Amyloid-Beta related angiitis of the central nervous system: case report and topic review

Amre Nouh1, Ewa Borys2, Angelica K Gierut3

  • 1Department of Neurology, Stritch School of Medicine, Loyola University Chicago , Maywood, IL , USA.

Frontiers in Neurology
|February 20, 2014
PubMed

Insights

Amyloid-beta related angiitis (ABRA) is a rare central nervous system (CNS) disorder. This case study details a patient diagnosed with ABRA, highlighting its overlapping features with other CNS conditions.

Area of Science:

  • Neurology
  • Neuroimmunology
  • Vascular Neurology

Background:

  • Amyloid-beta related angiitis (ABRA) is a rare neurological disorder.
  • It presents with overlapping clinical and radiological features of primary angiitis of the CNS and cerebral amyloid angiopathy.
  • ABRA affects the central nervous system (CNS).

Purpose of the Study:

  • To describe a case of ABRA in a 74-year-old male patient.
  • To discuss the clinicopathological features of ABRA.
  • To review the existing literature on ABRA.

Main Methods:

  • Case report of a 74-year-old male with intermittent left-sided weakness.
  • Magnetic Resonance Imaging (MRI) findings including leptomeningeal enhancement, vasogenic edema, and subcortical white matter disease.
  • Pathological confirmation of ABRA.

Main Results:

  • The patient presented with neurological deficits and characteristic MRI findings.
  • Diagnosis of ABRA was confirmed.
  • The case illustrates the complex presentation of ABRA.

Conclusions:

  • ABRA is a rare CNS vasculopathy with features mimicking other conditions.
  • Early recognition and diagnosis are crucial for appropriate management.
  • Further research is needed to understand ABRA pathogenesis and treatment.