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タイトル: Paraurachal paraganglioma
著者: Tsuruta, Masafumi
Goto, Takayuki
Kono, Jin
Kita, Yuki
Masui, Kimihiko  kyouindb  KAKEN_id
Sano, Takeshi
Fujimoto, Masakazu  kyouindb  KAKEN_id  orcid https://orcid.org/0000-0002-0575-6507 (unconfirmed)
Sawada, Atsuro
Akamatsu, Shusuke
Kobayashi, Takashi
著者名の別形: 後藤, 崇之
河野, 仁
北, 悠希
増井, 仁彦
佐野, 剛視
藤本, 正数
澤田, 篤郎
赤松, 秀輔
小林, 恭
キーワード: chromaffin cells
paraganglioma
urachus
発行日: Sep-2022
出版者: Wiley
誌名: IJU Case Reports
巻: 5
号: 5
開始ページ: 358
終了ページ: 361
抄録: Introduction: Paragangliomas (PGLs) are frequently reported around the abdominal aorta; however, are extremely rare near the urachus.
Case presentation: A 78-year-old woman was referred to the urology department of our hospital for further examination and treatment of a 1.2-cm tumor in the lower abdominal wall, a tumor excision was then performed. On immunohistochemical staining, the tumor and supporting cells were positive for chromogranin A and the S 100 protein, respectively, and were diagnosed as PGL. The PGL was thought to be derived from chromaffin cells that migrated to the wall of the urachus during embryonic life and remained even after the wall regressed.
Conclusion: We report a case of PGL near the urachus that can be explained by the distribution of the sympathetic network around the midline of the lower abdominal wall during embryonic development. Therefore, PGL should be considered in the differential diagnosis of periurachal tumors.
著作権等: © 2022 The Authors. IJU Case Reports published by John Wiley & Sons Australia, Ltd on behalf of Japanese Urological Association.
This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
URI: http://hdl.handle.net/2433/293668
DOI(出版社版): 10.1002/iju5.12488
PubMed ID: 36090947
出現コレクション:学術雑誌掲載論文等

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