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Brain fog and vessel clogs.

Aditya Maitray1, Anju Kuriakose1, Anand Rajendran1

  • 1Department of Vitreo Retina Services, Aravind Eye Hospital, Chennai, Tamil Nadu, India.

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Summary
This summary is machine-generated.

A rare case of Susac syndrome (SS) in a 36-year-old female presented with vision loss, hearing impairment, and encephalopathy. This condition, marked by retinal vascular occlusion, required advanced multimodal imaging and treatment.

Keywords:
Bilateral CRAOSusac syndromecombined vascular occlusion

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Area of Science:

  • Ophthalmology
  • Neurology
  • Vascular Medicine

Background:

  • Susac syndrome (SS) is a rare autoimmune condition characterized by the triad of encephalopathy, branch retinal artery occlusions (BRAOs), and sensorineural hearing loss.
  • While typically affecting young women, SS can present with varied and sometimes atypical features, posing diagnostic challenges.

Observation:

  • A 36-year-old female presented with symptoms indicative of bilateral retinal vascular occlusion, hearing loss, and encephalopathy.
  • Comprehensive ocular examinations, including wide-field fundus photography, OCT, and FA, were performed.
  • Systemic investigations were conducted in conjunction with neurological and otological consultations.

Findings:

  • The patient was diagnosed with Susac syndrome (SS).
  • The case highlights a rare presentation of combined bilateral retinal vascular occlusion in the context of SS.
  • Treatment involved laser photocoagulation and pars plana vitrectomy.

Implications:

  • This case underscores the importance of considering SS in patients with the characteristic triad, even with atypical vascular findings.
  • Early diagnosis and multimodal treatment are crucial for managing SS and preventing vision and neurological deficits.
  • Further research into the pathogenesis and optimal management strategies for rare SS variants is warranted.