Mazzola A, Gregorini R, Procaccini B, Moretti V, Lucantoni R, Lorenzi W, Di Eusanio G, Colombati M
Department of Cardiac Surgery, Ospedale Civile, Teramo, Italy.
Ann Vasc Surg. 1986 May;1(1):134-8. doi: 10.1016/S0890-5096(06)60715-2.
Intracaval leiomyomatosis of uterine origin is a rare disease. Extension to the right heart is exceptional. Based on the review of 11 cases reported in the literature and the case presented herein, which was treated successfully, the diagnostic and therapeutic problems are discussed. Diagnosis should be suggested when a female patient operated on previously for myofibroma of the uterus by hysterectomy, presents with a picture of cardiac myxoma. Diagnosis can be confirmed by iliocavogram and computerized tomography of the abdomen. Excision calls for a cardiac procedure under extracorporeal circulation and caval exploration which may be performed either simultaneously or as a two stage procedure.
起源于子宫的腔静脉平滑肌瘤病是一种罕见疾病。延伸至右心的情况极为罕见。基于对文献报道的11例病例以及本文所呈现的成功治疗病例的回顾,对诊断和治疗问题进行了讨论。当一名曾因子宫肌纤维瘤接受子宫切除术的女性患者出现心脏黏液瘤的症状时,应考虑诊断。通过髂腔静脉造影和腹部计算机断层扫描可确诊。切除需要在体外循环下进行心脏手术并探查腔静脉,可同时进行或分两阶段进行。