Case reports in neurology · 2026
Prosopometamorphopsia as an Unusual Presentation of Cerebral Venous Sinus Thrombosis in a 33-Year-Old Filipino: A Case Report.
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Azurin Ronn Victor L, Bitanga Ester S
Аннотация
INTRODUCTION: Prosopometamorphopsia is a rare disorder of facial distortion that can be caused by cerebral infarcts, seizures, migraines, or trauma. In the most recent review of literature, there are no published reports for prosopometamorphopsia in cerebral venous sinus thrombosis (CVST).
CASE PRESENTATION: We discuss the case of a 33-year-old female who presented with acute-onset visual facial distortions. Cranial magnetic resonance imaging with contrast revealed venous sinus thrombosis involving the mid-to-caudal superior sagittal sinus, some of the bilateral parietal cortical veins, torcular Herophili, right transverse sinus, right sigmoid sinus, and right upper internal jugular vein without cerebral edema and hemorrhage. Optic disc photography revealed papilledema consistent with increased intracranial pressure. Blood work results were unremarkable. The patient was diagnosed in a timely manner and started on low-molecular-weight heparin (enoxaparin 1 mg/kg every 12 h) upon admission. She was discharged after 3 days of hospitalization, clinically improved and asymptomatic, on dabigatran 150 mg twice daily.
CONCLUSION: Prosopometamorphopsia is a rare phenomenon that should be recognized as an initial and unusual presentation of CVST. Timely neuroimaging and anticoagulation can lead to rapid resolution of symptoms and favorable outcomes.
CASE PRESENTATION: We discuss the case of a 33-year-old female who presented with acute-onset visual facial distortions. Cranial magnetic resonance imaging with contrast revealed venous sinus thrombosis involving the mid-to-caudal superior sagittal sinus, some of the bilateral parietal cortical veins, torcular Herophili, right transverse sinus, right sigmoid sinus, and right upper internal jugular vein without cerebral edema and hemorrhage. Optic disc photography revealed papilledema consistent with increased intracranial pressure. Blood work results were unremarkable. The patient was diagnosed in a timely manner and started on low-molecular-weight heparin (enoxaparin 1 mg/kg every 12 h) upon admission. She was discharged after 3 days of hospitalization, clinically improved and asymptomatic, on dabigatran 150 mg twice daily.
CONCLUSION: Prosopometamorphopsia is a rare phenomenon that should be recognized as an initial and unusual presentation of CVST. Timely neuroimaging and anticoagulation can lead to rapid resolution of symptoms and favorable outcomes.