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ID 35836
本文ファイル
著者
Adhikari, Rupendra B
Eguchi, Kuniki
キーワード
ADPKD
endovascular treatment
subarachnoid hemorrhage
unruptured aneurysm
NDC
医学
抄録(英)
Autosomal dominant polycystic kidney disease (ADPKD) is a common single gene hereditary disorder characterized by progressive development of bilateral renal cysts eventually leading to chronic kidney disease and an array of extrarenal abnormalities including intracranial aneurysm (ICAN). While the association of ICAN with ADPKD is undisputed, its management is not standardized. Conflicting data about the benefits of screening to the efficacy of different treatment modalities have not helped establish any opinion. We report three such cases managed surgically at Hiroshima University Hospital and discuss and review the literature regarding ADPKD and ICAN. Decision for surgical management of these cases were multifactorial and not exclusively because of ADPKD. There is a lack of sufficient randomized data on these topics and until such results are available, neurosurgeons are likely to resort to bit-part data and weigh the risk-benefit factor in individual patients and proceed accordingly.
掲載誌名
Nepal Journal of Neuroscience
10巻
2号
開始ページ
81
終了ページ
85
出版年月日
2013
出版者
Neuroscience Publishing Group
ISSN
1813-1948
言語
英語
NII資源タイプ
学術雑誌論文
広大資料タイプ
学術雑誌論文
DCMIタイプ
text
フォーマット
application/pdf
著者版フラグ
publisher
権利情報
(c) Neuroscience Publishing Group
部局名
医歯薬学総合研究科