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1例患有内脏逆位综合征的患者因原发性肺癌接受右肺中叶切除术。

A case of right middle lobectomy for primary lung cancer in a patient with heterotaxy syndrome.

作者信息

Demura Ryo, Imai Kazuhiro, Takashima Shinogu, Kurihara Nobuyasu, Kuriyama Shoji, Suzuki Haruka, Harata Yuzu, Minamiya Yoshihiro

机构信息

Department of Thoracic Surgery, Akita University Graduate School of Medicine, 1-1-1 Hondo, Akita, 010-8543, Japan.

出版信息

Gen Thorac Cardiovasc Surg Cases. 2024 Nov 22;3(1):52. doi: 10.1186/s44215-024-00177-z.

Abstract

BACKGROUND

Anatomical abnormalities in the pulmonary vessels have long aroused great interest among thoracic surgeons, and numerous variations of pulmonary vessels have been reported. Heterotaxy syndrome is an anatomical abnormality in which typically asymmetrical organs, including the lungs, develop symmetrically. We report the case of a 71-year-old man with heterotaxy syndrome undergoing radical lobectomy in the treatment of non-small cell lung cancer.

CASE PRESENTATION

Computed tomography (CT) revealed an irregular nodule 25 mm in diameter in the right middle lobe. Two months later, at his first visit to our University Hospital, CT revealed a rapidly growing tumor 60 mm in diameter. In addition, three-dimensional (3D) CT revealed the upper and middle lobar bronchi forming a common trunk with the mediastinal type of the right pulmonary artery (PA). The patient underwent video-assisted right middle lobectomy + systematic complete hilar and mediastinal lymph node dissection. The interlobar fissure between the right upper and middle lobes was incomplete, and the common trunk formed by the upper-middle bronchus emerged from an area between the right PA (A) and the right superior pulmonary vein.

CONCLUSION

The finding of A branching from the right main PA and descending posterior to the right upper-middle bronchus, which formed a common trunk, resembled a mirror image of the normal left lung. To our knowledge, a common trunk with the mediastinal type of the right PA has never been reported during video-assisted right middle lobectomy. In patients with heterotaxy syndrome, 3D-CT to preoperatively understand their anatomy is essential.

摘要

背景

肺血管的解剖异常长期以来一直引起胸外科医生的极大兴趣,并且已经报道了许多肺血管变异情况。内脏反位综合征是一种解剖异常,其中包括肺在内的典型不对称器官呈对称发育。我们报告了一例71岁患有内脏反位综合征的男性患者,接受根治性肺叶切除术治疗非小细胞肺癌。

病例介绍

计算机断层扫描(CT)显示右中叶有一个直径25毫米的不规则结节。两个月后,患者首次就诊于我院时,CT显示肿瘤迅速生长至直径60毫米。此外,三维(3D)CT显示上叶和中叶支气管与纵隔型右肺动脉(PA)形成一个共同主干。患者接受了电视辅助右中叶切除术+系统性完全肺门和纵隔淋巴结清扫术。右上叶和中叶之间的叶间裂不完整,由上中叶支气管形成的共同主干从右肺动脉(A)和右上肺静脉之间的区域发出。

结论

右主肺动脉分支并在右上中叶支气管后方下行形成共同主干的情况,类似于正常左肺的镜像。据我们所知,在电视辅助右中叶切除术中,从未报道过纵隔型右肺动脉形成共同主干的情况。对于患有内脏反位综合征的患者,术前通过3D-CT了解其解剖结构至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b9b6/11583655/15d225566b16/44215_2024_177_Fig1_HTML.jpg

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