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成人肺隔离症 1 例报告。

Intralobar pulmonary sequestration in an adult: a case report.

机构信息

Department of Cardiothoracic Surgery, The Alfred, 55 Commercial Road, Prahran, Melbourne, VIC, 3004, Australia.

出版信息

J Cardiothorac Surg. 2023 Jan 6;18(1):5. doi: 10.1186/s13019-023-02127-2.

Abstract

BACKGROUND

Pulmonary sequestration is a rare congenital lung anomaly, presenting mostly in childhood and adolescence.

CASE PRESENTATION

We report the case of a 26-year-old male patient presenting with pleuritic left sided chest pain and haemoptysis. Computed tomography of the chest showed features of intralobar pulmonary sequestration involving the left lower lobe, with arterial supply arising from the descending thoracic aorta above the diaphragm and normal venous drainage. Video assisted thoracic surgery was planned to perform a left lower lobectomy. Considering the risk of bleeding from the large artery supplying the sequestered segment, a posterolateral thoracotomy incision was made and left lower lobectomy was completed, with successful division of the arterial feeder. The patient was discharged home without complications. Pathologic examination of the specimen grossly revealed partial division of the lobe by two fissures with extensive adhesions into an upper and lower portion with no clear demarcation and a large vessel which enters the lower portion at the posterior inferior aspect, separate from the hilum with a diameter 10 mm. Microscopically, both portions of the lobe showed normally alveolated lung tissue with patchy recent intra-alveolar haemorrhage and evidence of chronic inflammation in the sequestered segment. There was no evidence of malignancy.

CONCLUSION

This case highlights the rare presentation of pulmonary sequestration in adulthood and the importance of imaging to identify anomalous arterial supply to the sequestered segment in the left lower lobe of the lung. The use of safe surgical techniques to control the anomalous systemic arterial feeding vessel cannot be overemphasized.

摘要

背景

肺隔离症是一种罕见的先天性肺畸形,主要发生在儿童和青少年时期。

病例报告

我们报告了一例 26 岁男性患者,表现为左侧胸痛和咯血。胸部计算机断层扫描显示左肺下叶肺隔离症的特征,动脉供应来自膈肌上方降主动脉,静脉回流正常。计划行电视辅助胸腔镜手术行左肺下叶切除术。考虑到供应隔离段的大动脉出血风险,行后外侧开胸切口,完成左肺下叶切除术,并成功分离动脉供应。患者无并发症出院。标本大体检查显示,两个裂将肺叶部分分隔,上下两部分广泛粘连,无明显界限,一条 10 毫米直径的大血管从后下方进入下部,与肺门分开。镜下,肺叶的两部分均显示正常肺泡化的肺组织,伴有斑片状近期肺泡内出血,以及隔离段慢性炎症的证据。没有恶性肿瘤的证据。

结论

本病例强调了肺隔离症在成年期的罕见表现,以及影像学对识别左肺下叶隔离段异常动脉供应的重要性。强调使用安全的手术技术控制异常的体循环动脉供血血管非常重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/072e/9824908/dc186a14ce62/13019_2023_2127_Fig1_HTML.jpg

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