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A Case of Intracranial Invasion from Sinonasal Small Cell Neuroendocrine Carcinoma Yasuhiro ONO 1 , Yoshio HISAMATSU 1 , Satoshi KURAMOTO 1 , Atsushi KATSUMATA 1 , Masamitsu KAWAUCHI 1 , Kengo KANAI 2 , Satoko NAKAMURA 3 , Takanori HIROSE 4 1Department of Neurosurgery, Kagawa Prefectural Central Hospital 2Department of Otolaryngology, Kagawa Prefectural Central Hospital 3Department of Pathology, Kagawa Prefectural Central Hospital 4Department of Diagnostic Pathology, Tokushima Prefectural Central Hospital Keyword: neuroendocrine carcinoma , intracranial invasion , diagnosis and treatment pp.453-459
Published Date 2014/5/10
DOI https://doi.org/10.11477/mf.1436102241
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 Sinonasal neuroendocrine carcinomas(NECs)are rare tumors. We present a rare case of intracranial invasion of sinonasal small-cell NEC. A 61-year-old woman with nasal obstruction and bleeding was referred to our hospital. Computed tomography showed a polyp-like tumor occupying her left nasal cavity and extending to the paranasal sinuses and anterior cranial fossa. The tumor was removed using a transfacial approach by otolaryngologists and a bifrontal cranial approach by neurosurgeons. In histopathological analyses, we found that the tumor presented with both an epithelial and neuroendocrine nature, and was diagnosed as a small-cell NEC. Post-surgery, she received localized radiation therapy and chemotherapy, and is alive, 18 months after diagnosis. In cases where it is difficult to perform a differential diagnosis of tumors arising from the frontal cranial base and extending to the nasal and cranial sides, NEC should be considered as a possibility.


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電子版ISSN 1882-1251 印刷版ISSN 0301-2603 医学書院

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