Surg Neurol Int. 2025;16:82.
A 33-year-old female with severe headaches and vertigo was diagnosed with cerebellar hemorrhage due to an isolated developmental venous anomaly (DVA). Conservative treatment led to full recovery, highlighting the importance of considering DVA in cerebellar hemorrhage etiology and recommending non-surgical management to avoid complications.
• Case Report: Idiopathic cerebellar hemorrhage with isolated developmental venous anomaly in a 33-year-old female.
• Symptoms: Severe headaches, vertigo, left oculomotor nerve palsy, left-sided hemidysmetria.
• Initial Misdiagnosis: Meniere’s disease.
• Imaging Findings: Acute hemorrhage in cerebellar vermis, isolated DVA with “caput medusae” sign.
• Management: Conservative treatment with steroids and analgesics, full recovery.
• DVA Characteristics: Benign anatomical variation, low-flow malformation, rarely causes hemorrhage.
• Hemorrhage Risk Factors: Coexisting cavernous malformation or arteriovenous malformation increase risk.
• Study Findings: Hemorrhage risk 0.22–0.68%/year, higher in infratentorial DVAs.
• Surgical Intervention: Reserved for life-threatening mass effects or raised intracranial pressure.


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