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Definitive radiotherapy for inoperable adenoid cystic carcinoma of the trachea: A rare case report

机译:不可手术的气管腺样囊性癌的明确放疗:罕见病例报告

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Adenoid cystic carcinoma (ACC) of the trachea is rare; it represents 1% of all respiratory tract cancers. It is generally considered as a slow-growing, with prolonged clinical course. Most patients present with dyspnea, and the symptoms often mimic those of asthma or chronic bronchitis. Surgical resection is the mainstay of treatment often combined to radiotherapy because of close surgical margins. When surgery is not possible, most tumors respond to radiotherapy alone which often results in long periods of remission. There is no consensus on the best treatment for locally advanced inoperable ACC of trachea. This case report describes a 51-year-old woman unresectable ACC of trachea due to comorbid conditions, successfully managed by intensity modulated radiotherapy. At 8 months follow-up, the patient is healthy and asymptomatic.
机译:气管腺样囊性癌(ACC)很少见;它占所有呼吸道癌症的1%。它通常被认为是生长缓慢,具有延长的临床过程。大多数患者出现呼吸困难,症状通常类似于哮喘或慢性支气管炎。手术切除是治疗的主要手段,由于狭窄的手术切缘,通常将其与放疗结合使用。当不可能进行手术时,大多数肿瘤仅对放射疗法有反应,这通常会导致长期缓解。对于局部晚期不能手术的气管ACC的最佳治疗方法尚无共识。该病例报告描述了一名51岁女性因合并症而无法切除的气管ACC,通过调强放疗成功地对其进行了治疗。在8个月的随访中,该患者健康无症状。

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