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Der Granularzelltumor der Luftwege – eine seltene Tumorentit?t

机译:气道颗粒细胞瘤-一种罕见的肿瘤实体

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Introduction: Pulmonary lesions are often detected in routine x-rays, leading to a more invasive diagnostic pathway. Occasionally rare tumor entities are encountered. Case report: We report a patient, who had a check-up where chest x-ray showed a pulmonary lesion. The following CT imaging confirmed the suspicion. On bronchoscopy multiple endobronchial lesions were found. The initial pulmonaly lesion was confirmed in a puncture as a chondrohamartoma. The larger endobronchial lesions were surgically resected and diagnosed as granular cell tumours. Postoperative controlls excluded a recurrence and the ones left in place showed no progression. Conclusion: The granular cell tumour of the lung is a rare tumour entity mainly reported as a case report. Optimal therapy of these mostly accidentally found tumours is either bronchoscopical or surgical resection, both therapies showing the same results. The lesions are mainly benign. For the few patients with a follow-up no recurrence has been reported. Due to the benign histology and the excellent prognosis no further treatment is required.
机译:简介:肺部病变通常在常规X射线检查中发现,从而导致更具侵入性的诊断途径。偶尔会遇到罕见的肿瘤实体。病例报告:我们报告了一名患者,该患者接受了检查,胸部X线显示有肺部病变。随后的CT成像证实了怀疑。支气管镜检查发现多支气管内病变。最初的肺部病变经穿刺证实为软骨瘤。手术切除较大的支气管内病变,并诊断为粒状细胞瘤。术后控制排除了复发,而留在原处的则没有进展。结论:肺颗粒细胞瘤是一种罕见的肿瘤实体,主要报道为一例。这些最偶然发现的肿瘤的最佳治疗方法是支气管镜或手术切除,两种疗法显示出相同的结果。病变主要是良性的。对于少数接受随访的患者,没有复发的报道。由于组织学良好且预后良好,因此无需进一步治疗。

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