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Volume 51, Issue 2, Pages 162-168 (March 2006)


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Plexiform Pigmented Schwannoma of the Uvea

Egbert Saavedra, MD1, Arun D. Singh, MD1Corresponding Author Information, Jonathan E. Sears, MD1, Norman B. Ratliff, MD2

Abstract 

Schwannoma is a slow growing solitary tumor that preferentially involves spinal nerve roots, and sympathetic, cervical, and vagus nerves. There are several clinico-pathologic variants of schwannoma, including schwannoma with a degenerative change (ancient schwannoma), cellular schwannoma, plexiform schwannoma, epithelioid schwannoma, and melanotic schwannoma. About 10% of cases of schwannomas are associated with multi-system disorders such as neurofibromatosis, schwannomatosis, multiple meningiomas, and Carney complex. Schwannoma rarely present as an intraocular tumor and is often misdiagnosed as malignant melanoma. Immunohistochemical positivity with S-100 stain and demonstration of long-spaced collagen (Luse bodies) are helpful in establishing the diagnosis. In this article, we review the clinical and histopathological findings of a sporadic plexiform pigmented schwannoma involving the iris, ciliary body, and the choroid.

STEFAN SEREGARD AND MILTON BONIUK, EDITORS

1 Cole Eye Institute

2 Department of Pathology, Cleveland Clinic Foundation, Cleveland, Ohio, USA

Corresponding Author InformationReprint address: Arun D. Singh, MD, Department of Ophthalmic Oncology, Cole Eye Institute (i3-129), Cleveland Clinic Foundation, 9500 Euclid Avenue, Cleveland, Ohio 44195.

 The authors reported no proprietary or commercial interest in any products mentioned or concepts discussed in this article.

PII: S0039-6257(05)00209-2

doi:10.1016/j.survophthal.2005.12.004


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