Department of Thoracic Surgery, Kanazawa Medical University, 1-1 Daigaku, Uchinada-machi, Kahoku-gun, Ishikawa, 920-0293, Japan.
Department of Palliative Care, Miyuki Hospital, Kumamoto, Japan.
J Cardiothorac Surg. 2022 Mar 23;17(1):52. doi: 10.1186/s13019-022-01791-0.
Anomalous systemic arterial supply to normal basal lung segments is a rare congenital malformation, in which aberrant arteries arising from the systemic circulation flow into the basal segment of the lung and return to normal pulmonary veins without abnormal bronchial branching. It presents a left-to-right shunt, resulting in volume overload of the pulmonary circulation, and consequently, pulmonary hypertension. Therefore, nearly all cases require surgery. Herein, we present a case, in which indocyanine green was used to demarcate the lung segment perfused by an anomalous systemic artery.
A 15-year-old boy was diagnosed with an anomalous artery originating from the celiac artery and supplying the right dorsobasal lung segment (S). Via three-port video-assisted thoracoscopic surgery, the anomalous artery was ligated and processed with an auto-stapler. Indocyanine green was injected intravenously to identify the tissue perfused by the anomalous artery, and the lung was resected.
With anomalous systemic arterial supply to normal basal lung segments, indocyanine green can be particularly helpful in identifying the boundaries of the perfused area. Then, the affected tissue can be resected by thoracoscopic surgery.
体循环异常动脉供应正常肺基底段是一种罕见的先天性畸形,其中源自体循环的异常动脉流入肺基底段,然后通过正常肺静脉回流,而无异常支气管分支。它会导致左向右分流,使肺循环血量过载,进而导致肺动脉高压。因此,几乎所有病例都需要手术治疗。本文报告了一例应用吲哚菁绿(ICG)标记体循环异常动脉供应的肺段的病例。
一名 15 岁男孩被诊断为起源于腹腔动脉的异常动脉供应右背侧基底段(S)。通过三孔电视辅助胸腔镜手术,结扎了异常动脉并用吻合器处理。静脉注射吲哚菁绿(ICG)以识别异常动脉供应的组织,然后切除肺部。
对于体循环异常动脉供应正常肺基底段,吲哚菁绿(ICG)可特别有助于识别灌注区域的边界。然后,通过胸腔镜手术切除受累组织。