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与川崎病相关的巨大冠状动脉瘤,30年间呈现进行性扩张。

Giant coronary artery aneurysm associated with Kawasaki disease showing progressive dilation over 30 years.

作者信息

Fujioka Tao, Asakawa Nanae, Suzuki Toshihiko, Kobayashi Jotaro, Takahashi Kei, Tsuchiya Keiji

机构信息

Department of Pediatrics, Japanese Red Cross Medical Center, 4-1-22 Hiroo, Shibuya-ku, Tokyo 150-8935, Japan.

Department of Pathology, Toho University Ohashi Medical Center, Japan.

出版信息

J Cardiol Cases. 2021 Feb 11;23(6):281-284. doi: 10.1016/j.jccase.2021.01.011. eCollection 2021 Jun.

Abstract

A 33-year-old pregnant woman with a history of a giant coronary artery aneurysm (CAA) of the right coronary artery owing to Kawasaki disease (KD) was referred to our hospital for the management of pregnancy and delivery. The CAA was detected when she was 10 months old on the 24th day from the onset of KD and showed transient regression followed by progressive dilation and reached a size of 25 mm when she was 30 years old. The baby was delivered at 38 weeks of gestational age. Resection of the CAA and coronary artery bypass grafting were performed 5 months after the delivery. Pathological results suggest that progressive dilation of the CAA was owing to a reduction in elastic recoiling force caused by partial destruction of the internal elastic lamina and degenerated tunica media against an increase in blood pressure that accompanied the growth of the patient. The pathophysiology of CAAs with atypical clinical course may be different from that of typical CAAs owing to KD. < Kawasaki disease (KD) causes varying sizes of coronary artery aneurysms (CAAs). In this case, rare progressive dilation of the CAA owing to KD was observed in the remote phase. We revealed different pathological features of rare CAAs from those of a typical one; progressive dilation of the CAA could be owing to the reduction of recoiling force. Planned surgical treatment of a CAA showing continuous dilation should be a reasonable option for avoiding emergent CAA rupture.>.

摘要

一名33岁的孕妇因川崎病(KD)导致右冠状动脉巨大冠状动脉瘤(CAA),被转诊至我院进行妊娠和分娩管理。该CAA在她10个月大时,即KD发病后第24天被发现,起初有短暂缩小,随后逐渐扩张,在她30岁时直径达到25毫米。婴儿在孕38周时出生。产后5个月进行了CAA切除和冠状动脉搭桥术。病理结果表明,CAA的逐渐扩张是由于随着患者生长血压升高,内部弹性膜部分破坏和中膜退变导致弹性回缩力降低所致。非典型临床病程的CAA的病理生理学可能与KD所致典型CAA不同。<川崎病(KD)可导致不同大小的冠状动脉瘤(CAA)。在本病例中,在疾病后期观察到了罕见的因KD导致的CAA进行性扩张。我们发现罕见CAA与典型CAA具有不同的病理特征;CAA的进行性扩张可能是由于回缩力降低。对于持续扩张的CAA,计划进行手术治疗应是避免CAA紧急破裂的合理选择。>

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