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源于子宫平滑肌瘤的心脏内平滑肌瘤病——1例需要多学科剖腹术-开胸术治疗的罕见病例

Intracardiac Leiomyomatosis Arising from a Uterine Leiomyoma - A Rare Case Requiring a Multidisciplinary Laparotomy-Thoracotomy Approach.

作者信息

Murali T V, Thomas Reshma Sara, Pilllai Manjusha Narayana, Gopal Anitha

机构信息

Department of Surgical Oncology, Government Medical College, Kottayam, Kerala, India.

Department of Obstetrics and Gynecology, Government Medical College, Kottayam, Kerala, India.

出版信息

J Midlife Health. 2023 Jan-Mar;14(1):53-55. doi: 10.4103/jmh.jmh_47_23. Epub 2023 Jul 7.

Abstract

A 37-year-old lady, when being evaluated in gynecology for pain in the abdomen, was found to have a pelvic mass suspicious of ovarian cancer with markers negative. There was an ovarian vein thrombosis extending to the right atrium in the contrast-enhanced computed tomography scan. A fluorodeoxyglucose positron emission tomography-computed tomography ruled out any other lesions. The patient underwent surgery under general anesthesia with transesophageal echocardiography to monitor the atrial thrombus. Intraoperatively, a retroperitoneal mass is seen arising from the right adnexal region of the uterus extending to the lumbar area. After the hysterectomy, bilateral salpingo-oophorectomy, tumor resection, and baring and looping of the retroperitoneal vessels, a sternotomy was done, and she was put on cardiopulmonary bypass. The tumor thrombus had two limbs both arising from the mass, one through the ovarian and the second through the iliac veins and joining together inside the inferior vena cava (IVC). With the excision of the ovarian vein at its junction, atrial incision, and incisions over the iliac veins and IVC, the thrombus was removed completely in a single sitting. Final histopathology revealed intravenous leiomyomatosis and no malignancy. We report this case as a rare disease, with both ovarian and iliac thrombus being a further rarity and a multidepartment joint effort with a successful outcome.

摘要

一名37岁女性因腹部疼痛在妇科就诊时,被发现盆腔有一个可疑为卵巢癌的肿块,肿瘤标志物为阴性。在增强计算机断层扫描中发现卵巢静脉血栓延伸至右心房。氟脱氧葡萄糖正电子发射断层扫描-计算机断层扫描排除了任何其他病变。患者在全身麻醉下接受手术,并进行经食管超声心动图监测心房血栓。术中可见一个腹膜后肿块,起源于子宫右附件区并延伸至腰部区域。子宫切除、双侧输卵管卵巢切除、肿瘤切除以及腹膜后血管的显露和环扎后,进行了胸骨切开术,并对患者实施体外循环。肿瘤血栓有两个分支,均起源于肿块,一个通过卵巢静脉,另一个通过髂静脉,在腔静脉内汇合。在卵巢静脉与腔静脉交界处切除卵巢静脉、切开心房以及切开髂静脉和腔静脉后,一次性完整切除了血栓。最终组织病理学检查显示为静脉内平滑肌瘤病,无恶性病变。我们将此病例作为一种罕见疾病进行报告,同时存在卵巢和髂静脉血栓更是罕见,并且这是多科室共同努力取得成功结果的案例。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a81/10482015/41fea0f085f8/JMH-14-53-g001.jpg

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