Tanaka Yusuke, Matsumoto Isao, Saito Daisuke, Yoshida Syuhei, Kakegawa Seiichi, Tamura Masaya, Takemura Hirofumi, Yoshimura Kaori, Ikeda Hiroko
Department of General, Thoracic and Cardiovascular Surgery, Kanazawa University, Kanazawa, Japan.
Kyobu Geka. 2017 Mar;70(3):169-173.
We reported a case of bronchial atresia requiring differentiation from the intralobar sequestration. A 42-year-old man was referred to our institution with suspicion of intralobar sequestration, based on a 3-dimensional computed tomography (CT) angiography that showed abnormal blood vessels from the right inferior phrenic artery flowing into the right lower lobe. CT revealed a lesion between S9 and S10 wherein there were refluxed blood vessels from A9 without an accompanying bronchus, with polycysts and emphysematous changes. Ventilation-perfusion scintigraphy revealed a reduction in uptake in the same sites. He was diagnosed as congenital bronchial atresia preoperatively, and we performed a right basal segmentectomy. Pathological examination confirmed the bronchiectasis and emphysematous changes in the lung parenchyma, but malignant findings were not confirmed.
我们报告了一例需要与肺叶内隔离症相鉴别的支气管闭锁病例。一名42岁男性因怀疑肺叶内隔离症被转诊至我院,其三维计算机断层扫描(CT)血管造影显示有异常血管从右下膈动脉流入右下叶。CT显示在S9和S10之间有一个病变,其中有来自A9的反流血管,但无伴行支气管,伴有多囊和肺气肿改变。通气-灌注闪烁扫描显示相同部位摄取减少。术前诊断为先天性支气管闭锁,我们实施了右肺基底段切除术。病理检查证实肺实质有支气管扩张和肺气肿改变,但未发现恶性病变。