An Unusual Case of Unilateral Papilledema

Author Affiliation
Daniel Quesada, MD Kern Medical Center, Department of Emergency Medicine, Bakersfield, California;
LA+USC Medical Center, Department of Emergency Medicine, Los Angeles, California
Matthew Stapleton, MD Kern Medical Center, Department of Emergency Medicine, Bakersfield, California
Jadipak Heer, MD Kern Medical Center, Department of Emergency Medicine, Bakersfield, California
Phillip Aguìñiga-Navarrete, RA Kern Medical Center, Department of Emergency Medicine, Bakersfield, California
Luke Kim, RA Kern Medical Center, Department of Emergency Medicine, Bakersfield, California

Case presentation
Discussion

ABSTRACT

 

Neuroretinitis from neurosyphilis is an uncommon finding in previously healthy young individuals. A 37-year-old presented with three days of painless, unilateral vision loss with an associated diffuse erythematous non-pruritic truncal rash. Physical exam demonstrated vision loss in the left eye. Fundoscopic exam showed unilateral peripapillary hemorrhage, papilledema and venous engorgement. Labs showed positive syphilis antibody qualitative. Magnetic resonance imaging demonstrated 12 millimeters of high right frontal lobe cerebrospinal fluid density. The patient was treated with benzylpenicillin and within 18 hours had improvement of his vision.

CASE PRESENTATION

A 37-year-old male presented to the emergency department complaining of three days of painless left eye vision changes. He described the changes as a “white out.” He also noted a four-week-old diffuse, erythematous, nonpruritic truncal rash. Visual exam findings were notable for oculus sinister of 20/25. Oculus dexter was 20/20. There was no presence of ptosis. Bilateral fluorescein stain and slit lamp exam were unremarkable. A fundoscopic exam of the left eye revealed unilateral papilledema (UP) and bilateral retinal hemorrhage (Image 1). Ocular pressures were unremarkable.

 

Image 1
Fundoscopic findings revealing peripapillary hemorrhage (white arrow), papilledema (dashed arrow), and venous engorgement (arrowhead).

Labs were significant for reactive hepatitis B, antinuclear antibody screen, rapid plasma reagin test with reflex, fluorescent treponemal antibody absorption test, sedimentation rate Westergren automated test, and c-reactive protein of 3.1 milligrams per deciliter (mg/dL) (0.0–3.1 mg/dL). Venereal disease research laboratory on cerebrospinal fluid (CSF) was nonreactive. Lyme antibody screen and Bartonella antibody panel were both negative. Syphilis antibody qualitative was positive. Rapid human immunodeficiency virus (HIV) test was negative. Syphilitic and UP findings prompted a lumbar puncture to rule out neurosyphilis, which subsequently revealed elevated lymphocytes 100% (40–80%) and protein 65.0 mg/dL (15.0–45.0 mg/dL).

A magnetic resonance imaging of the brain revealed 12 millimeters of high right frontal lobe CSF density (Image 2). The patient was given benzylpenicillin with subsequent vision improvement within 18 hours of administration, indicative of painless vision loss secondary to neurosyphilitic neuroretinitis.

 

Image 2
Magnetic resonance image of the brain revealing 12-millimeter right frontal lobe cerebrospinal fluid density (arrow).

DISCUSSION

Common causes of UP and vision loss include anterior ischemic optic neuropathy (AION) and optic neuritis (ON).1 AION is often seen in patients older than 50 years with associated comorbidities, making it an unlikely cause of this patient’s vision loss.1 ON typically affects females between 20–35 years of age.1 ON in 90% of cases has associated headaches, eye pain or both, whereas 19% of AION cases have associated pain.1 Neuroretinitis is uncommon, typically characterized by optic disc edema and subsequent formation of a macular star figure. The underlying pathophysiology involves increased permeability of disc vasculature, but is not fully defined.2

Our patient’s exam and symptoms were most consistent with neuroretinitis. Most cases of neuroretinitis are reported in ophthalmology literature and in association with cat scratch disease (CSD). Only about 1% of the 12,000 yearly cases of CSD present with neuroretinitis. Those who have reported cases of ophthalmological complaints not neuroretinitis specifically are individuals who are HIV positive.3 Our specific case demonstrates an uncommon presentation of unilateral papilledema in a healthy patient. Painless unilateral papilledema in younger patients should raise concern for an insidious process and prompt thorough investigation.

 

CPC-EM Capsule

What do we already know about this clinical entity?

Neuroretinitis is most commonly found in patients with cat scratch disease.

What is the major impact of the image(s)?

This case demonstrates a rare presentation of unilateral papilledema in an otherwise healthy patient.

How might this improve emergency medicine practice?

Unilateral papilledema in younger populations presenting without pain should prompt a thorough medical and physical examination with a widened differential diagnosis.

 

Footnotes

Section Editors: Christopher Sampson, MD

Full text available through open access at http://escholarship.org/uc/uciem_cpcem

Documented patient informed consent and/or Institutional Review Board approval has been obtained and filed for publication of this case report.

Address for Correspondence: Daniel Quesada, MD, Kern Medical Center, Department of Emergency Medicine, 1700 Mount Vernon Ave., Bakersfield, CA 93306. Email: daniel.quesada@kernmedical.com. 3:444 – 445

Submission history: Revision received May 1, 2019; Submitted July 25, 2019; Accepted August 2, 2019

Conflicts of Interest: By the CPC-EM article submission agreement, all authors are required to disclose all affiliations, funding sources and financial or management relationships that could be perceived as potential sources of bias. The authors disclosed none.

REFERENCES

1. Hata M, Miyamoto K. Causes and prognosis of unilateral and bilateral optic disc swelling. Neuroophthalmology. 2017;41(4):187-91.

2. Ghauri RR, Lee AG. Optic disk edema with a macular star. Surv Ophthalmol. 1998;43(3):270-4.

3. Purvin V, Sundaram S, Kawasaki A. Neuroretinitis: review of the literature and new observations. J Neuroophthalmol. 2011;31(1):58-68.