A case of mediastinal angiosarcoma

被引:0
|
作者
Deroux, A. [1 ]
Destors, M. [1 ]
Coudurier, M. [1 ]
Lantuejoul, S. [2 ]
Aubert, M. [3 ]
Girard, N. [4 ]
Moro-Sibilot, D. [1 ]
机构
[1] CHU Grenoble, Unite Oncol Thorac, PCMAC, F-38043 Grenoble, France
[2] CHU Grenoble, Dept Anat & Cytol Pathol, F-38043 Grenoble, France
[3] Clin Belledonne, F-38400 St Martin Dheres, France
[4] Hosp Civils Lyon, Serv Pneumol, Unite Pilote Prise Charge Tumeurs Rares Intrathor, F-69229 Lyon 02, France
关键词
Angiosarcoma; Mediastinal tumour; Rare tumour; Surgery; SOFT-TISSUE;
D O I
10.1016/j.rmr.2012.04.009
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Introduction. - Mediastinal angiosarcoma is a rare intrathoracic tumour and the therapeutic approach remains poorly codified. Case report. - We report the case of a 65-year-old female patient presenting with chest pain. Further exploration revealed an anterior mediastinal mass with pericardial invasion. Transthoracic biopsy gave the diagnosis of angiosarcoma. Multimodal treatment with neoadjuvant chemotherapy (doxorubicin 20 mg/m(2), Ifosfamide 2500 mg/m(2), Uromitexan(R) 2500 mg/m(2)) and surgery followed by adjuvant radiotherapy has led to remission of the tumour that has persisted for 12 months. Conclusion. - Systematic recording of such conditions in dedicated registries could contribute to enhance the description of the clinical and pathological characteristics, thus helping define the principles of specific management. (C) 2012 SPLF. Published by Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:1120 / 1123
页数:4
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