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症例
粘液腫切除によりOrtner症候群が改善した1例
Ortner Syndrome Complicated with Giant Myxoma:Report of a Case
岡田 修一
1
,
江連 雅彦
1
,
森下 寛之
1
,
長谷川 豊
1
,
山田 靖之
1
,
星野 丈二
1
,
井戸田 佳史
1
,
関 雅浩
1
,
田村 重樹
1
,
早田 隆司
1
Shuichi Okada
1
,
Masahiko Ezure
1
,
Hiroyuki Morishita
1
,
Yutaka Hasegawa
1
,
Yasuyuki Yamada
1
,
Joji Hoshino
1
,
Yoshifumi Itoda
1
,
Masahiro Seki
1
,
Kazuki Tamura
1
,
Takashi Soda
1
1群馬県立心臓血管センター心臓血管外科
1Division of Cardiovascular Surgery, Gunma Prefectural Cardiovascular Center
キーワード:
巨大左房粘液腫
,
Ortner症候群
,
声帯麻痺
Keyword:
giant myxoma
,
Ortner syndrome
,
recurrent nerve paralysis
pp.1021-1025
発行日 2024年11月1日
Published Date 2024/11/1
DOI https://doi.org/10.15106/j_kyobu77_1021
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- 参考文献 Reference
はじめに 左房粘液腫は比較的まれな疾患であり,さまざまな症状を呈する.われわれは,急速増大したと考えられる巨大左房粘液腫によりOrtner症候群を合併した1例を経験したので報告する.
A 68-year-old woman were admitted with chief complaints of persistent hoarseness, dysphagia and dyspnea on effort. She was found to have a left atrial myxoma with obstruction of mitral inflow on echocardiogram. The tumor was extensively attached to the atrial septum and left atrium. She underwent successful excision of the myxoma using cardiopulmonary bypass support with an uneventful recovery. The histopathological findings confirmed recent hemorrhage into the myxoma. She was discharged without complications 21 days after the operation. Hoarseness was improved and swallowing function was restored.
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