Juvenile Pilocytic Astrocytoma in Association with Arteriovenous Malformation

Author:

Soltanolkotabi M.1,Schoeneman S.E.2,Dipatri A.J.3,Hurley M.C.1,Ansari S.A.1,Rajaram V.4,Tomita T.3,Shaibani A.12

Affiliation:

1. Department of Radiology, Northwestern University Feinberg School of Medicine; Chicago, IL, USA

2. Department of Medical Imaging, Anne & Robert H. Lurie, Children's Memorial Hospital of Chicago; Chicago, IL, USA

3. Department of Neurosurgery, Anne & Robert H. Lurie, Children's Memorial Hospital of Chicago; Chicago, IL, USA

4. Department of Pathology, Anne & Robert H. Lurie, Children's Memorial Hospital of Chicago; Chicago, IL, USA

Abstract

Pilocytic astrocytomas are highly vascular, relatively common primary brain tumors in the pediatric population, but their association with a true arteriovenous malformation (AVM) is extremely rare. We describe an eight-year-old girl with a right supratentorial juvenile pilocytic astrocytoma (WHO grade I) with an angiographically documented AVM entangled in the tumor mass who presented with intracranial hemorrhage due to a ruptured anterior choroidal artery pseudoaneurysm encased in the lesion. The AVM nidus as well as the hemorrhage site was embolized with Onyx. A literature review revealed only one previous report of a true intermixture of these two lesions. We hypothesize whether the association of vascular malformations and primary brain tumors are merely coincidental or if they point to the existence of a distinct entity and/or a common etiologic factor.

Publisher

SAGE Publications

Subject

Immunology

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