Congenital Cyst Eye, One Clinical Case

Souhail H.; Ifrkhas S.; Laktaoui A.

doi:doi:10.11648/j.js.20150303.11

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Congenital Cyst Eye, One Clinical Case

Souhail H., Ifrkhas S., Laktaoui A.

Published in Journal of Surgery (Volume 3, Issue 3)

Received: 31 March 2015 Accepted: 29 April 2015 Published: 12 May 2015

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Abstract

Background: Congenital cyst eye is developmental abnormal arrangement of tissues .It is an extremely rare ocular malformation and is the rare cystic orbital lesion, usually evident at birth and has a varied presentation. A partial or complete failure in the involution of the primary optic vesicle resulting in the formation of a cyst. Case presentation: We report a case of unilateral congenital cystic eye, it was excised completely, and histopathology was confirmed the cystic nature of lesion. Conclusion: congenital cystic eye should be suspected in infants with an unrecognizable ocular globe. It is an extremely rare condition and with only 40 previous cases reported in the literature.

Published in	Journal of Surgery (Volume 3, Issue 3)
DOI	10.11648/j.js.20150303.11
Page(s)	18-20
Creative Commons	This is an Open Access article, distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution and reproduction in any medium or format, provided the original work is properly cited.
Copyright	Copyright © The Author(s), 2015. Published by Science Publishing Group

Keywords

Congenital, Cyst Eye

References

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[2]	Hayashi N, Repka MX, Ueno H, Iliff NT, Green WR. Congenital cystic eye: report of two cases and review of the literature. Surv Ophthalmol. 1999; 44:173–179.
[3]	McLean CJ, Ragge NK, Jones RB, Collin JR. The management of orbital cysts associated with congenital microphthalmos and anophthalmos. Br J Ophthalmol. 2003;87:860–863.
[4]	Shastry BS. Persistent hyperplastic primary vitreous: congenital malformation of the eye. Clin Experiment Ophthalmol. 2009; 37:884–890.
[5]	Tsitouridis I, Michaelides M, Tsantiridis C, Spyridi S, Arvanity M, Efstratiou I. Congenital cystic eye with multiple dermal appendages and intracranial congenital anomalies. Diagn Interv Radiol.2010;16:116–121
[6]	Morselli PG, Morellini A, Sgarzani R, Ghi T, Galassi E. Congenital cystic eye: from prenatal diagnosis to therapeutic management and surgical treatment. J Craniofac Surg. 2011; 22:360–363.
[7]	Mann I: A case of congenital cystic eye. Trans Ophtalmol Soc Aust19391:120–124
[8]	Rainer G, Rüdiger K, Wolfgang E. Congenital cystic eye. Graefe’s Arch Clin Exp Ophthalmol. 2004, 242:268–271.
[9]	Marie-Laure R, Sophie L, Solange M, et al: Une lésion oculaire kystique congénitale exceptionnelle. Ann pathol 2007, 27: 59-60.
[10]	Pillai AM, Rema M. Congenital cystic eye-A case report with CT scan. Indian J Ophthalmol 1987, 35(2): 88-91.
[11]	Pankaj G, Krishna P, Ruchi G. Congenital cystic eye with multiple dermal appendages: a case Report. BMC Ophthalmology 2003, 3:7.
[12]	Goldberg SH, Farber MG, Bullock JD, Crone KR, Ball WS: Bilateral congenital ocular cysts. Ophthalmic Paediatr Genet 1991, 12:31–38
[13]	Raina UK, Tuli D, Arora R, Mehta DK, Bansal R: Congenital cystic eyeball Ophthalmic Surg Lasers 2002, 33:262–263
[14]	Cefalo MG, Colafati GS, Romanzo A, Modugno A, De Vito R, Mastronuzzi A Congenital cystic eye associated with a low-grade cerebellar lesion that spontaneously regressed BMC Ophthalmol. 2014 Jun 17; 14:80. doi: 10.1186/1471-2415-14-80.
[15]	Duke-Elder, S. (1964): System of Ophthalmology Vol.111, Congenital Deformities. Part II, Henry Kimpton London, pp 451 & 481
[16]	Gupta VP, Chaturvedi KU, Sen DK, Govekar KK Congenital cystic eyeball. Indian J Ophthalmol. 1990 Oct-Dec;38(4):205-6.
[17]	Chaudhry IA, Shamsi FA, Elzaridi E, Arat YO, Riley FC. Congenital cystic eye with intracranial anomalies: a clinicopathologic study. Int Ophthalmol. 2007; 27:223–233.
[18]	Mansour AM, Li HK. Congenital cystic eye. Ophthal Plast Reconstr Surg. 1996; 12:104–107.
[19]	Robb RM, Anthony DC. Congenital cystic eye: recurrence after initial surgical removal. Ophthalmic Genet. 2003; 24:117–123.

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APA Style

Souhail H., Ifrkhas S., Laktaoui A. (2015). Congenital Cyst Eye, One Clinical Case. Journal of Surgery, 3(3), 18-20. https://doi.org/10.11648/j.js.20150303.11

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ACS Style

Souhail H.; Ifrkhas S.; Laktaoui A. Congenital Cyst Eye, One Clinical Case. J. Surg. 2015, 3(3), 18-20. doi: 10.11648/j.js.20150303.11

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AMA Style

Souhail H., Ifrkhas S., Laktaoui A. Congenital Cyst Eye, One Clinical Case. J Surg. 2015;3(3):18-20. doi: 10.11648/j.js.20150303.11

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@article{10.11648/j.js.20150303.11,
  author = {Souhail H. and Ifrkhas S. and Laktaoui A.},
  title = {Congenital Cyst Eye, One Clinical Case},
  journal = {Journal of Surgery},
  volume = {3},
  number = {3},
  pages = {18-20},
  doi = {10.11648/j.js.20150303.11},
  url = {https://doi.org/10.11648/j.js.20150303.11},
  eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.js.20150303.11},
  abstract = {Background: Congenital cyst eye is developmental abnormal arrangement of tissues .It is an extremely rare ocular malformation and is the rare cystic orbital lesion, usually evident at birth and has a varied presentation. A partial or complete failure in the involution of the primary optic vesicle resulting in the formation of a cyst. Case presentation: We report a case of unilateral congenital cystic eye, it was excised completely, and histopathology was confirmed the cystic nature of lesion. Conclusion: congenital cystic eye should be suspected in infants with an unrecognizable ocular globe. It is an extremely rare condition and with only 40 previous cases reported in the literature.},
 year = {2015}
}

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TY  - JOUR
T1  - Congenital Cyst Eye, One Clinical Case
AU  - Souhail H.
AU  - Ifrkhas S.
AU  - Laktaoui A.
Y1  - 2015/05/12
PY  - 2015
N1  - https://doi.org/10.11648/j.js.20150303.11
DO  - 10.11648/j.js.20150303.11
T2  - Journal of Surgery
JF  - Journal of Surgery
JO  - Journal of Surgery
SP  - 18
EP  - 20
PB  - Science Publishing Group
SN  - 2330-0930
UR  - https://doi.org/10.11648/j.js.20150303.11
AB  - Background: Congenital cyst eye is developmental abnormal arrangement of tissues .It is an extremely rare ocular malformation and is the rare cystic orbital lesion, usually evident at birth and has a varied presentation. A partial or complete failure in the involution of the primary optic vesicle resulting in the formation of a cyst. Case presentation: We report a case of unilateral congenital cystic eye, it was excised completely, and histopathology was confirmed the cystic nature of lesion. Conclusion: congenital cystic eye should be suspected in infants with an unrecognizable ocular globe. It is an extremely rare condition and with only 40 previous cases reported in the literature.
VL  - 3
IS  - 3
ER  -

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Author Information

Souhail H.

Department of ophthalmology, Military hospital, Meknes Morocco, Faculty of medecine and pharmacy, fes Morocco
Ifrkhas S.

Department of ophthalmology, Military hospital, Meknes Morocco, Faculty of medecine and pharmacy, fes Morocco
Laktaoui A.

Department of ophthalmology, Military hospital, Meknes Morocco, Faculty of medecine and pharmacy, fes Morocco

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APA Style

Souhail H., Ifrkhas S., Laktaoui A. (2015). Congenital Cyst Eye, One Clinical Case. Journal of Surgery, 3(3), 18-20. https://doi.org/10.11648/j.js.20150303.11

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ACS Style

Souhail H.; Ifrkhas S.; Laktaoui A. Congenital Cyst Eye, One Clinical Case. J. Surg. 2015, 3(3), 18-20. doi: 10.11648/j.js.20150303.11

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AMA Style

Souhail H., Ifrkhas S., Laktaoui A. Congenital Cyst Eye, One Clinical Case. J Surg. 2015;3(3):18-20. doi: 10.11648/j.js.20150303.11

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@article{10.11648/j.js.20150303.11,
  author = {Souhail H. and Ifrkhas S. and Laktaoui A.},
  title = {Congenital Cyst Eye, One Clinical Case},
  journal = {Journal of Surgery},
  volume = {3},
  number = {3},
  pages = {18-20},
  doi = {10.11648/j.js.20150303.11},
  url = {https://doi.org/10.11648/j.js.20150303.11},
  eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.js.20150303.11},
  abstract = {Background: Congenital cyst eye is developmental abnormal arrangement of tissues .It is an extremely rare ocular malformation and is the rare cystic orbital lesion, usually evident at birth and has a varied presentation. A partial or complete failure in the involution of the primary optic vesicle resulting in the formation of a cyst. Case presentation: We report a case of unilateral congenital cystic eye, it was excised completely, and histopathology was confirmed the cystic nature of lesion. Conclusion: congenital cystic eye should be suspected in infants with an unrecognizable ocular globe. It is an extremely rare condition and with only 40 previous cases reported in the literature.},
 year = {2015}
}

Copy | Download

TY  - JOUR
T1  - Congenital Cyst Eye, One Clinical Case
AU  - Souhail H.
AU  - Ifrkhas S.
AU  - Laktaoui A.
Y1  - 2015/05/12
PY  - 2015
N1  - https://doi.org/10.11648/j.js.20150303.11
DO  - 10.11648/j.js.20150303.11
T2  - Journal of Surgery
JF  - Journal of Surgery
JO  - Journal of Surgery
SP  - 18
EP  - 20
PB  - Science Publishing Group
SN  - 2330-0930
UR  - https://doi.org/10.11648/j.js.20150303.11
AB  - Background: Congenital cyst eye is developmental abnormal arrangement of tissues .It is an extremely rare ocular malformation and is the rare cystic orbital lesion, usually evident at birth and has a varied presentation. A partial or complete failure in the involution of the primary optic vesicle resulting in the formation of a cyst. Case presentation: We report a case of unilateral congenital cystic eye, it was excised completely, and histopathology was confirmed the cystic nature of lesion. Conclusion: congenital cystic eye should be suspected in infants with an unrecognizable ocular globe. It is an extremely rare condition and with only 40 previous cases reported in the literature.
VL  - 3
IS  - 3
ER  -

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