Schumacher A, Saile G, Brühwiler H, Lüscher K P
Frauenklinik Kaontonsspital Münsterlingen.
Geburtshilfe Frauenheilkd. 1995 Oct;55(10):602-4. doi: 10.1055/s-2007-1023533.
A 49-year-old woman presented with a uterine tumour with solid and cystic parts. Extension of the tumour into the broad ligament was noted at the operation with wormlike plugs of tumour within the veins. The histological diagnosis of intravenous leiomyomatosis was evident. The disease turned out to be far advanced: a long continuous intraluminal mass extending from the iliac veins to the right ventricle made a second operation with thoracotomy and laparotomy mandatory. Postoperative follow-up showed so far, 1.5 years after operation, no evidence of recurrence. Intravenous leiomyomatosis is a very uncommon finding. Though it is histologically a benign smooth-muscle tumour, the biological behaviour with intravenous growth which may involve the right side of the heart, is quite aggressive. About 100 cases were reported in the literature; in no case could the diagnosis be made before surgery.
一名49岁女性因子宫肿瘤伴实性和囊性成分就诊。手术中发现肿瘤延伸至阔韧带,静脉内可见蠕虫状肿瘤栓子。静脉内平滑肌瘤病的组织学诊断明确。结果显示病情已进展至晚期:一个从髂静脉延伸至右心室的长段连续腔内肿块使得必须进行第二次开胸和剖腹手术。术后随访至今,术后1.5年,无复发迹象。静脉内平滑肌瘤病是一种非常罕见的病症。尽管其在组织学上是良性平滑肌肿瘤,但其静脉内生长的生物学行为可能累及心脏右侧,颇具侵袭性。文献报道约100例;术前均无法做出诊断。