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Double Direct Injection of Blood into the Cisterna Magna as a Model of Subarachnoid Hemorrhage
Published on: August 30, 2020
Subarachnoid hemorrhage caused by ruptured intracranial fusiform aneurysm associated with microscopic polyangiitis
Hidehito Kimura1, Nobuyuki Akutsu, Ryoji Shiomi
1Department of Neurosurgery, Toyooka Public Hospital, Hyogo, Japan. hidekimura-nsu@umin.ac.jp
Abstract:
A 44-year-old woman with microscopic polyangiitis (MPA) presented with a ruptured cerebral aneurysm. She was admitted to our hospital for further examination of progressive renal failure. She was found lying on the ward floor. Computed tomography showed subarachnoid hemorrhage, and digital subtraction angiography revealed a saccular-like aneurysm arising from the right distal posterior inferior cerebellar artery (PICA) at the non-branching site. We performed neck clipping of the right distal PICA aneurysm, which recurred 5 days after the operation. Second angiography demonstrated a right distal PICA aneurysm just above the site of the clip. Therefore, we performed trapping of the affected lesion with emergent bypass of the contralateral occipital artery to the ipsilateral PICA. Her postoperative course was uneventful until she coughed up blood and had gross hematuria 3 days after the second surgery. Histological examination of a renal biopsy specimen revealed crescentic glomerulonephritis. MPA was diagnosed on the basis of the cardinal symptoms, including progressive glomerular nephritis and the lung abnormality, as well as the presence of myeloperoxidase-antineutrophil cytoplasmic antibodies. After intensive treatment, she was discharged for rehabilitation without neurological deficit. MPA commonly affects small-sized vessels mainly in the kidneys and lungs and may lead to crescentic glomerulonephritis and pulmonary hemorrhage. MPA is rarely associated with aneurysms of medium-sized muscular vessels. Cerebral aneurysm is extremely rare in patients with MPA, but rupture of an intracranial fusiform aneurysm can be lethal, so screening of the intracranial vessels should be performed by magnetic resonance imaging in patients with MPA.
Insights
Microscopic polyangiitis (MPA) can cause rare cerebral aneurysms. This case highlights MPA
Area of Science:
- Neurology
- Nephrology
- Rheumatology
Background:
- Microscopic polyangiitis (MPA) typically affects small vessels in the kidneys and lungs.
- Cerebral aneurysms are an extremely rare manifestation of MPA.
Observation:
- A 44-year-old woman with MPA presented with a ruptured cerebral aneurysm and progressive renal failure.
- Initial treatment for a posterior inferior cerebellar artery (PICA) aneurysm recurred, necessitating a second intervention with bypass.
- The patient subsequently developed crescentic glomerulonephritis and pulmonary hemorrhage, confirming MPA diagnosis.
Findings:
- Successful treatment of a recurrent PICA aneurysm with bypass and trapping.
- Histological confirmation of crescentic glomerulonephritis, a known complication of MPA.
- Patient discharged without neurological deficit after intensive treatment for MPA complications.
Implications:
- This case underscores the importance of considering rare vascular complications like cerebral aneurysms in MPA patients.
- Screening for intracranial aneurysms using magnetic resonance imaging is recommended for patients with MPA.
- Prompt diagnosis and management of MPA-related glomerulonephritis and hemorrhage are crucial for patient outcomes.
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