Acute bilateral multiple subcortical infarcts as manifestation in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy

Neurol Sci. 2023 Dec;44(12):4391-4399. doi: 10.1007/s10072-023-06949-9. Epub 2023 Jul 17.

Abstract

Background: Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is characterised by recurrent subcortical ischemic events, migraine with aura, dementia and mood disturbance. Strokes are typically lacunar infarcts; however, bilateral multiple subcortical lacunar infarcts have been described only sporadically.

Method: We described four CADASIL patients who presented with acute bilateral multiple subcortical infarcts as the first manifestation. We also briefly summarised the case reports detailing the bilateral multiple infarcts in CADASIL.

Results: Patient 1 and patient 2 were family members, and they presented with cognitive impairment. Patient 3 and patient 4 presented with slurred speech and hemiparesis. Patients 1, 3 and 4 developed hemodynamic fluctuations before the occurrence of ischemic stroke. Laboratory tests revealed elevated fibrinogen levels in patients 3 and 4. The brain magnetic resonance imaging showed acute bilateral multiple subcortical infarcts on the periventricular white matter in all the patients.

Conclusion: CADASIL, with a poor brain hemodynamic reserve, is vulnerable to hemodynamic alterations (e.g. blood pressure fluctuation, dehydration, blood loss and anaemia) and intolerable to ischemia and hypoxia of the brain. Furthermore, blood hypercoagulation may contribute to acute multiple bilateral infarctions in CADASIL. Therefore, it is necessary to avert these predispositions in CADASIL patients in their daily life.

Keywords: CADASIL; Multiple infarcts; NOTCH3; Stroke.

MeSH terms

  • Brain / diagnostic imaging
  • Brain / pathology
  • CADASIL* / complications
  • CADASIL* / diagnostic imaging
  • CADASIL* / pathology
  • Humans
  • Leukoencephalopathies* / diagnostic imaging
  • Leukoencephalopathies* / etiology
  • Leukoencephalopathies* / pathology
  • Magnetic Resonance Imaging
  • Migraine Disorders* / pathology
  • Receptor, Notch3 / genetics
  • Stroke, Lacunar* / pathology

Substances

  • Receptor, Notch3