==== Front Rom J Ophthalmol Rom J Ophthalmol RomJOphthalmol Romanian Journal of Ophthalmology 2457-4325 2501-2533 Romanian Society of Ophthalmology Romania RomJOphthalmol-64-449 10.22336/rjo.2020.69 Case Reports Unilateral optic disc drusen mis-diagnosed as optic neuritis: Diagnostic and therapeutic implications Bontzos Georgios * Smoustopoulos Georgios * Detorakis Theocharis Efstathios * * Department of Ophthalmology, Medical School, University of Crete, Heraklion, Greece Correspondence to: Georgios Bontzos, MD, Department of Ophthalmology, Medical School, University of Crete, Heraklion, 71003 Voutes, Heraklion, Greece, Phone: +302 810 392 730, E-mail: gbontzos@hotmail.gr Oct-Dec 2020 64 4 449 454 ©Romanian Society of Ophthalmology 2020This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.Objective: To present a case of unilateral optic disc drusen, initially mis-diagnosed as optic neuritis, which led to chronic systemic administration of steroids and the development of hypercortisolism. Methods: A 22-year-old female was referred because of the lack of improvement of the manifestations of optic neuritis despite the chronic use of systemic steroids. Presence of unilateral optic disc edema was initially observed, associated with ipsilateral scotomata and increased ipsilateral latency time in visually evoked potentials (VEP). Results: A CT scan, A and B ultrasonography and autofluorescence of the optic disc confirmed the diagnosis of optic disc drusen. Conclusions: In cases of optic disc edema, the possibility of drusen should always be examined even if functional disturbances, such as scotomas in visual fields or electrophysiological findings, are present, to avoid potential toxicity from unnecessary medications. optic-discdrusenpseudo-papilledema ==== Body Introduction Optic disc drusen are acellular calcifications of the optic disc, either superficial or deep, occurring in up to 2% of the general population [1]. The lesions are bilateral in 75% of the cases and may increase in size in aging individuals [1]. Usually they are asymptomatic, however, they may occasionally cause vascular disorders, such as haemorrhages, retinal vein occlusion or venous stasis retinopathy [2,3]. It should be noted that the most significant clinical implication of optic disc drusen is the fact that they might be confused with true optic disc edema [4]. We presented a case of young woman with unilateral optic disc drusen associated with ipsilateral visual field defects and increased ipsilateral latency time in visually evoked potentials (VEP), who was mis-diagnosed as suffering from optic neuritis for which she received large amounts of steroids with considerable systemic morbidity. Case Report A 22-year-old female was referred to the Department of Ophthalmology of the University Hospital of Heraklion due to persistent edema of the right optic disc (Fig. 1A). Previous systemic and ophthalmic histories were non-contributory. The edema of the right optic disc was discovered during a routine ophthalmic examination for glasses prescription and was confirmed by an OCT examination (Fig. 1C, D). Fig. 1 Fundus color photos of right (A) and left (B) eyes, showing irregular fluffy borders of the optic disc of the right eye. OCT scan (C,D) of the optic disc area of the right eye, shows elevation of the optic disc Subsequently, the patient underwent visual field testing, which was significant for scotomata at the visual field of the right eye (Fig. 2). Accordingly, her ophthalmologist referred her to a neurologist for further evaluation. Taking into account the presence of unilateral optic disc edema with associated visual field defects and her young age, the possibility of optic neuritis was raised and the patient underwent MRI and MR angiography of the brain (Fig. 3), which were however, non-contributory. The patient then underwent checkerboard VEP, which confirmed an increased latency time interval for the right eye, compared with the left eye (Fig. 4A). At that point, the diagnosis of optic neuritis of unspecified origin was considered highly likely and the patient was administered systemic steroids for 3 months in a tapering dosage. However, steroid treatment did not improve visual field findings. Moreover, the optic disc edema persisted and the patient was referred to the Department of Ophthalmology for further management. Fig. 2 Visual fields (30°) of the right (A) and left (B) eyes, showing a scotoma at the superior-nasal quadrant of the visual fields of the right eye Fig. 3 MRI scans of the orbits of the patient. T1-oriented contrast enhanced and fat suppressed scan (A), T-2 oriented scan (B), both at transverse planes. T1-oriented sagittal plane scan (D). MR angiography of the brain (C). All scans are non-contributory concerning orbital or intracranial pathology Fig. 4 Output of checkerboard VEP of both eyes showing an increased latency time for the right eye Upon presentation, facial edema was noted, compatible with steroid-related Cushing’s syndrome. Best corrected visual acuity (BCVA) was 20/ 20 OU, color perception was normal and the IOP was 18 mmHg (OD) and 17 mmHg (OS) without medications. Slit lamp biomicroscopy was non-contributory. Fundoscopy was indeed significant for optic disc edema (OD) with normal appearance of the optic disc for the OS. However, considering the lack of changes in the appearance of the optic disc, following administration of steroids and the fact that BCVA or color vision were not compromised, the suspicion of optic disc drusen was raised. Accordingly, B-scan and A-scan ultrasound evaluations were performed (Fig. 5A), which confirmed the presence of a highly reflective area at the optic disc of the right eye. Moreover, CT imaging (Fig. 5B) and auto-fluorescence (Fig. 5C,D) were significant for the presence of a fluorescent body and high density area, respectively, on the right optic disc. Therefore, the presence of the optic disc drusen was confirmed. Fig. 5 A and B ultrasound scans of the right eye showing a highly reflective area at the optic nerve head, compatible with drusen (A). CT scan of the orbits showing a bone density area at the optic nerve head of the right eye (B). Auto-fluorescence fundoscopic images of the right (C) and left (D) eyes, showing fluorescent bodies at the optic nerve head of the right eye, compatible with drusen Discussion Optic disc drusen often present as an incidental finding in routine clinical practice [5]. The problem of the differential diagnosis of optic disc drusen from true optic disc edema is more complicated in children, due to the fact that in this age group optic disc drusen may occasionally co-exist with intracranial hypertension [6,7]. Moreover, optic disc drusen have been associated with various clinical ophthalmic findings, such as abnormal vascular branching, cilioretinal vessels, peripapillary atrophy and haemorrhages [8]. Visual fields defects, relative afferent pupillary defects and an increased latency time in multi-focal VEP have also been associated with optic disc drusen in previous reports [9,10]. Such changes may be associated with compression on the optic nerve fibers, caused by the accumulation of calcified deposits in a tight space, such as the optic nerve head [10]. In the case presented, the diagnostic uncertainties associated with the finding of a unilateral optic disc edema and the obvious concern of physicians who initially treated the patient not to miss an important diagnosis, such as an episode of optic neuritis, led to the administration of systemic steroids, which in turn resulted in serious side-effects (the development of Cushing’s syndrome). This is also the reason why additional diagnostic modalities, such as VEPs or MR angiographic studies, were employed to evaluate this condition. Ironically, the presence of optic disc drusen would have been obvious if simpler diagnostic methods, such as A and B ultrasound scans or CT scans were initially employed. Therefore, primary care providers, either ophthalmologists or optometrists, should bear in mind that optic disc elevation or blurred margins, even when associated with findings such as visual field defects, could be the result of optic disc drusen and accordingly employ adequate available diagnostic modalities (such as ultrasound and CT scans) before referring the patient to tertiary facilities for further management. Conclusion Optic disc drusen are a well-known cause of pseudo-papilledema. Although, typically asymptomatic, common manifestations include peripheral scotomas that are abnormal pupillary reflexes. Suspicion of this entity is raised by careful clinical examination and patient’s history. Diagnosis can be confirmed by autofluorescence or ultrasonography. Conflict of Interest The authors state no conflict of interest. Informed Consent An informed consent was obtained from the patient included in this Case Report. Authorization for the use of human subjects The research related to human use complies with all the relevant national regulations, institutional policies, is in accordance with the tenets of the Helsinki Declaration, and has been approved by the Ethics Committee of the Department of Ophthalmology of the University Hospital of Heraklion. Acknowledgements None. Sources of Funding None. Disclosures None. ==== Refs 1 Arbabi EM Fearnley TE Carrim ZI Drusen and the misleading optic disc Pract Neurol 2010 10 27 30 20130293 2 Austin JK Optic disc drusen and associated venous stasis retinopathy J Am Optom Assoc 1995 66 91 95 7714318 3 Gallagher MJ Clearkin LG Drug or drusen? Central retinal vein occlusion in a young healthy woman with disc drusen Eye (Lond) 2000 14 401 402 11027015 4 Sarac O Tasci YY Gurdal C Differentiation of optic disc edema from optic nerve head drusen with spectral-domain optical coherence tomography J Neuroophthalmol 2012 32 207 211 22473041 5 Vaphiades MS Diagnostic uncertainty due to optic disc drusen J Neuroophthalmol 2012 32 145 147 22297266 6 Komur M Sari A Okuyaz C Simultaneous papilledema and optic disc drusen in a child Pediatr Neurol 2012 46 187 188 22353297 7 Krasnitz I Beiran I Mezer E Miller B Coexistence of optic nerve head drusen and pseudotumor cerebri: a clinical dilemma Eur J Ophthalmol 1997 7 383 386 9457463 8 Flores-Rodríguez P Gili P Martín-Ríos MD Ophthalmic features of optic disc drusen Ophthalmologica 2012 228 59 66 22584542 9 Frangie JP Nepomnyaschy N Visual field loss and a relative afferent pupillary defect in a patient with optic nerve head drusen J Ophthalmic Nurs Technol 1991 10 194 200 1942098 10 Grippo TM Ezon I Kanadani FN Wangsupadilok B Tello C Liebmann JM Ritch R Hood DC The effects of optic disc drusen on the latency of the pattern-reversal checkerboard and multifocal visual evoked potentials Invest Ophthalmol Vis Sci 2009 50 4199 4204 19182248