Subependymoma and dysembryoplastic neuroepithelial collision tumor in the foramen of Monro: case report

Author:

D’Agostino Erin1,Calnan Daniel R.2,Hickey William13,Bauer David F.12

Affiliation:

1. Geisel School of Medicine, Dartmouth College, Hanover; and

2. Section of Neurosurgery, Department of Surgery, Dartmouth-Hitchcock Medical Center, and

3. Department of Pathology, Dartmouth-Hitchcock Medical Center, Lebanon, New Hampshire

Abstract

Intracranial collision tumors have rarely been reported in the literature and generally include at least 1 malignant tumor component. Subependymoma with dysembryoplastic neuroepithelial tumor (DNET) is an as-yet unreported combination. Both components are uncommon tumors, and presentation in the foramen of Monro is even more unusual. A 16-year-old male patient with a past medical history significant for asthma presented with a 3-month history of headaches and radiographic evidence of mild obstructive hydrocephalus secondary to a nonenhancing ventricular lesion at the foramen of Monro. He underwent endoscopic biopsy and resection. Pathological analysis revealed distinct components of subependymoma and DNET. At the 1-year follow-up, the patient was doing well without regrowth of tumor. The authors describe a case of intracranial collision tumor demonstrating 2 grade I components: a novel combination of subependymoma and DNET.

Publisher

Journal of Neurosurgery Publishing Group (JNSPG)

Subject

General Medicine

Reference54 articles.

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5. The usefulness of MR imaging in the diagnosis of dysembryoplastic neuroepithelial tumor in children: a study of 14 cases;Fernandez;AJNR Am J Neuroradiol,2003

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