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[与特纳综合征相关的主动脉夹层]

[Aortic dissection associated with Turner's syndrome].

作者信息

Ota Y, Tsunemoto M, Shimada M, Ishizawa A, Koike K, Kobayashi J

机构信息

Department of Cardiovascular Surgery & Cardiology, National Children's Hospital.

出版信息

Kyobu Geka. 1992 May;45(5):411-4.

PMID:1593810
Abstract

We report two cases of Turner's syndrome who had had coarctation repair and who ultimately died from complications believed to be associated with Turner's stigmata. Case 1. The repair of coarctation of the aorta (Co/Ao) at age 5 was associated with the tear of the aortic wall and an Asc. Ao-Desc. Ao bypass together with the closure of the Ao proximal to the Co/Ao was performed. At age 10, she developed a dissecting aneurysm of the Asc. Ao seemingly unrelated to the previous surgery and the Asc. Ao was replaced by a prosthetic tube graft. Pathological diagnosis was cystic medionecrosis. The aortic valve was bicuspid. Subsequently, the patient showed progressive worsening of the aortic regurgitation. The aortic valve replacement at age 14 was complicated by significant bleeding and the patient died on the fifth postoperative day. Case 2. Co/Ao was repaired at age 8. During the operation, the aortic wall appeared to be thin and friable, and there was some tear of the posterior suture line which necessitated reanastomosis with resultant stenosis. At age 9, stenotic area was enlarged by an onlay-patch of a piece of woven Dacron arterial graft. There was gradual swelling of that area on routine x-ray examinations and an aortography at age 16 showed definite aneurysm formation. At age 18, she suddenly developed hemoptysis. Rupture of the aneurysm into the pleural cavity and the left lung was suspected. An emergency surgery to stop bleeding under hypothermic cardiopulmonary bypass was unsuccessful and the patient died in OR.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

我们报告了两例患有特纳综合征且接受过主动脉缩窄修复术的病例,最终均死于被认为与特纳综合征体征相关的并发症。病例1。患者5岁时进行主动脉缩窄(Co/Ao)修复术,术中出现主动脉壁撕裂,遂行升主动脉-降主动脉旁路移植术并封闭主动脉缩窄近端。10岁时,她发生升主动脉夹层动脉瘤,似乎与之前的手术无关,于是进行了人工血管置换。病理诊断为囊性中层坏死。主动脉瓣为二叶式。随后,患者主动脉反流逐渐加重。14岁时进行主动脉瓣置换术,术后出现严重出血,患者于术后第5天死亡。病例2。患者8岁时进行主动脉缩窄修复术。术中发现主动脉壁薄且脆,后缝合线有撕裂,需重新吻合,结果导致狭窄。9岁时,用一块编织涤纶动脉补片扩大狭窄区域。常规X线检查发现该区域逐渐肿胀,16岁时主动脉造影显示有明确的动脉瘤形成。18岁时,她突然咯血。怀疑动脉瘤破裂进入胸腔和左肺。在低温体外循环下进行的紧急止血手术失败,患者在手术室死亡。(摘要截选至250字)

相似文献

1
[Aortic dissection associated with Turner's syndrome].[与特纳综合征相关的主动脉夹层]
Kyobu Geka. 1992 May;45(5):411-4.
2
Acute aortic dissection, aortic insufficiency, and a single coronary artery in a patient with Turner's syndrome.
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3
Dissection of the aorta in Turner's syndrome.特纳综合征患者的主动脉夹层分离
J Med Genet. 1983 Feb;20(1):61-3. doi: 10.1136/jmg.20.1.61.
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Aortic dissection and Turner's syndrome: case report and review of the literature.主动脉夹层与特纳综合征:病例报告及文献综述
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J Cardiovasc Surg (Torino). 1997 Jun;38(3):257-9.
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Ruptured aortic dissecting aneurysm in Turner's syndrome: a case report and review of literature.特纳综合征中的主动脉夹层动脉瘤破裂:一例报告并文献复习
Ann Thorac Cardiovasc Surg. 2000 Aug;6(4):275-80.
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Balloon angioplasty before Wheat's operation in a patient with Turner's syndrome.一名患有特纳综合征的患者在进行惠特手术前接受球囊血管成形术。
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[Chronic dissecting aortic aneurysm and Turner's syndrome. Apropos of a case].[慢性主动脉夹层动脉瘤与特纳综合征。附病例报告]
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Turner's syndrome and cardiovascular anomalies: a case report and review of the literature.特纳综合征与心血管异常:一例病例报告及文献综述
Am J Med Sci. 1989 Apr;297(4):260-2. doi: 10.1097/00000441-198904000-00014.

引用本文的文献

1
Dissection of the aorta in Turner syndrome: two cases and review of 85 cases in the literature.特纳综合征患者的主动脉夹层:两例病例及文献中85例病例的回顾
BMJ Case Rep. 2009;2009:bcr0620091998. doi: 10.1136/bcr.06.2009.1998. Epub 2009 Jul 1.
2
Dissection of the aorta in Turner syndrome: two cases and review of 85 cases in the literature.特纳综合征主动脉夹层:两例报告并文献中85例病例回顾
J Med Genet. 2007 Dec;44(12):745-9. doi: 10.1136/jmg.2007.052019. Epub 2007 Sep 14.
3
Aortic dissecting aneurysm with a bicuspid aortic valve in Turner's syndrome: report of a case.
Surg Today. 2007;37(8):667-70. doi: 10.1007/s00595-006-3462-8. Epub 2007 Jul 26.