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胸主动脉壁内血肿的诊断与治疗

Diagnosis and treatment of thoracic aortic intramural hematoma.

作者信息

Muluk S C, Kaufman J A, Torchiana D F, Gertler J P, Cambria R P

机构信息

Department of Surgery, Massachusetts General Hospital, Harvard Medical School, Boston, USA.

出版信息

J Vasc Surg. 1996 Dec;24(6):1022-9. doi: 10.1016/s0741-5214(96)70048-4.

Abstract

PURPOSE

This report reviews our recent experience with nine patients who had intramural hematoma of the thoracic aorta.

METHODS

This was a retrospective study of all patients who had intramural hematoma at our institution from 1989 to 1994. Patients who had identifiable intimal flap, tear, or penetrating aortic ulcer were excluded from the study.

RESULTS

Among these nine elderly patients (mean age, 76 years), the most common presentation was chest or back pain. Intramural hematoma was diagnosed by a variety of high-resolution imaging techniques. The descending thoracic aorta alone was involved in seven patients, whereas the ascending aorta was affected in the other two patients. One patient had evidence of an aneurysm (5.0 cm diameter) in the region of the hematoma. All patients were initially managed nonsurgically with blood pressure control. Both patients who had ascending aortic involvement had progression of aortic hematoma, which resulted in death in one case and in successful surgery in the other. Six of the seven patients who had descending aortic involvement alone were successfully managed without aortic surgery. The patient who had intramural hematoma and associated aortic aneurysm, however, had severe, recurrent pain and underwent successful aortic replacement. Another patient had recurrent pain associated with hypertension, but was successfully managed nonsurgically with antihypertensive therapy. All eight survivors are doing well at a median follow-up of 19 months.

CONCLUSIONS

Intramural hematoma appears to be a distinct entity, although overlap with aortic dissection or penetrating aortic ulcer exists. Aggressive control of blood pressure with intensive care unit monitoring has been our initial management. Patients who have involvement of the descending thoracic aorta alone can frequently be managed without surgery in the absence of coexisting aneurysmal dilatation or disease progression. Our experience suggests that a more aggressive approach with early surgery is warranted in patients who have ascending aortic involvement or those who have coexisting aneurysm and intramural hematoma.

摘要

目的

本报告回顾了我们近期对9例胸主动脉壁内血肿患者的治疗经验。

方法

这是一项对1989年至1994年在我院发生壁内血肿的所有患者进行的回顾性研究。有可识别内膜瓣、撕裂或穿透性主动脉溃疡的患者被排除在研究之外。

结果

在这9例老年患者(平均年龄76岁)中,最常见的表现是胸痛或背痛。壁内血肿通过多种高分辨率成像技术得以诊断。仅降胸主动脉受累的患者有7例,而升主动脉受累的患者有2例。1例患者在血肿区域有动脉瘤证据(直径5.0 cm)。所有患者最初均采用非手术治疗以控制血压。升主动脉受累的2例患者主动脉血肿均有进展,其中1例死亡,另1例手术成功。仅降主动脉受累的7例患者中有6例未经主动脉手术即成功治疗。然而,有壁内血肿并伴有主动脉瘤的患者有严重的复发性疼痛,接受了成功的主动脉置换术。另1例患者有与高血压相关的复发性疼痛,但通过抗高血压治疗非手术成功治疗。8例幸存者在中位随访19个月时情况良好。

结论

壁内血肿似乎是一种独特的疾病,尽管与主动脉夹层或穿透性主动脉溃疡存在重叠。在重症监护病房监测下积极控制血压一直是我们的初始治疗方法。仅降胸主动脉受累的患者,在不存在并存动脉瘤样扩张或疾病进展的情况下,通常无需手术即可治疗。我们的经验表明,对于升主动脉受累或并存动脉瘤和壁内血肿的患者,有必要采取更积极的早期手术方法。

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