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胸腔镜下使用三维模型和吲哚菁绿行肺隔离症肺段切除术

Thoracoscopic non-anatomical lung segmentectomy for intralobar pulmonary sequestration using a 3-dimensional model and indocyanine green.

机构信息

Thoracic Surgery Department, Curie-Montsouris Thorax Institute, Institut Mutualiste Montsouris, Paris, France School of Thoracic Surgery, University of Milan, Milan, Italy.

Thoracic Surgery Department, Curie-Montsouris Thorax Institute, Institut Mutualiste Montsouris, Paris, France.

出版信息

Multimed Man Cardiothorac Surg. 2024 Oct 30;2024. doi: 10.1510/mmcts.2024.101.

Abstract

Pulmonary sequestrations comprise a spectrum of congenital lung malformations, with abnormal lung tissue lacking connection with the tracheobronchial tree, supplied by an aberrant systemic artery. Until a few years ago, lobectomy was considered the standard treatment for intralobar pulmonary sequestration. However, minimally invasive sublobar resection gained a place as an interesting alternative therapeutic approach, guided by indocyanine green and computed tomography-based 3-dimensional anatomical models. Like pulmonary sequestrations,  pulmonary pseudosequestrations are a congenital lung malformation, but characterized by a normal lung tissue fed by systemic arterial branches. To the best of our knowledge, there are no published cases of pulmonary pseudosequestration combined with sequestration. We present a case of an intralobar pulmonary sequestration coupled with an adjacent pseudosequestration, resected using thoracoscopic surgery with the aid of a 3-dimensional anatomical model and indocyanine green.

摘要

肺隔离症是一种先天性肺畸形,其特征为异常肺组织与气管支气管树无连接,由异常体循环动脉供血。直到几年前,肺叶切除术一直被认为是治疗肺隔离症的标准方法。然而,在吲哚菁绿和基于 CT 的三维解剖模型的引导下,微创亚肺叶切除术作为一种有趣的治疗方法获得了一席之地。与肺隔离症一样,假性肺隔离症也是一种先天性肺畸形,但由体循环动脉分支供应正常肺组织。据我们所知,目前尚无合并假性肺隔离症的肺隔离症的报道。我们报告了一例肺隔离症合并邻近假性肺隔离症的病例,该病例采用三维解剖模型和吲哚菁绿辅助的电视胸腔镜手术切除。

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