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Composite pheochromocytoma of the adrenal gland: a case series
http://hdl.handle.net/10069/35816
http://hdl.handle.net/10069/358164d1c2854-2c57-4782-a641-9571913e123a
名前 / ファイル | ライセンス | アクション |
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BMCRN8_257.pdf (2.0 MB)
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Item type | 学術雑誌論文 / Journal Article(1) | |||||
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公開日 | 2015-09-03 | |||||
タイトル | ||||||
タイトル | Composite pheochromocytoma of the adrenal gland: a case series | |||||
言語 | ||||||
言語 | eng | |||||
キーワード | ||||||
主題Scheme | Other | |||||
主題 | Adrenal gland | |||||
キーワード | ||||||
主題Scheme | Other | |||||
主題 | Composite pheochromocytoma | |||||
キーワード | ||||||
主題Scheme | Other | |||||
主題 | Ganglioneuroblastoma | |||||
キーワード | ||||||
主題Scheme | Other | |||||
主題 | Ganglioneuroma | |||||
キーワード | ||||||
主題Scheme | Other | |||||
主題 | Hemodialysis | |||||
キーワード | ||||||
主題Scheme | Other | |||||
主題 | Ki67 | |||||
資源タイプ | ||||||
資源タイプ識別子 | http://purl.org/coar/resource_type/c_6501 | |||||
資源タイプ | journal article | |||||
著者 |
Shida, Yohei
× Shida, Yohei× Igawa, Tsukasa× Abe, Kuniko× Hakariya, Tomoaki× Takehara, Kousuke× Onita, Toru× Sakai, Hideki |
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抄録 | ||||||
内容記述タイプ | Abstract | |||||
内容記述 | Background: Composite pheochromocytoma is a rare pathological condition characterized by elements of both pheochromocytoma and neurogenic tumors. However, detailed clinical outcomes of this tumor have not been fully shown. From 2007 to 2013, we experienced three cases of adrenal composite pheochromocytoma. In this report, we investigate the clinicopathological features of these three cases of composite pheochromocytoma and compare them with previously reported cases. Case presentations: Cases 1 and 2 were a 29-year-old Japanese woman and a 59-year-old Japanese man, respectively. They underwent laparoscopic left adrenalectomy, and pathological examination revealed composite pheochromocytoma-ganglioneuroma. Case 3 was a 53-year-old Japanese man who had been receiving hemodialysis for 17 years. He underwent laparoscopic right adrenalectomy, and pathological examination revealed composite pheochromocytoma-ganglioneuroblastoma. Although the Ki67-positive rates varied from 1.0 to 6.2% among the three cases, no clinical recurrences occurred. Despite the relatively high rate of Ki67 positivity, complete tumor resection resulted in favorable clinical outcomes. Conclusion: We experienced three cases of adrenal composite pheochromocytoma. Although the clinical findings and treatment outcomes of composite pheochromocytoma were similar to those of ordinary pheochromocytoma, further studies of the biological behavior and genetic profiles of composite pheochromocytoma are necessary to achieve a better understanding of this tumor. | |||||
書誌情報 |
BMC Research Notes 巻 8, p. 257, 発行日 2015-06-24 |
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出版者 | ||||||
出版者 | BioMed Central | |||||
EISSN | ||||||
収録物識別子タイプ | ISSN | |||||
収録物識別子 | 17560500 | |||||
DOI | ||||||
関連タイプ | isIdenticalTo | |||||
識別子タイプ | DOI | |||||
関連識別子 | 10.1186/s13104-015-1233-6 | |||||
権利 | ||||||
権利情報 | c 2015 Shida et al. | |||||
権利 | ||||||
権利情報 | This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. | |||||
著者版フラグ | ||||||
出版タイプ | VoR | |||||
出版タイプResource | http://purl.org/coar/version/c_970fb48d4fbd8a85 | |||||
引用 | ||||||
内容記述タイプ | Other | |||||
内容記述 | BMC Research Notes, 8, 257; 2015 |