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Multiple Plexiform Schwannomas Associated with Neurofibromatosis Type 2: A case report.
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HOME > J Pathol Transl Med > Volume 34(5); 2000 > Article
Case Report Multiple Plexiform Schwannomas Associated with Neurofibromatosis Type 2: A case report.
Ho Sung Park, Myoung Ja Chung, Myoung Jae Kang, Dong Geun Lee, Byung Cook Ahn
Journal of Pathology and Translational Medicine 2000;34(5):389-392
DOI: https://doi.org/
1Departments of Pathology, Chonbuk National University Medical School, Chonju 561-180, Korea.
2Departments of Ophthalmology, Chonbuk National University Medical School, Chonju 561-180, Korea.
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Plexiform schwannoma is a rare benign tumor arising from the peripheral nerve sheath and characterized by a multinodular and plexiform growth pattern. This tumor usually arises sporadically. In rare cases, plexiform schwannomas have been associated with neurofibromatosis type 2. Plexiform schwannoma should be differentiated from plexiform neurofibroma, because the latter is pathognomonic tumor of neurofibromatosis type 1 and has a potential of malignant transformation. We report a case of multiple plexiform schwannomas associated with bilateral acoustic neuromas and meningioma.

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