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Optic Nerve Diastasis in a Patient With CongenitalOptic Nerve HypoplasiaAmit Gaur, MD, FRCS,a David Squirell, MRCOphth,a John P. Burke, FRCS,a andPaul D. Griffiths, PhD, FRCRb

Congenital optic nerve hypoplasia (ONH) is a relatively common,nonprogressive, developmental abnormality of the eye and has be-come recognized as a major cause of blindness in children.1 Al-though it may occur as an isolated event, a wide range of neurologicand endocrine abnormalities may be associated with ONH. Wepresent a case of congenital ONH in which optic nerve diastasis wasobserved on magnetic resonance imaging.

A 10-month-old boy presented with intermittent leftexotropia of 3 months’ duration. His visual acuitywas 6/12, with both eyes open as measured by

Cardiff cards (Keeler Ltd., Windsor, UK) at 1 m. A strongobjection to right eye occlusion was noted. Ocular exam-ination revealed poor fixation with the left eye, full ocularmovements, normal anterior segments, a comitant 50� leftexotropia, normal fundi, and no significant refractive er-ror. A diagnosis of left exotropia with possible amblyopiawas made. Right eye occlusion was advised, and the boywas monitored. A year later, when more accurate visiontesting with Kay Picture test (Kay Pictures, Tring, Herts,UK) was possible, the visual acuity in the his left eye wasnoted to be 1/60, whereas it was 6/6 in the right eye. A 10to 20� left exotropia was noted, and poor fixation with theleft eye and objection to occlusion of the right eye per-sisted. On fundus examination, the right eye was normal,whereas the left optic nerve was hypoplastic. Electrophysi-ologic testing revealed subnormal visual-evoked responsesto left-eye stimulation.

MRI of the brain and orbit confirmed that the left opticnerve was hypoplastic all the way back to the optic chiasm(Figure 1 A). No evidence was found of any other intra-cranial abnormalities, such as the absence of the corpuscallosum or a mass lesion relating to the optic apparatus.High-resolution T2-weighted images showed that a shortsegment (approximately 4 mm) of the left optic nerve wasdiastatic within the optic canal. The optic sheath wasdeformed in the vicinity of the diastasis as shown in Figure1B. At the last follow-up visit in January 2004, visual acuity

Author affiliations: aDepartment of Ophthalmology, bAcademic Unit of Radiology, RoyalHallamshire Hospital, Sheffield, United Kingdom

Submitted February 28, 2005.Revision accepted April 26, 2006.Reprint requests: Dr. A. Gaur, MD, FRCS, 15 Coed Y Wenallt, Cardiff, UK,

CF14 6TN (email: [email protected]).J AAPOS 2006;10:482-483.

Copyright © 2006 by the American Association for Pediatric Ophthalmology andStrabismus.

1091-8531/2006/$35.00 � 0doi:10.1016/j.jaapos.2006.04.006

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in the patient’s left eye was 1/60, with persistent inabilityto take up fixation and an exotropia of 15�.

DiscussionMRI confirmed the diagnosis of ONH in our case de-scribed here. This method is reliable to confirm opticnerve and chiasmatic hypoplasia.2 It is important for theophthalmologist to recognize that ONH may be associ-ated with extended pathology in the central nervous sys-

FIG 1. Coronal high-resolution T2-weighted images through the opticnerve. The more anterior image (A) shows left ONH. Note that on thissequence cerebrospinal fluid has a high signal (white) and the nerve itselfis low signal ( black). More posteriorly (B) the nerve is split into two, andthe optic sheath is deformed from its usual rounded configuration,resembling a heart shape, lying on its side.

tem. An important clinical association of ONH with mid-

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line cerebral defects, such as absence of the septum pelluci-dum, agenesis of the corpus callosum, dysplasia of theanterior third ventricle, and hypopituitarism, is referred to assepto-optic dysplasia.3 With the advent of high-resolutionneuroimaging, it is now appreciated that ONH may be as-sociated with a wider spectrum of central nervous systemmalformations. Structural central nervous system abnormal-ities on computed axial tomography brain scans were de-scribed in 90% of cases with ONH in a series that includedagenesis of the corpus callosum, porencephaly, diffuse cere-bral and cerebellar atrophy, cystic paraventricular leukoma-lacia, suprasellar arachnoid cyst, schizencephaly, aqueductstenosis, hydrocephalus, and holoprosencephaly.4 MRI hasbeen shown to be a more sensitive modality for detectingintracranial abnormalities in patients with ONH.5 Reportsusing magnetic resonance imaging in ONH have shownposterior pituitary ectopia, infundibular hypoplasia, and ce-rebral hemispheric abnormalities, which included schizen-cephaly, cortical heterotropia, posterior fossa arachnoid cyst,periventricular leucomalacia, and diffuse encephalomala-cia.5-8

The left ONH in our case was associated with opticnerve diastasis. Optic nerve splitting has been describedafter trauma and penetration by an aneurysm.9,10 Ourreview of literature* revealed no previous report of con-genital optic nerve diastasis or its association with ONH.

*A search was conducted on PubMed using the terms optic nerve,hypoplasia, intracranial abnormalities, anomalies, congenital, splitting,

diastasis, dehiscence, MRI, and computed tomographic scans.

Journal of AAPOS

References

1. Lambert SR, Hoyt CS, Narahara MH. Optic nerve hypoplasia. SurvOphthalmol 1987;32:1-9.

2. Brodsky MC, Glasier CM, Pollock SC, Angtuago EJC. Optic nervehypoplasia: identification by magnetic resonance imaging. ArchOphthalmol 1990;108:1562-7.

3. Roessmann U. Septo-optic dysplasia (SOD) of DeMorsier syndrome.J Clin Neurol Ophthalmol 1985;9:156-9.

4. Burke JP, O’Keefe M, Bowell R. Optic nerve hypoplasia, encepha-lopathy, and neurodevelopmental handicap. Br J Ophthalmol 1991;75:236-9.

5. Brodsky MC, Glasier CM. Optic nerve hypoplasia: clinical signifi-cance of associated central nervous system abnormalities on magneticresonance imaging. Arch Ophthalmol 1993;111:66-74.

6. Kuban KCK, Teele RL, Wallman J. Septo-optic-dysplasia-schizen-cephaly: radiographic and clinical features. Pediatr Radiol 1989;19:145-50.

7. Kelly WM, Kucharczyk W, Kucharczyk J, et al. Posterior pituitaryectopia: an MR feature of pituitary dwarfism. AJNR Am J Neurora-diol 1988;9:453-60.

8. Kaufman LM, Miller MT, Mafee MF. Magnetic resonance imagingof pituitary staff hypoplasia: a discrete midline anomaly associatedwith endocrine abnormalities in septo-optic dysplasia. Arch Ophthal-mol 1989;107:1485-9.

9. Dinkel TA, Ward TP, Frey DM, Hollifield RD. Dissection along theoptic nerve axis by a BB. Arch Ophthalmol 1997;115:673-5.

10. Kanamaru K, Ishida F, Taki W. Splitting and penetration of the opticnerve by an aneurysm arising from the anterior wall of internal carotidartery: case report. J Neurol Neurosurg Psychiatry 2001;71:525-7.


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