Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5634970 | World Neurosurgery | 2017 | 24 Pages |
Abstract
Multiple CPA tumors are rare, heterogeneous lesions with a marked predisposition toward poor facial nerve outcomes, potentially attributable to a paracrine mechanism that simultaneously drives multiple tumor growth and increases invasiveness or adhesiveness at the facial nerve-tumor interface. Preceding nomenclature has been confounding and inconsistent; we recommend classifying all multiple CPA tumors as “synchronous tumors,” with “schwannoma with meningothelial hyperplasia” or “tumor-to-tumor metastases” reserved for rare, specific circumstances.
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Authors
Christopher S. Graffeo, Avital Perry, William R. III, Caterina Giannini, Brian A. Neff, Colin L.W. Driscoll, Michael J. Link,