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Ocular Pathologic Findings of Neurofibromatosis Type 2
Margaret E. McLaughlin, MD;
Susan M. Pepin, MD;
Mia MacCollin, MD;
Pitipol Choopong, MD;
Simmons Lessell, MD
Arch Ophthalmol. 2007;125(3):389-394.
Objective To gain insight into the pathogenesis of neurofibromatosis type 2 (NF2) by investigating the ocular manifestations of this disease.
Methods Using standard histologic techniques, immunohistochemistry, and electron microscopy, we described the ocular pathologic findings of a 34-year-old woman who died from complications of NF2.
Results We identified 3 types of NF2-associated lesions: juvenile posterior subcapsular cataracts, epiretinal membranes, and an intrascleral schwannoma.
Conclusions Our analysis indicated that dysplastic lens cells accumulate just anterior to the posterior lens capsule in juvenile posterior subcapsular cataracts and that dysplastic Müller cells may be a major component of NF2-associated epiretinal membranes.
Clinical Relevance Our findings suggest that a subset of glial cells with epithelial features (Schwann cells, ependymal cells, and Müller cells) may be particularly sensitive to loss of the NF2 gene. Understanding the molecular basis for this sensitivity may lead to novel strategies for treating NF2.
Author Affiliations: Department of Biology and Center for Cancer Research, Massachusetts Institute of Technology, Cambridge (Dr McLaughlin); and Department of Pathology, Brigham and Women's Hospital (Dr McLaughlin), Department of Ophthalmology, Massachusetts Eye and Ear Infirmary (Drs Pepin, Choopong, and Lessell), and Department of Neurology, Massachusetts General Hospital (Dr MacCollin), Boston.
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