Okamoto Koji, Ochiai Yoshie, Joo Kunihiko, Yamashita Yoshiyuki, Nakata Yusuke, Muneuchi Jun, Tokunaga Shigehiko
Department of Cardiovascular Surgery, Japan Community Healthcare Organization (JCHO) Kyushu Hospital, Kitakyushu-city, Japan.
Department of Pediatric Cardiology, Japan Community Healthcare Organization (JCHO) Kyushu Hospital, Kitakyushu-city, Japan.
Ann Thorac Surg Short Rep. 2023 Feb 20;1(2):325-327. doi: 10.1016/j.atssr.2023.02.004. eCollection 2023 Jun.
Herein, we describe a 21-month-old girl with PHACE syndrome (posterior fossa hemangiomas, arterial lesions, cardiac anomalies/coarctation of the aorta, and eye anomalies) who presented with a tortuous extensive aortic arch aneurysm. As the maximum short diameter of the distal aortic arch aneurysm expanded rapidly from 21 mm to 25 mm in only 5 months, we performed extensive aortic arch reconstruction with interposition graft replacement through a left thoracotomy under partial cardiopulmonary bypass.
在此,我们描述了一名患有PHACE综合征(后颅窝血管瘤、动脉病变、心脏异常/主动脉缩窄以及眼部异常)的21个月大女童,她出现了一个迂曲的广泛性主动脉弓动脉瘤。由于仅在5个月内,远端主动脉弓动脉瘤的最大短径就从21毫米迅速扩大到25毫米,我们在部分体外循环下通过左胸切口进行了带血管移植的广泛性主动脉弓重建术。