Introduction: Congenital optic disc anomalies in children refer to structural variations of the optic nerve head present from birth. These deformations involve the size, shape, color, and vessels of the optic disc. Although often asymptomatic, these anomalies can impact the visual development of the child, underscoring the importance of a thorough fundus examination for early detection and appropriate medical follow-up. We present two cases of congenital optic disc anomalies in children, illustrating the diagnostic challenges and complexity of their management. Case 1: A 3-year-old girl presented with a white spot in her left eye present since birth. Uncorrected distance visual acuity was 2/10 in the right eye, while she could perceive hand movements at 2 meters with the left eye. Normal examination in the right eye showed leukocoria, microphthalmia, and a white mass at the center of the optic disc on fundus examination in the left eye. Ocular imaging, including ultrasound and optical coherence tomography (OCT), confirmed the diagnosis of persistent hyperplastic primary vitreous (PHPV) in its mixed form in the left eye. Management included prescribing full optical correction and functional rehabilitation, without resorting to surgery. The course was marked by persistent amblyopia leading to a poor prognosis. Case 2: A 7-year-old girl consulted for vision disturbance in her right eye. Visual acuity was finger counting at 2 meters in the right eye and 10/10 in the left eye. Anterior segment examination revealed no abnormalities in both eyes. However, fundus examination highlighted a large funnel-shaped excavation associated with central glial proliferation, wheel spoke vessels, and neuroretinal ring atrophy in the right eye. Optical coherence tomography (OCT) of the right eye confirmed the diagnosis of isolated unilateral Morning Glory syndrome. Management included full optical correction and orthoptic rehabilitation. The course was marked by the absence of ocular complication and maintenance of visual stability in the right eye. The prognosis seemed favorable. Conclusion: Congenital optic disc anomalies in children exhibit great clinical variability and require an individualized diagnostic and therapeutic approach.
References
[1]
Denis, D., Hugo, J., Beylerian, M., Ramtohul, P., Aziz, A., Matonti, F. AND Lebranchu, P. (2019) Les anomalies congénitales de la papille. Journal Français d’Ophtalmologie, 42, 778-789. https://doi.org/10.1016/j.jfo.2018.09.011
[2]
Brémond-Gignac, D. and Milazzo, S. (2011) Les anomalies congénitales du nerf optique de l’enfant. Les Cahiers d’Ophtalmologie, 146, 33-34. https://doi.org/10.1016/j.jfo.2011.02.013
[3]
Mohand, M.S., Bouaziz, T. and Juvespan, M. (2002) Morning Glory Syndrome: À propos d’une observation. Journal Françaisd’Ophtalmologie, 25, 90-99.
[4]
Loudot, C., Fogliarini, C., Baeteman, C., Mancini, J., Girard, N. and Denis, D. (2007) Rehabilitation on Functional Amblyopia in Morning Glory Syndrome. Journal Françaisd’Ophtalmologie, 30, 998-1001. https://doi.org/10.1016/S0181-5512(07)79276-8
[5]
Roche, O., Keita Sylla, F., Beby, F., Orssaud, C. and Dufier, J.L. (2007) Persistance et hyperplasie du vitré primitif. Journal Français d’Ophtalmologie, 30, 647-657. https://doi.org/10.1016/S0181-5512(07)89674-4
[6]
Ahmiti, S., Ahbeddou, M., El khaoua, N., Tzili, F., Alami, F. and Bencherifa, A.B. (2013) Persistance et hyperplasie du vitré primitif. Maroc Médical, 35, 252-261.
[7]
Silbert, M. and Gurwood, A.S. (2000) Persistent Hyperplastic Primary Vitreous: Clinical Review. Clinical Eye and Clinical Care, 12, 131-137. https://doi.org/10.1016/S0953-4431(00)00054-0
[8]
Alexandrakis, G., Scott, I.U., Flynn Jr., H.W., Murray, T.G. and Feuer, W.J. (2000) Visual Acuity Outcomes with and without Surgery in Patients with Persistent Fetal Vaculature. Ophthalmology, 107, 1068-1072. https://doi.org/10.1016/S0161-6420(00)00100-7
[9]
Chan, R.T., Chan, H.H. and Collin, H.B. (2002) Morning Glory Syndrome. Clinical and Experimental Optometry, 85, 383-388. https://doi.org/10.1111/j.1444-0938.2002.tb02390.x
[10]
Kumar, J., Adenuga, O.O., Singh, K., Ahuja, A.A., Kannan, N.B. and Ramasamy, K. (2021) Clinical characteristics of Morning Glory Disc Anomaly in South India. Taiwan Journal of Ophthalmology, 11, 57-63. https://doi.org/10.4103/tjo.tjo_52_20
[11]
Abdoulaye, N. and Kolé, S.M. (2017) Le syndrome du soleil levant. Pan African Medical Journal, 26, Article 176. https://doi.org/10.11604/pamj.2017.26.176.11445
[12]
Kouassi, F.X., Koman, C.E., Diomandé, I.A., Somahoro, M., Sowagnon, T.Y.C., Kra, A.N.S. and Koffi, K.V. (2017) Morning Glory Syndrome: A Case Report. Journal of Ophthalmology, 2, Article ID: 000129.
[13]
Ceynowa, D.J., Wickström, R., Olsson, M., Eriksson, U., Wiberg, M.K. and Fahnehjelm, K.T. (2015) Morning Glory Disc Anomaly in Childhood—A Population-Based Study. ActaOphthalmologica, 93, 626-634. https://doi.org/10.1111/aos.12778
[14]
Harasymowycz, P., Chevrette, L., Décarie, J.C., Hanna, N., Aroichane, M., Jacob, J.L., Milot, J. and Homsy, M. (2005) Morning Glory Syndrome: Clinical, Computerized Tomographic, and Ultrasonographic Findings. Journal of Pediatric Ophthalmology & Strabismus, 42, 290-295. https://doi.org/10.3928/0191-3913-20050901-11
[15]
Fei, P., Zhang, Q., Li, J. and Zhao, P. (2013) Clinical Characteristics and Treatment of 22 Eyes of Morning Glory Syndrome Associated with Persistent Hyperplastic Primary Vitreous. British Journal of Ophthalmology, 97, 1262-1267. https://doi.org/10.1136/bjophthalmol-2013-303565
[16]
Schneider, C., Cayrol, D., Arnaud, B. and Schmitt Bernard, C.F. (2002) Forme Clinique de l’anomalie papillaire en fleur de liseron ou Morning Glory Syndrome. Journal Français d’Ophtalmologie, 25, 178-181.