Anomalía de Peters. Presentação dum caso clínico
Palavras-chave:
defeito congênito, leucoma central, tratamentoResumo
Descreveu-se um caso com anomalia de Peters, defeito congênito da córnea que aparece de maneira geralmente esporádica e de etiología ainda incerta. Faz-se referência a suas formas de apresentação e aos possíveis tratamentos sendo o prognóstico mais sombrio quando se acompanha de manifestações sistémicas. Explicou-se como se chegou ao diagnóstico que é eminentemente clínico, deixando algumas considerações finais.
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Referências
1. Rezende RA, Uchoa UB, Uchoa R, Rapuano CJ, Laibson PR, Cohen EJ. Congenital corneal opacities in a cornea referral practice. Cornea. 2004; 23(6):565-70.
2. Harissi-Dagher M, Colby K. Anterior segment dysgenesis: Peters’ anomaly and sclerocornea. Int Ophthalmol Clin. 2008; 48(2):35-42. Review.
3. Bahn CF, Falls HF, Varley GA, Meyer RF, Edelhauser HF, Bourne WM. Classification of corneal endothelial disorders based on neural crest origin. Ophthalmology.1984; 91(6):558-63.
4. Maillette de Buy Wenniger-Prick LJ, Hennekam RC. The Peters’ plus syndrome: areview. Ann Genet. 2002; 45(2):97-103. Review.
5. Heon E, Barsoum-Homsy M, Cevrette L, Jacob JL, Milot J, Polemeno R, Musarella MA. Peters’ anomaly. The spectrum of associated ocular and systemic malfor-mations. Ophthalmic Paediatr Genet. 1992; 13(2):137-43.
6. Bhandari R, Ferri S, Whittaker B, Liu M, Lazzaro DR. Peters anomaly: review of the literature. Cornea. 2011; 30:939–44.
7. Eguía Martínez Frank et al. Manual de diagnóstico y tratamiento en Oftalmología. La Habana: ECIMED, 2009.
8. KanskyJJ.Oftalmología clínica VIed. España: Ed Elsevier,2006.
9. Ozeki H, Shirai S, Nozaki M, Sakurai E, Mizuno S, Ashikari M, Matsunaga N, Ogura Y: Ocular and systemic features of Peters anomaly. Graefes Arch Clin Exp Opthalmol 2000, 235:833-839.
10. MajanderAS,Lindahi PM,Vasara LK,Krootilla K.Anterior segment optical coherence tomography in congenital corneal opacities. Ophtalmology 2012; 119:2450-2457.
11. Nishide T,Nakanishi M,Hayakawa N,et al.Cataract surgery for tilted lens in Peters anomaly type 2.Case rep. Ophthalmol 2013;4:134- 7.
12. Lorry EA, Porco TC, Naseri A.Cost analysis of virtual – reality phacoemulsification in ophthalmology training programs. J Cataract Refract Surgery 2013; 39 1616- 7.
13. Nischal KK. A new appoach to the clasication of neonatal corneal opacities. Curr Opin Ophthalmol. 2012; 23:344-54.
14. Zaidman GW, Flanagan JK, Furey CC. Long-term visual prognosis in children after corneal transplant surgery for Peters anomaly type I. Am J Ophthalmol. 2007; 144:104–108.
15. Lowe MT, Keane MC, Coster DJ, Williams KA. The outcome of corneal transplantation in infants, children, and adolescents. Ophthalmology. 2011; 118: 492–497.
16. Martin Al,Hodge C, Lowlessal, Roberts T, Hughes P, Sutton G. Femtosecond laser cataract surgery: Challengin cases. Curr Opin Ophthalmol. 2014; 25:71 -80.
2. Harissi-Dagher M, Colby K. Anterior segment dysgenesis: Peters’ anomaly and sclerocornea. Int Ophthalmol Clin. 2008; 48(2):35-42. Review.
3. Bahn CF, Falls HF, Varley GA, Meyer RF, Edelhauser HF, Bourne WM. Classification of corneal endothelial disorders based on neural crest origin. Ophthalmology.1984; 91(6):558-63.
4. Maillette de Buy Wenniger-Prick LJ, Hennekam RC. The Peters’ plus syndrome: areview. Ann Genet. 2002; 45(2):97-103. Review.
5. Heon E, Barsoum-Homsy M, Cevrette L, Jacob JL, Milot J, Polemeno R, Musarella MA. Peters’ anomaly. The spectrum of associated ocular and systemic malfor-mations. Ophthalmic Paediatr Genet. 1992; 13(2):137-43.
6. Bhandari R, Ferri S, Whittaker B, Liu M, Lazzaro DR. Peters anomaly: review of the literature. Cornea. 2011; 30:939–44.
7. Eguía Martínez Frank et al. Manual de diagnóstico y tratamiento en Oftalmología. La Habana: ECIMED, 2009.
8. KanskyJJ.Oftalmología clínica VIed. España: Ed Elsevier,2006.
9. Ozeki H, Shirai S, Nozaki M, Sakurai E, Mizuno S, Ashikari M, Matsunaga N, Ogura Y: Ocular and systemic features of Peters anomaly. Graefes Arch Clin Exp Opthalmol 2000, 235:833-839.
10. MajanderAS,Lindahi PM,Vasara LK,Krootilla K.Anterior segment optical coherence tomography in congenital corneal opacities. Ophtalmology 2012; 119:2450-2457.
11. Nishide T,Nakanishi M,Hayakawa N,et al.Cataract surgery for tilted lens in Peters anomaly type 2.Case rep. Ophthalmol 2013;4:134- 7.
12. Lorry EA, Porco TC, Naseri A.Cost analysis of virtual – reality phacoemulsification in ophthalmology training programs. J Cataract Refract Surgery 2013; 39 1616- 7.
13. Nischal KK. A new appoach to the clasication of neonatal corneal opacities. Curr Opin Ophthalmol. 2012; 23:344-54.
14. Zaidman GW, Flanagan JK, Furey CC. Long-term visual prognosis in children after corneal transplant surgery for Peters anomaly type I. Am J Ophthalmol. 2007; 144:104–108.
15. Lowe MT, Keane MC, Coster DJ, Williams KA. The outcome of corneal transplantation in infants, children, and adolescents. Ophthalmology. 2011; 118: 492–497.
16. Martin Al,Hodge C, Lowlessal, Roberts T, Hughes P, Sutton G. Femtosecond laser cataract surgery: Challengin cases. Curr Opin Ophthalmol. 2014; 25:71 -80.
Como Citar
1.
Rodríguez Cambas A, Matos López U, Francisco Domingos M, Tirado Soler M. Anomalía de Peters. Presentação dum caso clínico. Rev Inf Cient [Internet]. 2º de março de 2018 [citado 3º de abril de 2025];97(2):362-8. Disponível em: https://revinfcientifica.sld.cu/index.php/ric/article/view/1854
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