巨细胞动脉炎的升主动脉瘤

C. Özbek, U. Yetkin, Kaz m Ergüne, M. Akyuz, smail Yürekli, N. Postac, A. Çall, M. Aksun, A. Gürbüz
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引用次数: 1

摘要

巨细胞动脉炎(GCA)是一种相对常见的全身性血管炎。GCA是一种涉及大中型血管的全身性血管炎,它增加了患胸主动脉瘤的风险,这是一种罕见的原因。我们报告一例巨细胞动脉炎合并升主动脉瘤。治疗医师在评估GCA患者是否有胸、腹主动脉瘤时应保持警惕,因为这可能是GCA的并发症。巨细胞动脉炎(Giant cell arteritis, GCA)是一种中、大血管炎,是60岁以上人群中最常见的系统性血管炎。临床特征五花八门,有时令人误解。急性期反应升高,如高红细胞沉降率和c反应蛋白水平升高,是诊断的重要线索,这可以通过颞动脉活检阳性来保证。其他血管表现包括中风、主动脉瘤或夹层,甚至主动脉破裂。我们的病例是一名59岁的女性。既往有10年高血压病史。此外,一年前,她曾被诊断为GCA,并经颞浅动脉活检证实。因此,从那时起,她一直在接受类固醇治疗。3年前因心悸检查时发现升主动脉动脉瘤性扩张(54毫米)。经胸超声心动图显示升主动脉瘤大小为55mm,有中度主动脉反流。行心导管术。升主动脉扩张检查(图1)。冠状动脉正常。我们咨询了风湿病科的术前和术后建议。图1患者在气管内全身麻醉下,仰卧位手术。胸骨正中切开术后,纵向打开心包。升主动脉扩张。由于在头臂干近端有合适的颈部,因此不需要腋窝和股动脉插管。肝素化后,腹腔静脉与升主动脉之间建立体外循环。在主动脉上放置一个十字夹,逆行连续等温血。在巨细胞性动脉炎中,5例从冠状窦引起的心脏骤停中有2例被确定为心脏骤停。体温过低为中度(28℃)。通过右上肺静脉放置通气管。行标准主动脉切开术。十字钳右近端有主动脉段,适合远端吻合。探查主动脉瓣。右冠状动脉尖自由缘心室面可见0.5x0.5 cm的钙化疣状结构(图2)。
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Ascending Aortic Aneurysm In Giant Cell Arteritis
Giant cell arteritis(GCA) is a relatively common form of systemic vasculitis. GCA is a systemic vasculitis which involves large and medium sized vessels,and it increases the risk of developing a thoracic aortic aneurysm and it is a rare cause.We describe a case of ascending aortic aneurysm in giant cell arteritis. The treating physician should be vigilant in assessing the patient with GCA for thoracic and abdominal aortic aneurysms that are feared complications of GCA. INTRODUCTION Giant cell arteritis(GCA) is a mediumand large-vessel vasculitis, the most prevalent systemic vasculitis in subjects over age 60. Clinical features are miscellaneous and sometimes misleading. Elevated acute-phase responses, such as a high erythrocyte sedimentation rate and increased levels of C-reactive protein, are important clues to the diagnosis, which is ensured by a positive temporal artery biopsy[1]. Additional vascular manifestations include stroke, aortic aneurysm or dissection, and even aortic rupture[2]. CASE PRESENTATION Our case was a 59-year-old female. Her past medical history was significant for hypertension for 10 years. Moreover, she had been diagnosed as having GCA confirmed with biopsy of superficial temporal artery a year ago. Therefore she had been under steroid therapy since then. She also had an aneurysmal dilation of the ascending aorta (54 mm) which was revealed 3 years ago during investigations for palpitation.In transthoracic echocardiogram ascending aortic aneurysm size was 55mm and she had moderate aortic regurgitation. Cardiac catheterization was performed. Ascending aortic dilation was investigated(Figure 1). Coronary arteries were normal. Department of Rheumatology was consulted for preand postoperative recommendations. Figure 1 Figure 1 She was operated under endotracheal general anesthesia and in supine position.Following a median sternotomy,pericardium was opened longitudinally. Ascending aorta was dilated. Since there was a suitable neck just proximal to brachiocephalic trunk, neither axillary nor femoral cannulation was needed. After heparinization, extracorporeal circulation was established between the venae cavae and the ascending aorta. A cross clamp was placed on aorta and by retrograde continuous isothermic blood Ascending Aortic Aneurysm In Giant Cell Arteritis 2 of 5 cardioplegia from coronary sinus,cardiac arrest was established.Hypothermia was moderate (28oc).A vent was placed via the right superior pulmonary vein.Standard aortotomy was made. There was an aortic segment right proximal to the crossclamp, suitable for distal anastomosis. Aortic valve was explored. There was a calcified verrucous structure of 0.5x0.5 cm on the ventricular aspect of the free edge of the right coronary cusp (Figure 2).
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