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支气管内恶性纤维组织细胞瘤:一种不常见表现病例报告和姑息性纤维支气管镜切除术。

Endobronchial malignant fibrous histiocytoma: case report of an unusual presentation and palliative flexible bronchoscopic resection.

机构信息

Division of Pulmonary and Critical Care Medicine, Department of Internal Medicine, CHA Bundang Medical Center, College of Medicine, CHA University, Seongnam, South Korea.

出版信息

Respir Care. 2013 Aug;58(8):e92-4. doi: 10.4187/respcare.01996. Epub 2012 Dec 18.

Abstract

Primary malignant fibrous histiocytoma (MFH) of the lung is a very rare neoplasm that usually presents as a parenchymal mass. Here we report an unusual case of primary MFH of the bronchus, showing relatively benign clinical features. We performed a palliative resection via flexible bronchoscopy, using a polypectomy snare. The patient has survived for over 2 years after being diagnosed with an endobronchial mass, later found to be MFH, and 14 months post-debulking. There is a possibility that endobronchial MFH has a more favorable prognosis than MFH of other origins. If this is true, interventional bronchoscopy can be a reasonable option for non-operable cases of MFH.

摘要

原发性肺恶性纤维组织细胞瘤(MFH)是一种非常罕见的肿瘤,通常表现为实质肿块。在此,我们报告一例支气管原发性 MFH 的不典型病例,其表现出相对良性的临床特征。我们通过软性支气管镜使用息肉切除术圈套器进行姑息性切除。该患者在诊断为支气管内肿块(后证实为 MFH)后已生存超过 2 年,肿块减积术后 14 个月仍存活。支气管内 MFH 的预后可能优于其他起源的 MFH。如果这是真的,那么对于无法手术的 MFH 病例,介入性支气管镜检查可能是一种合理的选择。

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