A rare case of congenital corneal clouding with anterior staphyloma of the eye
Abstract
There are only few case reports of congenital anterior staphyloma, an extremely rare condition. We report a case of congenital anterior staphyloma presenting as corneal clouding. A preterm girl baby was noted at birth to have bilateral corneal opacity with left sided microcornea. Ophthalmological evaluation revealed anterior staphyloma in right eye &total leucomatous corneal opacity in left eye. Despite antiglaucoma treatment, right sided bupthalmos & corneal thinning worsened. Corneal transplant was done at 7 months of age & baby improved symptomatically.Congenital anterior staphyloma occurs due to developmental aberration or secondary to inflammation. There are various genetic, metabolic, developmental & idiopathic causes of congenital corneal clouding like congenital glaucoma, birth trauma, peters anomaly, dermoid tumors, sclerocornea, infectious/inflammatory processes, metabolic causes & excess prenatal maternal consumption of alcohol. Complete evaluation of congenital corneal clouding include slit lamp biomicroscopy, funduscopy, tonometry, gonioscopy, ultrasonography, photo screening, ultrasound biomicroscopy & CT scanning in selected cases. Treatment is primarily surgical followed by management of amblyopia & optical therapy. Early penetrating keratoplasty, primary combined trabeculotomy-trabeculectomy & corneal grafting are associated with a favorable visual outcome. Early identification of ophthalmological problems in infancy & prompt intervention is mandatory for conditions like congenital corneal clouding.
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References
2. Parsons J. (1904): Trans, Oph. Soc. U.K. P. 47, Cited by Duke-Elder, S. (1964).
3. Duke-Elder, S. (1964): System of Ophthalmology, Vol.III (Part 2) p. 523-27. Henry Kimpton, London.
4. Gupta A K, Patnaik B, Agarwal, L.P. (1965): Orient. A. Oph. 3, 105.
5. Runte (1903): Arch. Augenh, 48, 62.
6. Mann, Ida (1957): Developmental abnormalities of the eyes", 2nd Edition.P. 347, 355.British Medical Association House, Tavistock, Square, London W.C.1. [PubMed]
7. Hwang JM, Chung DC, Traboulsi EI. A new syndrome of hereditary congenital corneal opacities, cornea guttata, and corectopia.Arch Ophthalmol. 2003 Jul. 121(7):1053-4. [PubMed]
8. Kottler U, Demir D, Schmidtmann I, Beck M, Pitz S. Central corneal thickness in mucopolysaccharidosis II and VI. Cornea. 2010 Mar;29(3):260-2. doi: 10.1097/ICO.0b013e3181b55cc1. [PubMed]
9. Kim T, Cohen EJ, Schnall BM, Affel EL, Eagle RC Jr. Ultrasound biomicroscopy and histopathology of sclerocornea. Cornea. 1998 Jul;17(4):443-5. [PubMed]
10. Coulson-Thomas VJ, Caterson B, Kao WW. Transplantation of human umbilical mesenchymal stem cells cures the corneal defects of mucopolysaccharidosis VII mice. Stem Cells. 2013 Oct;31(10):2116-26. doi: 10.1002/stem.1481. [PubMed]
11. Reidy JJ. Penetrating keratoplasty in infancy and early childhood.CurrOpinOphthalmol. 2001 Aug;12(4):258-61. [PubMed]
12. Mandal AK, Gothwal VK, Bagga H, Nutheti R, Mansoori T. Outcome of surgery on infants younger than 1 month with congenital glaucoma. Ophthalmology. 2003 Oct;110(10):1909-15.
Copyright (c) 2016 Author (s). Published by Siddharth Health Research and Social Welfare Society
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