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Published on: June 18, 2021
Aspirin-associated intracerebral hemorrhage in a patient with CADASIL
Jung-Hwan Oh1, Jung Seok Lee, Sa-Yoon Kang
1Department of Neurology, Cheju National University School of Medicine, Jeju, Republic of Korea.
Insights
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) patients may face intracerebral hemorrhage (ICH) risk, especially with hypertension and aspirin use. This case highlights potential links between microbleeds, antithrombotics, and ICH in CADASIL.
Area of Science:
- Neurology
- Vascular Neurology
- Genetics
Background:
- Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is a rare genetic disorder affecting small blood vessels in the brain.
- It typically presents with ischemic strokes, cognitive decline, and mood disturbances.
- Intracerebral hemorrhage (ICH) is an uncommon but recognized complication, with its etiology in CADASIL remaining unclear.
Observation:
- A 39-year-old male with a history of untreated hypertension and diagnosed CADASIL developed acute ICH.
- The hemorrhage occurred two weeks after initiating aspirin therapy.
- Brain imaging revealed a hyperacute ICH in the left temporal lobe, adjacent to a prior hemorrhage site, and evidence of cerebral microbleeds.
Findings:
- The case suggests a potential association between aspirin use, cerebral microbleeds, and the development of ICH in patients with CADASIL.
- The patient's history of hypertension is a significant contributing factor to vascular disease severity.
- Recurrent hemorrhage at a previous site indicates compromised vascular integrity.
Implications:
- This case underscores the need for careful consideration of antithrombotic therapy in CADASIL patients, particularly those with uncontrolled hypertension and evidence of microbleeds.
- Further research is warranted to elucidate the mechanisms linking CADASIL, microbleeds, and ICH to guide clinical management and risk stratification.
- Enhanced vigilance for hemorrhagic complications may be necessary in this patient population.
Abstract:
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is a hereditary disease characterized by ischemic stroke, cognitive impairment, migraine and neuropsychological deficit. Although intracerebral hemorrhage (ICH) has been described in patients with CADASIL, the cause of such ICH is still unknown. We present a 39-year-old man with CADASIL who had two years history of untreated hypertension. In this patient, acute ICH developed only two weeks after the initiation of aspirin. Brain images demonstrated a 3cmx3cm hyperacute ICH in the left temporal lobe at the site of previous old hemorrhage. The presence of cerebral microbleed and use of antithrombotics may be associated with development of ICH in patients with CADASIL.
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