Volume 93, Issue S255
ABS15-0574
Free Access

Three optic disc pit maculopathy case studies by optical coherence tomography images supporting the role of cerebrospinal fluid in this pathology

M. Martinez

M. Martinez

Ophthalmology, Lozano Blesa” University Clinic Hospital, Zaragoza, Spain

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J. Ascaso

J. Ascaso

Ophthalmology, Lozano Blesa” University Clinic Hospital, Zaragoza, Spain

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L. Arias

L. Arias

Ophthalmology, Hospital Universitari de Bellvitge, Barcelona, Spain

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A. Filloy

A. Filloy

Ophthalmology, Hospital Universitari de Bellvitge, Barcelona, Spain

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C. Almenara

C. Almenara

Ophthalmology, Lozano Blesa” University Clinic Hospital, Zaragoza, Spain

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O. Esteban

O. Esteban

Ophthalmology, Lozano Blesa” University Clinic Hospital, Zaragoza, Spain

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M. Del Buey

M. Del Buey

Ophthalmology, Lozano Blesa” University Clinic Hospital, Zaragoza, Spain

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J. Cristobal

J. Cristobal

Ophthalmology, Lozano Blesa” University Clinic Hospital, Zaragoza, Spain

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First published: 23 September 2015

Abstract

Purpose

Optic disc pit (ODP) is a rare congenital optic disc abnormality characterized by a localized grayish-white depression usually in the center or inferotemporal part of the optic nerve head. It is generally unilateral (85-90%) and its prevalence is estimated to be 1 in 11,000. Unless the ODP develops maculopathy, patients remain asymptomatic. Serous macular detachment may occur in up to 50% of cases,leading to significant decrease in visual acuity. Although the pathogenesis of ODP maculopathy is unclear, various theories about its onset have implicated fluid entry either from the vitreous cavity or from leakage of cerebrospinal fluid through the peripapillary subarachnoid space. The aim of this study was to evaluate the source of subretinal fluid under the macula in three patients with ODP.

Methods

Three different optical coherence tomography equipments (EDI-OCT Spectralis, Heidelberg; Swept-source OCT, Topcon and Spectral-domain 3D OCT-2000, Topcon) were used.

Results

These OCT images revealed a direct communication between a prominent serous macular detachment and the subarachnoid space through the ODP.

Conclusions

These three cases support the theory that in some cases the source of serous macular detachment could be cerebrospinal fluid passing into the retina through the ODP due to an incomplete closure of the embryonic fissure.

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