Two-stage surgical treatment for a giant sellar psammomatoid juvenile ossifying fibroma: case report

Author:

Twitchell Spencer1,Karsy Michael1,Gozal Yair M.1,Davidson Christian2,Couldwell William T.1,Brockmeyer Douglas13

Affiliation:

1. Departments of Neurosurgery and

2. Pathology, University of Utah; and

3. Primary Children’s Hospital, Salt Lake City, Utah

Abstract

Psammomatoid juvenile ossifying fibroma (PJOF) is an uncommon, benign fibro-osseous tumor. It is a purely surgical disease, and a review of the literature revealed that adjuvant therapies, including chemotherapy and radiation, play a limited role. The authors report the case of a 16-year-old male refugee who presented with a giant sinonasal PJOF with parasellar invasion, after having been unable to undergo earlier surgical treatment. The delay in presentation resulted in a large lesion with bilateral optic nerve compression, blindness, and frontal lobe compression. The patient was surgically treated with a two-stage combined cranial and endoscopic endonasal surgical approach. The delay in treatment and significant neurological compromise, which necessitated a two-stage approach, are unique from previously reported cases of PJOF.

Publisher

Journal of Neurosurgery Publishing Group (JNSPG)

Subject

General Medicine

Reference32 articles.

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