气管支气管软骨发育不良并发肺腺癌:罕见病例报告。

IF 0.5 4区 医学 Q4 SURGERY
Zhang Guoliang, Zhang Zefeng, Zhu Qikun, Mi Lili, Wang Rui
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引用次数: 0

摘要

一名 67 岁的女性患者一个月前因体检发现肺部结节而就诊。通过胸部计算机断层扫描、支气管镜检查和活检标本的病理检查,她被诊断为气管支气管软骨发育不良并发右下叶结节。我们通过视频辅助胸腔镜手术进行了肺叶和淋巴结切除术,肺部小病灶被诊断为肺腺癌。在 36 个月的随访中,患者没有复发。总之,气管支气管骨软骨发育不全并发肺腺癌的情况非常罕见,临床医生应注意这种可能性,尤其是肺部恶性肿瘤患者和胸部影像学显示气管不规则的患者。否则,气管支气管软骨发育不全很容易被误诊为气管恶性肿瘤。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Tracheobronchopathia osteochondroplastica complicated with a pulmonary adenocarcinoma: A rare case report.

A 67-year-old female patient presented with a lung nodule one month ago which was detected by physical examination. She was diagnosed with tracheobronchopathia osteochondroplastica complicated with right lower lobe nodules by chest computed tomography, bronchoscopy, and pathological examinations of the biopsy specimens. We performed lobectomy and lymphadenectomy by video-assisted thoracoscopic surgery and small pulmonary lesions were diagnosed as pulmonary adenocarcinomas. At 36 months of follow-up, the patient was free from recurrence. In conclusion, tracheobronchopathia osteochondroplastica complicated with a pulmonary adenocarcinoma is rare, and clinicians should be aware of this possibility, particularly in patients with pulmonary malignancy and tracheal irregularities on chest imaging. Otherwise, tracheobronchopathia osteochondroplastica can be easily misdiagnosed as malignant invasion of the trachea.

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来源期刊
CiteScore
1.00
自引率
0.00%
发文量
98
审稿时长
3-8 weeks
期刊介绍: The Turkish Journal of Thoracic and Cardiovascular Surgery is an international open access journal which publishes original articles on topics in generality of Cardiac, Thoracic, Arterial, Venous, Lymphatic Disorders and their managements. These encompass all relevant clinical, surgical and experimental studies, editorials, current and collective reviews, technical know-how papers, case reports, interesting images, How to Do It papers, correspondences, and commentaries.
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