annulo aortic ectasia

大動脈弁輪拡張症 AAE

WordNet

1. dilatation or distension of a hollow organ (同)ectasis

PrepTutorEJDIC

1. 〈法律など〉'を'無効にする;〈命令など〉'を'取り消す(cancel)

UpToDate Contents

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• 1. 大動脈解離の臨床症状および診断 clinical manifestations and diagnosis of aortic dissection
• 2. マルファン症候群および関連疾患の遺伝学、臨床的特徴、および診断 genetics clinical features and diagnosis of marfan syndrome and related disorders
• 3. 成人における大動脈二尖弁の臨床症状および診断 clinical manifestations and diagnosis of bicuspid aortic valve in adults
• 4. 胸部大動脈瘤の臨床症状および診断 clinical manifestations and diagnosis of thoracic aortic aneurysm
• 5. 成人における大動脈二尖弁疾患のマネージメント management of adults with bicuspid aortic valve disease

English Journal

• Long-term follow-up after implantation of the Shelhigh® No-React® complete biological aortic valved conduit†.

• Reineke DC1, Kaya A2, Heinisch PP3, Oezdemir B3, Winkler B3, Huber C3, Heijmen RH2, Morshuis W2, Carrel TP3, Englberger L3.
• European journal of cardio-thoracic surgery : official journal of the European Association for Cardio-thoracic Surgery.Eur J Cardiothorac Surg.2015 Dec 30. pii: ezv452. [Epub ahead of print]
• OBJECTIVES: Long-term follow-up reports after implantation of the Shelhigh® (Shelhigh, Inc., NJ, USA) No-React® aortic valved conduit used for aortic root replacement do not exist.METHODS: Between November 1998 and December 2007, the Shelhigh® No-React® aortic valved conduit was implanted in 291
• PMID 26719402

• [Familial Annulo-aortic Ectasia without Marfan Syndrome].

• Terada H1, Nakagawa H, Miyazaki T, Hiranuma S, Muto Y, Okuyama H, Nabuchi A, Endo M, Matsumoto Y, Izumi M.
• Kyobu geka. The Japanese journal of thoracic surgery.Kyobu Geka.2015 Dec;68(13):1049-52.
• Marfan syndrome is a hereditary disease that presents ocular, skeletal, and cardiovascular abnormalities. In recent years, there have been several reports of patients with familial cardiovascular disease but no physical features of Marfan syndrome. We encountered 3 cases of familial annulo-aortic ec
• PMID 26759943

• Bilateral internal thoracic artery grafting during David procedure complicated with coronary insufficiency.

• Ohira S1, Doi K1, Yaku H1.
• Nagoya journal of medical science.Nagoya J Med Sci.2015 Aug;77(3):521-4.
• A 47-year-old woman diagnosed with Marfan syndrome underwent valve-sparing aortic root replacement for aortic regurgitation and annulo-aortic ectasia. Her cardiac function was normal. Preoperative coronary angiography did not demonstrate any stenosis. The David reimplantation procedure with a 28-mm
• PMID 26412900

Japanese Journal

• 大動脈基部拡張症に対する外科治療 : 大動脈基部および大動脈弁の特徴と長期経過からみた手術術式の妥当性 (特集 進化した大動脈基部置換術)

• 胸部外科 = The Japanese journal of thoracic surgery 71(1), 4-9, 2018-01
• NAID 40021434643

• Bentall 原法術後遠隔期に冠動脈口吻合部仮性動脈瘤を繰り返した1例

• 日本心臓血管外科学会雑誌 45(5), 229-232, 2016
• NAID 130005249773

• 家族性に大動脈弁輪拡張症を有する非Marfan症候群の3姉弟

• 胸部外科 = The Japanese journal of thoracic surgery 68(13), 1049-1052, 2015-12
• NAID 40020659235

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★リンクテーブル★

関連記事	「ectasia」「aortic」

「ectasia」

　　[★]

拡張症

関

pathologic dilatation、pathological dilatation

　

「aortic」

　　[★]

• adj.

• 大動脈の

関

aorta、aortae、aortal