Atypical Terson syndrome after subarachnoid hemorrhage from middle cerebral artery aneurysm rupture during coitus

Author:

Marrone Salvatore1,Pizzo Corrado2,Paolini Federica3,Giovannini Evier Andrea3,Crea Antonio4,Cinquemani Giovanni1,Lipani Rita1,Ruggeri Luca1,Mandelli Jaime1,Iacopino Domenico Gerardo3,Bona Giuseppe2,Basile Luigi1

Affiliation:

1. Unit of Neurosurgery, S. Elia Hospital, Caltanissetta, Italy

2. Unit of Ophtalmology, S. Elia Hospital, Caltanissetta, Italy

3. Neurosurgical Clinic, AOUP “Paolo Giaccone”, Post Graduate Residency Program in Neurologic Surgery, Department of Biomedicine Neurosciences and Advanced Diagnostics, School of Medicine, University of Palermo, Palermo, Italy

4. Department of Neurosurgery, Highly Specialized Hospital of National Importance “Garibaldi”, Catania, Italy

Abstract

Background: Terson syndrome (TS) is a neuro-ophthalmologic disease arising due to subarachnoid hemorrhage (SAH), resulting in the formation of subhyaloid hemorrhagic spots. These spots can affect the ability to see due to the alteration of the optic cameras. Although it often affects both eyes, the symptoms and the eye involvement can be asymmetrical in rare cases. Case Description: We described the case of a 52-year-old female patient who developed Terson disease following the rupture of a right middle cerebral artery aneurysm occurring during coitus with SAH (Fisher grade III). The aneurysm was treated by endovascular coiling. Interestingly, despite the major involvement of the right eye, the patient primarily manifested symptoms of visual changes in the left eye. Conclusion: TS is a frequent ocular complication of SAH, with symptoms typically affecting both eyes. Characterized by hemorrhagic spots in both subhyaloid layers, the syndrome’s symptomatology is generally bilateral. However, in the case described, the manifestation is deemed atypical, primarily appearing contralateral to the hemisphere exhibiting a greater pattern of SAH.

Publisher

Scientific Scholar

Reference35 articles.

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