The frequency of lung cancer in patients with pulmonary hamartomas: An evaluation of clinical, radiological, and pathological features and follow-up data of 96 patients with pulmonary hamartomas

G.H. Ekinci , O. Hacıömeroğlu , A. Ersev , L. Alpay , H. Özgen , A. Yılmaz
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引用次数: 12

Abstract

Purpose

To investigate the frequency of lung cancer in patients with pulmonary hamartomas and to evaluate clinical, radiological, and pathological characteristics of pulmonary hamartomas.

Basic procedures

We reviewed pathology records of pulmonary hamartomas diagnosed between 2003 and 2014. Medical records and the hospital electronic database were also reviewed for each patient to obtain clinical, radiological, and pathological characteristics of pulmonary hamartomas and accompanying malignancies.

Main findings

Ninety-six patients with pulmonary hamartomas were identified. There were 26 females (27%) and 70 males (73%), with a mean age of 56.2 years (range 22–87 years). Malignancies were detected in 23 patients (24%), which developed previously in five patients (1 synchronous, 4 metachronous lesions), and concomitantly in 18 patients (with origin from the lung in 17 patients and from the pleura in 1 patient).

Principal conclusions

Our results show that patients with pulmonary hamartomas may have coexisting lung malignancies.

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肺错构瘤患者肺癌的发生频率:96例肺错构瘤患者的临床、影像学、病理特征及随访资料的评价
目的探讨肺错构瘤患者发生肺癌的频率,探讨肺错构瘤的临床、影像学和病理特点。我们回顾了2003年至2014年间诊断的肺错构瘤的病理记录。我们还查阅了每位患者的医疗记录和医院电子数据库,以获得肺错构瘤及其伴随的恶性肿瘤的临床、放射学和病理特征。主要发现肺错构瘤96例。女性26例(27%),男性70例(73%),平均年龄56.2岁(22 ~ 87岁)。23例患者(24%)检测到恶性肿瘤,其中5例患者(1例同步病变,4例异时病变)发生过恶性肿瘤,18例患者伴有恶性肿瘤(17例起源于肺部,1例起源于胸膜)。结论肺错构瘤患者可能同时存在肺部恶性肿瘤。
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