Fibrin-Heparin-Coated Intracranial Stents as Salvage Therapy in Pediatric Focal Cerebral Arteriopathy-Inflammatory

Marija Cagalj1, Anna Schaper1, Christian Brickmann2,3

  • 1Department of Diagnostic and Interventional Radiology and Neuroradiology (M.C., A.S., M.K., T.W.-D., A.M.), München Klinik Harlaching, München Klinik gGmbH, Munich, Germany.

Insights

Pediatric arterial ischemic stroke (AIS) in a 13-year-old boy with focal cerebral arteriopathy of inflammatory type (FCA-i) improved with endovascular therapy. Successful revascularization was achieved using angioplasty and stenting after medical treatments failed.

Area of Science:

  • Neurology
  • Pediatric Neurology
  • Vascular Neurology

Background:

  • Pediatric arterial ischemic stroke (AIS) is often linked to underlying arteriopathies.
  • Focal cerebral arteriopathy of inflammatory type (FCA-i) is a rare cause of AIS in children.
  • Progressive neurological deficits can occur despite standard medical management.

Purpose of the Study:

  • To report a case of progressive AIS in a pediatric patient due to FCA-i.
  • To evaluate the efficacy of endovascular therapy in managing this condition.
  • To highlight diagnostic findings including vessel wall MRI and serological markers.

Main Methods:

  • A 13-year-old male with progressive AIS underwent comprehensive medical therapy including antiplatelet agents, immunosuppressants, and antimicrobial treatment.
  • Intra-arterial spasmolysis was administered due to vasospasm.
  • Endovascular therapy involving balloon angioplasty and fibrin-heparin-coated intracranial stent placement was performed.
  • Diagnosis was supported by vessel wall MRI and elevated Mycoplasma pneumoniae antibodies.

Main Results:

  • The patient experienced clinical and radiographic deterioration despite initial medical treatments.
  • Endovascular therapy resulted in successful revascularization and clinical stabilization.
  • Vessel wall MRI and serological evidence confirmed FCA-i.
  • Sustained stent patency and vascular improvement were observed at follow-up.
  • Persistent distal upper-extremity-predominant hemiparesis remained.

Conclusions:

  • Endovascular therapy can be a viable treatment option for pediatric AIS secondary to FCA-i when medical management fails.
  • Vessel wall imaging and specific antibody testing are crucial for diagnosing FCA-i.
  • While endovascular treatment can stabilize the condition, long-term neurological deficits may persist.

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