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タイトル: Successful flow reduction surgery for a ruptured true posterior communicating artery aneurysm caused by the common carotid artery ligation for epistaxis.
著者: Yamao, Yukihiro  KAKEN_id  orcid https://orcid.org/0000-0002-9615-2353 (unconfirmed)
Takahashi, Jun C
Satow, Tetsu
Iihara, Koji
Miyamoto, Susumu
著者名の別形: 山尾, 幸広
宮本, 享
キーワード: Common carotid artery ligation
extra-intracranial bypass
flow reduction
true posterior communicating artery aneurysm
発行日: 28-Nov-2014
出版者: Medknow Publications
誌名: Surgical neurology international
巻: 5
開始ページ: S501
終了ページ: S505
抄録: [Background]: Carotid artery occlusion can lead to the development of rare true posterior communicating artery (PCoA) aneurysms because of hemodynamic stress on the PCoA. Surgical treatment of these lesions is challenging. [Case Description]: The authors report a case of a true PCoA aneurysm that developed and ruptured 37 years after ligation of the ipsilateral common carotid artery for epistaxis. The lesion was successfully treated with clipping of the distal M1 segment of the middle cerebral artery (MCA) after the occipital artery-radial artery free graft-MCA bypass, which led to extreme reduction in collateral flow through the PCoA. A cortical branch, located just proximal to the obliteration site, functioned as a sufficient flow outlet. The aneurysm shrank, and the patient has been doing well without any symptoms for 5 years after surgery. [Conclusions]: M1 obliteration combined with high-flow extra-intracranial bypass might be a promising option for a true PCoA aneurysm, and therapeutic design that leaves a sufficient flow outlet on the M1 is mandatory to avoid unexpected occlusion of the M1 and its perforators.
著作権等: © 2014 Yamao et al; This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
URI: http://hdl.handle.net/2433/193268
DOI(出版社版): 10.4103/2152-7806.145657
PubMed ID: 25525556
出現コレクション:学術雑誌掲載論文等

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