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Unraveling the Puzzle: A Case Report Questioning the Causal Relationship Between Subarachnoid Hemorrhage and
Ashbina Pokharel1, Indira Acharya2, Joseph Skender3
1Internal Medicine, Beaumont Hospital, Royal Oak, USA.
Abstract:
Antineutrophil cytoplasmic antibody (ANCA)-associated vasculitides (AAV) are small-to-medium-vessel vasculitis, which includes granulomatosis with polyangiitis, microscopic polyangiitis (MPA), and eosinophilic granulomatosis with polyangiitis. MPA predominantly affects the kidneys and lungs. Subarachnoid hemorrhage (SAH), a life-threatening condition, rarely occurs with AAV. In this case, we present a 67-year-old female who presented with a sudden-onset headache after a recent diagnosis of ANCA-associated renal vasculitis. Kidney biopsy revealed pauci-immune glomerulonephritis, and serum was positive for ANCA along with myeloperoxidase antibody. A computed tomography scan of the head revealed both SAH and intraparenchymal hemorrhage. The patient was managed medically for SAH and intraparenchymal hemorrhage. ANCA vasculitis was treated with steroids and rituximab, and the patient showed improvement.
Insights
A rare case of subarachnoid hemorrhage (SAH) occurred in a patient with microscopic polyangiitis (MPA), a type of ANCA-associated vasculitis. Prompt medical and immunosuppressive treatment led to patient improvement.
Area of Science:
- Nephrology
- Neurology
- Rheumatology
Background:
- Antineutrophil cytoplasmic antibody (ANCA)-associated vasculitides (AAV) are systemic autoimmune diseases affecting small-to-medium-sized blood vessels.
- Microscopic polyangiitis (MPA), a subtype of AAV, primarily impacts the kidneys and lungs.
- Subarachnoid hemorrhage (SAH) is a rare but severe neurological complication associated with AAV.
Observation:
- A 67-year-old female with newly diagnosed ANCA-associated renal vasculitis presented with sudden severe headache.
- Cerebral imaging revealed both subarachnoid hemorrhage (SAH) and intraparenchymal hemorrhage.
- Kidney biopsy confirmed pauci-immune glomerulonephritis with positive ANCA and myeloperoxidase antibodies.
Findings:
- The patient received medical management for the intracranial hemorrhages.
- Immunosuppressive therapy, including steroids and rituximab, was administered for the ANCA vasculitis.
- The patient demonstrated clinical improvement following treatment for both conditions.
Implications:
- This case highlights the rare but critical association between ANCA vasculitis and intracranial hemorrhage.
- Early diagnosis and multidisciplinary management are crucial for improving outcomes in patients with AAV and neurological complications.
- Further research may elucidate the specific mechanisms linking AAV to cerebrovascular events.
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