|Year : 2018 | Volume
| Issue : 3 | Page : 177-179
Acquired pit of the optic nerve in primary angle-closure glaucoma
Sadiqha Banu Shaik, Kavitaa Ramamoorthy, Pratheeba Devi Nivean, Murali Ariga
Department of Ophthalmology, M N Eye Hospital, Chennai, Tamil Nadu, India
|Date of Web Publication||23-Oct-2018|
M N Eye Hospital, Chennai, Tamil Nadu
Source of Support: None, Conflict of Interest: None
Herein, we report a case of acquired optic nerve pit in a 46-year-old Indian male, a known case of primary angle closure glaucoma (PACG) compatible with treatment for the past 15 years. He presented to our clinic with complaints of recent decrease in vision; on examination, his visual acuity was found correctable to 6/6 and 6/12 in the right and left eye, respectively. Fundoscopy revealed glaucomatous cupping in both the eyes and subretinal fluid in macula of the left eye. Swept-source optical coherence tomography macula and retinal nerve fiber layer disclosed acquired pit of the optic nerve (APON) in the left eye. The patient was under continuous follow-up and maculopathy spontaneously resolved. An APON may indicate progression of glaucoma and was more commonly reported in cases of primary open-angle glaucoma; we aimed to report an unusual presence of APON in a case of PACG.
Keywords: Acquired optic nerve pit, primary open-angle glaucoma, primary angle-closure glaucoma
|How to cite this article:|
Shaik SB, Ramamoorthy K, Nivean PD, Ariga M. Acquired pit of the optic nerve in primary angle-closure glaucoma. TNOA J Ophthalmic Sci Res 2018;56:177-9
|How to cite this URL:|
Shaik SB, Ramamoorthy K, Nivean PD, Ariga M. Acquired pit of the optic nerve in primary angle-closure glaucoma. TNOA J Ophthalmic Sci Res [serial online] 2018 [cited 2020 Jun 4];56:177-9. Available from: http://www.tnoajosr.com/text.asp?2018/56/3/177/243765
| Introduction|| |
Dr. Weithe first described the clinical presentation of two optic disc depressions in a 62-year-old woman in 1882, which later has been addressed as optic disc pit (ODP). We present this case for the rare nature of the disease, so ophthalmologists can be vigilant as its appearance may indicate progression of glaucoma and comes with complications such as serous maculopathy which presents as schisis-like cavities in the outer retina.
| Case Report|| |
A 46-year-old Indian male with known case of primary angle closure glaucoma (PACG) for the past 15 years was on the treatment with bimatoprost and beta-blocker combination in both eyes post-YAG peripheral iridotomy (PI). The patient had complaints of recent onset of decreased vision in the left eye; his visual acuity was correctable to 6/6 and 6/12 in the right and left eye, respectively; pupils were equally round and reactive. No relative afferent pupillary defect was observed. Intra-ocular pressure using Goldmann applanation tonometry was 14 mmHg in both eyes. Anterior segment revealed patent YAG PI and there were no other remarkable changes on fundus examination. Glaucomatous cupping of 0.8 was noted in both eyes and subretinal fluid in the left macula [Figure 1]a. Visual field showed paracentral arcuate scotoma [Figure 1]b.
To unearth the cause of sub-retinal fluid (SRF) and decreased vision in the left eye, swept-source optical coherence tomography (OCT) macula and retinal nerve fiber layer (RNFL) were done, and to our surprise, it was acquired optic nerve pit. Subsequently, expert opinion from retina consultants was sought for further management of maculopathy [Figure 2] and [Figure 3].
The patient was asked to discontinue bimatoprost and to continue timolol for the left eye and was advised for continuous follow-up for 3 months; on review of 3 months, visual acuity was correctable to 6/6 N6 in both eyes, and there was spontaneously resolving maculopathy of the left eye, optic nerve pit remain unchanged [Figure 4].
As the possibility of recurrent maculopathy and serous retinal detachment secondary ODP remains, the patient was asked for continuous follow-up and to report immediately if any visual changes.
| Discussion|| |
Early, reliable signs of glaucomatous damage can be provided through keen observation of structural changes of the optic disc-nerve fiber layer complex. These structural patterns of optic nerve damage have been used to subclassify glaucoma patients.,
An acquired pit of the optic nerve (APON) also appears to be a distinct pattern of optic nerve damage that can be used as a reliable sign of glaucoma.
APON is a deep, localized excavation of the neural rim with a sharply localized depression and loss of the normal laminar architecture of the lamina cribrosa. There is an increased incidence of acquired pits in patients with low-tension glaucoma versus patients with typical glaucoma. The lamina cribrosa is thought to be more susceptible to damage from intraocular pressure in patients with low-tension glaucoma versus normal-tension glaucoma.,
Lincoff et al. suggested that the fluid from optic pits could initially form a schisis-like cavity and then be complicated secondarily by an outer layer detachment and subretinal fluid. Serous macular detachments carry a worse prognosis.,
Serous macular elevations develop in approximately 25%–75% of eyes with pits.,,, Spontaneous resolution of ODP-Maculopathy (ODP-M) with recovery of excellent visual acuity has been reported.,
Our case is also consistent that ANOP appears to be more prevalent in low-tension glaucoma.
The number of treatment options has been reported for serous retinal detachments that may occur in combination with ODPs such as observation, laser photocoagulation, intravitreal tamponade with gas or silicone oil, vitrectomy with internal limiting membrane peeling, and gas tamponade.,
In our case, there was spontaneous resolving of maculopathy and the optic nerve pit remains unchanged.
| Conclusion|| |
Among patients with glaucoma, patients with APON represent a subgroup who are at increased risk for progressive optic disk damage and visual field loss, so careful stereoscopic observation may lead to the diagnosis; however, additional testing such as OCT imaging is helpful in appreciating the depth of pitting and the potential conduit to the subsensory retinal space. This is an unusual presentation of acquired optic nerve pit in PACG.
To the best of our knowledge, such a case has not been reported previously in literature.
Declaration of patient consent
The authors certify that they have obtained all appropriate patient consent forms. In the form the patient(s) has/have given his/her/their consent for his/her/their images and other clinical information to be reported in the journal. The patients understand that their names and initials will not be published and due efforts will be made to conceal their identity, but anonymity cannot be guaranteed.
Financial support and sponsorship
Conflicts of interest
There are no conflicts of interest.
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[Figure 1], [Figure 2], [Figure 3], [Figure 4]