Yamada Shunsuke, Kohno Tadasu
Department of Thoracic Surgery, Toranomon Hospital, Tokyo, Japan.
Ann Thorac Surg. 2004 Jun;77(6):1911-5. doi: 10.1016/j.athoracsur.2003.12.040.
Small, well-circumscribed pure ground-glass opacities on high-resolution computed tomography can represent either localized bronchioloalveolar carcinoma without foci of active fibroblastic proliferation, or atypical adenomatous hyperplasia. Since neither lesion displays lymph node metastasis, excellent prognosis can be expected even with limited surgical resection. In this study, video-assisted thoracic surgery was performed for patients with pure ground-glass-opacity to evaluate efficacy for both diagnostic and therapeutic purposes.
Thirty-nine patients with pure ground-glass opacity less than or equal to 2 cm in diameter (62 lesions) underwent video-assisted thoracic surgery with wedge resection as primary therapy. Histologic diagnoses were made according to Noguchi classifications.
Single lesions were observed in 30 patients, with multiple lesions (mean, 4 lesions) in 9 patients. Twenty-eight patients underwent wedge resection. Seven patients underwent lobectomy or segmentectomy for technical reasons. Four patients underwent conversion of wedge resection to lobectomy (due to active fibroblastic proliferation in 2 patients, and other reasons in 2 patients). All procedures were performed under videoscopic observation. Histologic diagnoses comprised localized bronchioloalveolar carcinoma without active fibroblastic proliferation either alone or in combination with atypical adenomatous hyperplasia in 29 patients, atypical adenomatous hyperplasia in 8 patients, and localized bronchioloalveolar carcinoma with active fibroblastic proliferation in 2 patients. All patients with localized bronchioloalveolar carcinoma underwent follow-up for a median period of 29.3 months, and have survived without sign of recurrence.
Video-assisted thoracic surgery may be appropriate for management of small pure ground-glass opacities.
高分辨率计算机断层扫描上小的、边界清晰的纯磨玻璃样混浊可代表无活跃纤维母细胞增殖灶的局限性细支气管肺泡癌,或非典型腺瘤样增生。由于这两种病变均不显示淋巴结转移,即使进行有限的手术切除,预后也有望良好。在本研究中,对纯磨玻璃样混浊的患者进行了电视辅助胸腔镜手术,以评估其诊断和治疗效果。
39例直径小于或等于2 cm的纯磨玻璃样混浊患者(62个病灶)接受了电视辅助胸腔镜手术,以楔形切除作为主要治疗方法。根据野口分类法进行组织学诊断。
30例患者观察到单个病灶,9例患者有多个病灶(平均4个病灶)。28例患者接受了楔形切除。7例患者因技术原因接受了肺叶切除术或肺段切除术。4例患者由楔形切除转为肺叶切除术(2例因活跃的纤维母细胞增殖,2例因其他原因)。所有手术均在电视镜观察下进行。组织学诊断包括29例无活跃纤维母细胞增殖的局限性细支气管肺泡癌,单独或合并非典型腺瘤样增生,8例非典型腺瘤样增生,2例有活跃纤维母细胞增殖的局限性细支气管肺泡癌。所有局限性细支气管肺泡癌患者的中位随访时间为29.3个月,均存活且无复发迹象。
电视辅助胸腔镜手术可能适用于小的纯磨玻璃样混浊的治疗。