原发性心脏肉瘤：约2例。
Primitive cardiac sarcomas: about 2 cases.
作者信息
Jerbi Sofiane, Romdhani Noureddine, Tarmiz Amine, Mlika Sinane, Nizar Khelil, Beltaïfa Mohamed, Belghith Makhlouf, Limayem Faouzi, Ennabli Kamel
机构信息
Cardio-vascular and thoracic department, Sahloul University Hospital, Sousse, Tunisia.
出版信息
Tunis Med. 2007 Nov;85(11):960-2.
BACKGROUND
the cardiac sarcomas, although very rare, represent the quasi-totality of the primitive sly tumors of the heart
AIM
it is about a retrospective study of two cases of cardiac sarcomas operated in Sahloul university hospital of Sousse.
CASES
it is about a woman and a man: The respective ages were 22 and 45 years. The clinical pattern of the patients was polymorphic and the diagnosis put by cardiac echography. Both patients had a surgical resection and a chemotherapy. Both patients died in 13 and 18 months after the diagnosis.
CONCLUSION
because of the extreme rarity of the cardiac sarcomas, there is no precise therapeutic strategy. The only consensus concerns the surgery as soon as the diagnosis of cardiac tumor is put. The prognosis of these tumors is extremely redoubtable with a survival which does not exceed 2 years after the beginning of the symptomatology.
背景
心脏肉瘤虽然非常罕见，但几乎是心脏原发性恶性肿瘤的全部。
目的
这是一项对在苏塞的萨赫卢勒大学医院接受手术的两例心脏肉瘤病例的回顾性研究。
病例
一名女性和一名男性，年龄分别为22岁和45岁。患者的临床症状多样，通过心脏超声检查做出诊断。两名患者均接受了手术切除和化疗。两名患者在诊断后13个月和18个月死亡。
结论
由于心脏肉瘤极为罕见，尚无精确的治疗策略。唯一的共识是一旦诊断出心脏肿瘤就应尽快进行手术。这些肿瘤的预后极差，出现症状后生存期不超过2年。
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