Features of preparation and surgical aspects of treatment of patients with ACTH-producing neuroendocrine lung tumors

M. Y. Pikunov, A. A. Pechetov, O. Golounina, S. Buryakina, L. Y. Rozhinskaya, Z. Belaya
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引用次数: 2

Abstract

BACKGROUND: The Department of Thoracic Surgery of the National Medical Research Center of Surgery named after A. V. Vishnevsky has been dealing with the problem of surgical treatment of patients with neuroendocrine lung tumors for more than 20 years. This article presents the experience of treating patients with ectopic ACTH syndrome over the past 15 years.AIM: To study the features of preparation, surgical aspects of treatment and delayed results in patients with ACTH-producing tumors of bronchopulmonary localization.MATERIALS AND METHODS: The study included 55 patients who underwent surgical treatment of ACTH-producing neuroendocrine tumor of bronchopulmonary localization in the period from 2005 to 2020. In order to systematize the approach to surgical treatment and the choice of the type of operation, a point analysis of the patient’s severity has been developed. Demographic information about patients, anamnesis data, results of hormonal and instrumental studies at pre- and postoperative stages and long-term treatment results were analyzed. The control period of observation of patients after surgery ranged from 6 months to 5 years.RESULTS: The age of the patients ranged from 18 to 72 years (36±15). According to the MSCT results of the chest, neoplasms in the lungs ranging in size from 5 to 25 mm were detected. Patients who scored from 18 to 23 points had lung resection due to the severity of the condition. With a total score from 14 to 18, segmentectomy with lymph node dissection was performed. When the total score was less than 14, a lobectomy with lymph node dissection was performed. During the planned histological examination, lung neuroendocrine tumor of various differentiation degree was confirmed in all patients. The results of treatment were followed in the period from 6 to 60 months, with a median of 19 months [10;24]. Regression of clinical manifestations of hypercortisolism after 1 year of dynamic follow-up period was detected in 83% of patients. After 60 months of follow-up 10 patients (71.4%) had a persistent clinical effect after surgical treatment with complete regression of hypercortisolism symptoms.CONCLUSION: The analysis of the results of surgical treatment, according to the proposed methodological aspects, with dynamic control after 6, 12 and 36 months showed the effectiveness of such surgical intervention with results comparable to the world indicators of leading clinics.
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促肾上腺皮质激素(ACTH)产生的神经内分泌肺肿瘤患者的准备和手术治疗特点
背景:以A.V.Vishnevsky命名的国家外科医学研究中心胸外科20多年来一直在处理神经内分泌肺肿瘤患者的手术治疗问题。本文介绍了15年来治疗异位ACTH综合征的经验。目的:研究支气管肺局限性ACTH产生肿瘤的准备特点、手术治疗和延迟疗效。材料和方法:该研究包括2005年至2020年期间接受支气管肺定位ACTH产生神经内分泌肿瘤手术治疗的55名患者。为了使手术治疗方法和手术类型的选择系统化,对患者的严重程度进行了点分析。分析了患者的人口学信息、记忆数据、术前和术后阶段的激素和仪器研究结果以及长期治疗结果。患者术后观察的控制期为6个月至5年。结果:患者年龄18~72岁(36±15)。根据胸部的MSCT结果,在肺部检测到大小从5到25毫米不等的肿瘤。评分在18-23分之间的患者因病情严重而进行了肺切除术。在总分为14至18分的情况下,进行了带淋巴结清扫的节段切除术。当总分小于14分时,进行肺叶切除术并进行淋巴结清扫。在计划的组织学检查中,所有患者都确认了不同分化程度的肺神经内分泌肿瘤。治疗结果随访时间为6至60个月,中位数为19个月[10;24]。83%的患者在动态随访1年后发现皮质醇增多症的临床表现消退。经过60个月的随访,10名患者(71.4%)在手术治疗后具有持续的临床效果,皮质醇增多症症状完全消退。结论:根据所提出的方法论方面,在6个月、12个月和36个月后进行动态控制,对手术治疗的结果进行分析,显示了这种手术干预的有效性,其结果与世界领先诊所的指标相当。
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