| Literature DB >> 26900044 |
C Burgueño-Montañés1, C Santalla-Castro2, J Peña-Suárez3.
Abstract
CLINICAL CASE: A 33-year-old male diagnosed with Parinaud's syndrome, exotropia and post-papillary oedema optic atrophy in his left eye. A pineal germinoma was diagnosed after performing neuroimaging scans and a stereotactic biopsy. He was treated with chemotherapy and radiotherapy, showing a complete pathological response. The Parinaud's syndrome persists one year after diagnosis and the patient has refused to have strabismus surgery. DISCUSSION: Parinaud's syndrome consists of a supranuclear vertical gaze palsy resulting from damage to the midbrain tectum. The involvement of adjacent structures leads to the «Parinaud-plus» syndrome. When a Parinaud's syndrome is accompanied by diplopia («Parinaud-plus» syndrome), extension of the injury into adjacent areas must be considered.Entities:
Keywords: Disgerminoma; Dorsal midbrain syndrome; Dysgerminoma; Germinoma; Parinaud's syndrome; Pineal tumours; Síndrome de Parinaud; Síndrome mesencefálico dorsal; Tumores pineales
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Year: 2016 PMID: 26900044 DOI: 10.1016/j.oftal.2016.01.003
Source DB: PubMed Journal: Arch Soc Esp Oftalmol ISSN: 0365-6691