Abstract
A 30-year-old female patient presented to our clinic because of lacrimation from an orifice close to the left lower eyelid. Ocular examinations and analyses revealed uterus didelphys and unilateral renal agenesis associated with a left lacrimal fistula. The patient underwent fistulectomy and external dacryocystorhinostomy. We decided to report on this patient owing to the unusual concurrent systemic abnormalities.
References
Birchansky LD, Nerad JA, Kersten RC et al (1990) Management of congenital lacrimal sac fistula. Arch Ophthalmol 108:388
Yuen SJ, Oley C, Sullivan TJ (2004) Lacrimal outflow dysgenesis. Ophthalmology 111(9):1782–1790
Harrison AR, Dailey RA, Wobig JL (2002) Bilateral congenital lacrimal anlage ducts (lacrimal fistula) in a patient with the VACTERL association. Ophthal Plast Reconstr Surg 18(2):149–150
Sullivan TJ, Clarke MP, Brazel S et al (1992) Congenital lacrimal fistula associated with Down’s syndrome. Am J Ophthalmol 113:215–216
Tien AM, Tien DR (2006) Bilateral congenital lacrimal sac fistulae in a patient with ectrodactyly–ectodermal dysplasia–clefting syndrome. J AAPOS 10(6):577–578
Shah S, Shah M, Khandekar R (2010) Management of bilateral congenital lacrimal punctal and canalicular atresia and congenital fistula of the lacrimal sac. Middle East Afr J Ophthalmol 17(2):180–182
Author information
Authors and Affiliations
Corresponding author
Additional information
An erratum to this article is available at http://dx.doi.org/10.1007/s10792-014-0006-x.
Rights and permissions
About this article
Cite this article
Turan-Vural, E., Atmaca, F., Unlu, C. et al. Unilateral lacrimal fistula in a patient with uterus didelphys and renal agenesis. Int Ophthalmol 32, 67–69 (2012). https://doi.org/10.1007/s10792-011-9510-4
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s10792-011-9510-4