has a prevalence of 1:86,000 births and consists in a one or more body part's asymmetry, in a greater extent than could be attributed to a variation of normality, with unknown etiology. The authors describe in this article another case of this rare abnormality.

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Author Biographies

Fernanda de Arruda Steffen, FCMS/PUC-SP

Acadêmica do curso de Medicina FCMS/PUC-SP

Guilherme Lippi Ciantelli, FCMS/PUC-SP

Acadêmico do curso de Medicina FCMS/PUC-SP

Lívea Athayde de Morais, FCMS/PUC-SP

Acadêmica do curso de Medicina FCMS/PUC-SP

Marília Akemi Uzuelle Takahashi, FCMS/PUC-SP

Acadêmica do curso de Medicina FCMS/PUC-SP

Christiane Saiury Lopes Inoue, FCMS/PUC-SP

Acadêmica do curso de Medicina FCMS/PUC-SP

Sâmela Ester Rosique, FCMS/PUC-SP

Acadêmica do curso de Medicina FCMS/PUC-SP

Marta Wey Vieira, FCMS/PUC-SP

Professora do Depto. de Medicina FCMS/PUC-SP

References

Hemihyperplasia, isolated; IH. In: OMIM Online Mendelian Inheritance in Man [Internet]. Baltimore: Johns Hopkins University; c1966-2011 [acesso em 12 set. 2011]. Disponível em: http://omim.org/entry/235000?search=idiopatic%20hemihypertrophy&highlight=hemihypertrophy%20idiopatic.

Gomes MVM, Ramos ES. Beck-Wiedmann Syndrome and isolated hemihyperplasia. Rev Paul Med. 2003;121(3):133-8.

Ballock MDT, Georgia L, Wiesner MD, Myers MT, Thompson GH, Cleveland O. Hemihypertrophy, J Bone Joint Surg. 1997;79(11):1731-8.

Maniar S, Azzi K, Iragi H, El Hassan GM, Chraibi A, Gaouzi A. Idiopatic corporeal hemihypertrophy associated with hemypertrichosis. Ann Endocrinol. 2001; 72(1):48-52.

Teixeira RAP, Bruniera P, Sredni ST, Próspero JD. Tumor de Wilms: avaliação clínica, histológica, imunoistoquímica (p53) e prognóstico. Pediatria. 2001;23(2):137-45.

Niemitz EL, Feinberg AP, Brandenburg SA, Grundy PE, DeBaun MR. Children with idiopathic hemihypertrophy and Beckwith-Wiedemann Syndrome have different constitutional epigenotypes associated with Wilms Tumor. Am J Hum Genet. 2005;77:887-91.

Zuniga SR, Zavala AB, Pérez CL. Hemihipertrofia congénita. Rev Chil Pediatr. 1985;56(2):87-91.

Clericuzio CL, Martin RA. Diagnostic criteria and tumor screening for individuals with isolated hemihyperplasia. Genet Med. 2009;11(3):220-2.

Clauser L, Tieghi R, Polito J. Treatment of macroglossia in Beckwith-Wiedemann syndrome. J Craniofac Surg. 2006;17(2):369-72.

D'Agostino L, Costa CSSA. Síndrome de Beckwith-Wiedmann. In: Rocha LD, Zanini SA, Thomé R, Mélega JM, organizadores. Cirurgia plástica: fundamentos e arte: cirurgia reparadora de cabeça e pescoço. Rio de Janeiro: Medsi; 2002. p.530-8.

Chen CP. Syndromes and disorders associated with omphalocele (I): Beckwith-Wiedemann syndrome. Taiwan J Obstet Gynecol. 2007;46(2):96-102.

Rocha FMKU, Digiovanni M, Pascolat G, Ribas MM. Hemihipertrofia Isolada: relato de caso. J Parana Pediatr. 2005;10(8):32-5.

Rodrigues KE, Camargo B. Diagnóstico precoce do câncer infantil: responsabilidade de todos. Rev Assoc Méd Bras. 2003;49(1):29-34.

Published

2013-06-28

How to Cite

Steffen, F. de A., Ciantelli, G. L., Morais, L. A. de, Takahashi, M. A. U., Inoue, C. S. L., Rosique, S. E., & Vieira, M. W. (2013). Complex congenital isolated hemihyperplasia. Revista Da Faculdade De Ciências Médicas De Sorocaba, 15(2), 24–27. Retrieved from https://revistas.pucsp.br/index.php/RFCMS/article/view/7924

Issue

Section

Case Report