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DOI 10.1186/s13256-025-05101-9

Медицинская библиотека · Journal of medical case reports · 2025

Multiple evanescent white dot syndrome masquerading as atypical optic neuritis: a case report.

Han Kwang Eon, Lee Seung Min, Kim Su-Jin, Choi Heeyoung, Choi Jae Hwan

СтатьяКлинический случайПеревод в очереди

Аннотация

BACKGROUND

Multiple evanescent white dot syndrome is a rare posterior uveitis that presents with transient white dots in the retina, which may not always be visible at the time of diagnosis. The disease can mimic atypical optic neuritis owing to overlapping symptoms such as central visual field defect, relative afferent pupillary defect, and optic disc swelling. Here, we report a case of multiple evanescent white dot syndrome masquerading as atypical optic neuritis in a young female patient.

CASE PRESENTATION: A 23-year-old female patient of Korean ethnicity presented with ocular pain and visual field defect in her left eye for 1 week. Her best corrected visual acuity was 20/20 in her right eye and 20/30 in her left eye. Pupillary size was 3 mm for both eyes. Relative afferent pupillary defect was detected in the left eye. The color vision test was normal for both eyes. A visual field test revealed blind spot enlargement in the left eye. On fundus examination, disc swelling was found in the left eye. Other abnormalities were not found. The patient was suspected of having atypical optic neuritis. Fluorescein angiography showed hyperfluorescent spots in the posterior pole and leakage from the disc in the left eye. Orbital magnetic resonance imaging did not show any abnormal findings or enhancement. A multifocal electroretinogram showed reduced amplitude for the involved area. There were relatively hyperautofluorescent lesions outside the fovea and hypoautofluorescent fovea on the blue-light fundus autofluorescence image. En face optical coherence tomography revealed multiple hyporeflective dots at the ellipsoid zone. Swept-source optical coherence tomography showed irregular cells in the ellipsoid zone with increased outer retinal thickness. On repeated fundus examination, multiple white dots were found (vaguely). The patient was diagnosed with multiple evanescent white dot syndrome and was able to recover in 6 weeks.

CONCLUSION

Patients with multiple evanescent white dot syndrome who present with disc swelling, ocular pain, and relative afferent pupillary defect might be misdiagnosed as having optic neuritis. In atypical optic neuritis, en face optical coherence tomography, blue-light fundus autofluorescence, and swept-source optical coherence tomography can aid in the differential diagnosis.

Для цитирования: Han Kwang Eon, Lee Seung Min, Kim Su-Jin, Choi Heeyoung, Choi Jae Hwan. Multiple evanescent white dot syndrome masquerading as atypical optic neuritis: a case report.. Journal of medical case reports. 2025. DOI: 10.1186/s13256-025-05101-9.

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