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本文引用的文献

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Primary pulmonary malignant fibrous histiocytoma.原发性肺恶性纤维组织细胞瘤
Case Rep Pulmonol. 2015;2015:381276. doi: 10.1155/2015/381276. Epub 2015 Mar 8.
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Endobronchial malignant fibrous histiocytoma: case report of an unusual presentation and palliative flexible bronchoscopic resection.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。
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原发性肺恶性纤维组织细胞瘤

Primary Pulmonary Malignant Fibrous Histiocytoma.

作者信息

Coşgun Tuğba, Tezel Yelda, Akyıl Mustafa, Kolbaş İlker, Şen Ayçım, Tezel Çağatay

机构信息

Department of Thoracic Surgery, Acıbadem University Atakent Hospital, İstanbul, Turkey.

Clinic of Chest Diseases, Haydarpaşa Training Hospital, İstanbul, Turkey.

出版信息

Turk Thorac J. 2017 Apr;18(2):54-56. doi: 10.5152/TurkThoracJ.2017.16039. Epub 2017 Mar 1.

DOI:10.5152/TurkThoracJ.2017.16039
PMID:29404161
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5783081/
Abstract

Malignant fibrous histiocytoma (MFH) cases are classified within the group of nonclassified sarcomas. The etiopathogenesis is unclear; however, MFH commonly develops in scar tissue and in areas exposed to radiation. MFH is the most common soft tissue sarcoma in adults and may be borne in the lungs, chest wall, mediastinum, or other tissues. Primary MFH of the lung constitutes less than 0.2% of all pulmonary neoplasms; thus, an optimal treatment strategy has not yet been elucidated. We aimed to report a case of MFH of the lung with subsequent treatment administration.

摘要

恶性纤维组织细胞瘤（MFH）病例归类于未分类肉瘤组。其病因发病机制尚不清楚；然而，MFH通常发生于瘢痕组织以及接受过辐射的区域。MFH是成人中最常见的软组织肉瘤，可发生于肺、胸壁、纵隔或其他组织。原发性肺MFH占所有肺部肿瘤的比例不到0.2%；因此，尚未阐明最佳治疗策略。我们旨在报告一例肺MFH病例及后续的治疗情况。