Indian Journal of Ophthalmology

ONE MINUTE OPHTHALMOLOGY
Year
: 2018  |  Volume : 66  |  Issue : 11  |  Page : 1531-

Unilateral macular drusen in a young female


Kareem Sioufi1, Katherine E Talcott2, Marc J Spirn2,  
1 The Retina Service of Wills Eye Hospital, Mid Atlantic Retina, Philadelphia, Pennsylvania, PA, USA; Storm Eye Institute, Medical University of South Carolina, Charleston, South Carolina, USA
2 The Retina Service of Wills Eye Hospital, Mid Atlantic Retina, Philadelphia, Pennsylvania, PA, USA

Correspondence Address:
Dr. Kareem Sioufi
Retina Service, Wills Eye Hospital, Thomas Jefferson University, 840 Walnut Street, Philadelphia, 19107-5109 PA
USA




How to cite this article:
Sioufi K, Talcott KE, Spirn MJ. Unilateral macular drusen in a young female.Indian J Ophthalmol 2018;66:1531-1531


How to cite this URL:
Sioufi K, Talcott KE, Spirn MJ. Unilateral macular drusen in a young female. Indian J Ophthalmol [serial online] 2018 [cited 2019 Jul 22 ];66:1531-1531
Available from: http://www.ijo.in/text.asp?2018/66/11/1531/244039


Full Text



 Case



A 27-year-old female with a history of systemic lupus erythematosus (SLE) was referred for evaluation of unilateral macular drusen. Family history of familial drusen was negative. On examination, visual acuity was 20/25 in the right eye (OD) and 20/20 in the left eye (OS). Funduscopy OD revealed numerous (>80) yellowish temporal perifoveal lesions (A). Funduscopy OS was normal (B).

 What is Your Next Step?



Start the Age-Related Eye Disease Study (AREDS) vitaminsEnhanced depth imaging optical coherence tomography (EDI OCT)Fluorescein angiographyBevacizumab intravitreal injection.

Illustration – [Figure 1].

[INLINE:1]

 Findings



EDI OCT OD showed drusen-like deposits (DLDs) located between the retinal pigment epithelium and Bruch membrane, with the largest DLD measuring 232 μm in base and 89 μm in elevation (C). Macula OS was intact by EDI OCT (D). Further systemic work-up revealed no evidence of glomerulonephritis.

 Diagnosis: drusen Like Deposits in SLE.



 Correct Answer: B.



 Discussion



Ocular involvement in SLE can occur in up to 30% of patients.[1] Asymptomatic choroidal alteration and DLDs in patients with SLE glomerulonephritis were first described in 2011 by Baglio et al. using indocyanine green angiography.[2] Later in 2017, Invernizzi et al. documented presence of DLDs, with or without glomerulonephritis, however, they found that patients with glomerulonephritis demonstrated more DLDs per eye, larger DLDs, and DLDs involvement of >3 quadrants (all P < 0.03).[3] We advise patients with SLE to have a thorough dilated funduscopic examination. A screening EDI OCT should be considered in patients with SLE.

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

Nil.

Conflicts of interest

There are no conflicts of interest.

References

1Palejwala NV, Walia HS, Yeh S. Ocular manifestations of systemic lupus erythematosus: A review of the literature. Autoimmune Dis 2012;2012:290898.
2Baglio V, Gharbiya M, Balacco-Gabrieli C, Mascaro T, Gangemi C, Di Franco M, et al. Choroidopathy in patients with systemic lupus erythematosus with or without nephropathy. J Nephrol 2011;24:522-9.
3Invernizzi A, dell'Arti L, Leone G, Galimberti D, Garoli E, Moroni G, et al. Drusen-like deposits in young adults diagnosed with systemic lupus erythematosus. Am J Ophthalmol 2017;175:68-76.