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原发性纵隔平滑肌瘤:一例罕见病例报告及文献复习

Primary mediastinal leiomyoma: a rare case report and literature review.

作者信息

Li Chuan, Lin Feng, Pu Qiang, Liu Lunxu

机构信息

Department of Thoracic Surgery, West China Hospital, Sichuan University, Chengdu 610041, China.

出版信息

J Thorac Dis. 2018 Feb;10(2):E116-E119. doi: 10.21037/jtd.2018.01.37.

Abstract

Primary mediastinal leiomyomas are extremely rare, its etiology unknown, and up to the present has only been described in a few cases in the English literature. In this case report, we describe a 3-year-old girl with asymptomatic left upper quadrant abdominal mass. Chest computed tomography demonstrated a giant solid mass in the anterior mediastinum, which extended to the right hemi-thorax and left upper quadrant abdomen. Fortunately, the girl underwent a complete surgical tumor resection. The definitive diagnosis was primary mediastinal leiomyoma. To our best knowledge, this is the second case report of primary mediastinal leiomyoma of child.

摘要

原发性纵隔平滑肌瘤极为罕见,其病因不明,截至目前,英文文献中仅报道过少数病例。在本病例报告中,我们描述了一名3岁女童,其左上腹有一无症状肿块。胸部计算机断层扫描显示前纵隔有一个巨大实性肿块,延伸至右半胸和左上腹。幸运的是,该女童接受了肿瘤完整切除术。最终诊断为原发性纵隔平滑肌瘤。据我们所知,这是儿童原发性纵隔平滑肌瘤的第二例病例报告。

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引用本文的文献

本文引用的文献

1
Rare mediastinal leiomyoma in a child.儿童罕见的纵隔平滑肌瘤。
Gen Thorac Cardiovasc Surg. 2017 Jul;65(7):415-417. doi: 10.1007/s11748-016-0705-5. Epub 2016 Sep 17.
4
Primary mediastinal leiomyoma: a case report.原发性纵隔平滑肌瘤:一例报告
Cases J. 2009 Jul 16;2:8555. doi: 10.4076/1757-1626-2-8555.
5
A large leiomyoma of the mediastinum.纵隔巨大平滑肌瘤。
Br J Surg. 1954 Jan;41(168):446-7. doi: 10.1002/bjs.18004116833.
6
Mediastinal angioleiomyoma.纵隔血管平滑肌瘤。
Ann Thorac Surg. 2002 May;73(5):1653-4. doi: 10.1016/s0003-4975(01)03366-5.
10
Primary mediastinal leiomyoma.原发性纵隔平滑肌瘤。
Ann Thorac Surg. 1990 Aug;50(2):301-2. doi: 10.1016/0003-4975(90)90757-w.

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