Suppr超能文献

[静脉内平滑肌瘤病伴心脏内扩展:一例报告]

[Intravenous leiomyomatosis with intracardiac extension: a case report].

作者信息

Zhang Tao, Zhang Xiao Ming, Zhang Xue Min, Li Qing Le

机构信息

Department of Vascular Surgery, Peking University People's Hospital, Beijing, China.

出版信息

Beijing Da Xue Xue Bao Yi Xue Ban. 2008 Dec 18;40(6):642-4.

Abstract

Intravenous leiomyomatosis is characterized by a proliferation of benign smooth muscular tissue growing into uterine with malignant appearance. On extremely rare occasions, the tumor may grow out of the pelvis and extend into the inferior vena cava and the right atrium. We report a case of intravenous leiomyomatosis extending into the right atrium. A 41-year-old woman complained of 20 days of intermittent abdominal pain and lower limbs swell. Medical history of the patient revealed a previous hysterectomy operation 3 years ago due to uterine leiomyoma. Echocardiography showed a homogenous mass extending from the inferior vena cava to the right atrium, without evidence of adherence to the right atrial wall, the left ventricular ejection fraction was only 60%. Computer tomography showed that a large mass arising from the left internal iliac vein and extending into the right chambers. Pelvic vascular ultrasound revealed the thrombotic material in the inferior vena cava and the left common iliac vein, and confirmed the presence of a complex mass in the left annex region. Based on the findings, the initial diagnosis was intracardiac and intravenous tumor. An operation was performed through a sternotomy and laparotomy to remove the whole tumor from the left common iliac vein to the right atrium, ligate left internal iliac vein mean-wile. No hormonal therapy was administrated after the operation. Immunohistochemical studies revealed that the tumor cells were fusiform shape, there was no karyokinesis and necrosis, and the tumor cells were positive for smooth muscle antigen and desmin, as well as estrogen receptor and progesterone receptor. Six months postoperation follow-up revealed no signs of recurrence. The differential diagnosis of the disease compared with primary cardiovascular sarcomas and thrombus was difficult. The final diagnosis relied on immunohistochemical analysis, however, the short-term result of operation was acceptable.

摘要

静脉内平滑肌瘤病的特征是良性平滑肌组织增生并长入子宫,外观呈恶性。在极少数情况下,肿瘤可能会生长出盆腔并延伸至下腔静脉和右心房。我们报告一例静脉内平滑肌瘤病延伸至右心房的病例。一名41岁女性主诉间歇性腹痛20天及下肢肿胀。患者病史显示3年前因子宫肌瘤行子宫切除术。超声心动图显示一个均匀的肿块从下腔静脉延伸至右心房,无附着于右心房壁的证据,左心室射血分数仅为60%。计算机断层扫描显示一个大肿块起源于左髂内静脉并延伸至右心房。盆腔血管超声显示下腔静脉和左髂总静脉内有血栓物质,并证实左附件区存在一个复杂肿块。根据这些发现,初步诊断为心内和静脉内肿瘤。通过胸骨切开术和剖腹术进行手术,从左髂总静脉至右心房切除整个肿瘤,同时结扎左髂内静脉。术后未给予激素治疗。免疫组织化学研究显示肿瘤细胞呈梭形,无核分裂象和坏死,肿瘤细胞平滑肌抗原、结蛋白、雌激素受体和孕激素受体均呈阳性。术后6个月随访未发现复发迹象。该疾病与原发性心血管肉瘤和血栓的鉴别诊断困难。最终诊断依赖于免疫组织化学分析,然而,手术的短期结果是可以接受的。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验