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Stereotactic radiosurgery for aggressive papillary tumor of the temporal bone: case report

BACKGROUND Papillary tumors of the temporal bone are very rare neoplasms that show locally aggressive behavior though they have low-grade histologic features. The best treatment for these tumors is a radical resection. However, if the tumor is very large, local invasiveness and hypervascularity can...

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Bibliographic Details
Published in:Surgical neurology 2002-08, Vol.58 (2), p.124-127
Main Authors: Kamida, Tohru, Isono, Mitsuo, Inoue, Ryo, Wakabayashi, Yukihiro, Goda, Makoto, Ishii, Keisuke, Kobayashi, Hidenori
Format: Article
Language:English
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Summary:BACKGROUND Papillary tumors of the temporal bone are very rare neoplasms that show locally aggressive behavior though they have low-grade histologic features. The best treatment for these tumors is a radical resection. However, if the tumor is very large, local invasiveness and hypervascularity can prevent surgeons from achieving a complete resection. As an additional treatment for the residual tumor, it remains controversial whether radiation therapy has any role. CASE DESCRIPTION The authors describe a 53-year-old woman who suffered from left-sided tinnitus, hearing loss, and diplopia due to a large aggressive papillary tumor of the temporal bone. Radiosurgery was very effective for the tumor, which had regrown a few years after conventional radiation therapy and chemotherapy. Conclusions The authors conclude that radiosurgery should be considered as an option for the treatment of aggressive papillary tumor of the temporal bone.
ISSN:0090-3019
1879-3339
DOI:10.1016/S0090-3019(02)00760-7