4.5 Review

Clinical characteristics and risk factors for bilateral lateral geniculate body pathology: a systematic review of the literature

Journal

NEUROLOGICAL SCIENCES
Volume -, Issue -, Pages -

Publisher

SPRINGER-VERLAG ITALIA SRL
DOI: 10.1007/s10072-023-06818-5

Keywords

Bilateral lateral geniculate body; Lateral geniculate nucleus; Bilateral vision loss; Mammillary body; Hemorrhagic infarct; Acute pancreatitis; Purtscher-like retinopathy

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This article presents a case report of a 17-year-old female with acute pancreatitis who developed acute onset bilateral painless vision loss due to bilateral infarction of the lateral geniculate bodies (LGB), and a systematic review of relevant literature. The review findings indicate that bilateral LGB infarction is a rare cause of vision loss, predominantly affecting women and often associated with systemic diseases.
BackgroundCase presentation of acute onset bilateral painless vision loss caused by bilateral infarction of the lateral geniculate bodies (LGB) and a systematic review of the literature.MethodsA descriptive case report is presented on a 17-year-old female diagnosed with acute pancreatitis who developed acute onset bilateral painless vision loss. A systematic literature review of cases with bilateral LGB lesions was conducted across three electronic databases (PubMed/PubMed Central/MEDLINE, Scopus, and ScienceDirect). The review was conducted in concordance with PRISMA guidelines and prospectively registered on PROSPERO (CRD42022362491).ResultsThe reported 17-year-old female was found to have MRI findings consistent with bilateral hemorrhagic infarction of the LGB and Purtscher-like retinopathy. A systematic literature review of bilateral LGB infarction yielded 23 records for analysis. 19/23 (82.6%) of reported cases occurred in women. Bilateral vision loss was noted in all cases. The average reported age was 27 years old with a range from 2-50. Gastrointestinal pathology (e.g., pancreatitis, gastroenteritis) was present in 8/23 (34.7%) of cases. 8/23 (34.7%) cases had neuroimaging or pathological evidence of hemorrhagic transformation of the infarct. Most cases experienced partial recovery of visual loss; only one case (4.7%) had complete visual recovery. 9/23 (39.1%) cases were reported from the United States and 4/23 (17.3%) from India.ConclusionsBilateral LGB lesion is a rare cause of vision loss, typically caused by systemic diseases and with female preponderance. Purported pathophysiology relates to increased vulnerability of the LGB to ischemic and metabolic stress.

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