日本産科婦人科内視鏡学会雑誌
Online ISSN : 1884-5746
Print ISSN : 1884-9938
症例報告
腹腔鏡下子宮筋腫核出術後4年後、偶発的に発見された静脈内平滑筋腫症の1例
工藤 友希乃渡辺 正黒澤 大樹虎谷 惇平渡部 洋渡辺 徹雄
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2025 年 41 巻 1 号 p. 103-108

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 Intravenous leiomyomatosis (IVL) is a rare disorder among benign leiomyomas, which may arise from uterine myoma or smooth muscle of the vessel wall, extend into the veins. It sometimes extends into the inferior vena cava or the right atrium, causing a serious condition that can lead to sudden death. A 32-year-old nulliparous woman underwent laparoscopic myomectomy for a degenerative myoma. Four years after the surgery, an indistinct borderline mass appeared in the uterine body, for which the possibility of a degenerative myoma or sarcoma could not be ruled out. After preoperative blood tests, contrast-enhanced CT scan, and MRI, total hysterectomy was performed. Intraoperatively, an elastic hard mass was palpated in the left ovarian adnexal vessels, and when the vessels were cut open to examine the interior, a leiomyoma-like mass was confirmed grossly. Suspecting IVL or another disease extending into the left ovarian adnexa, a left adnexectomy was additionally performed for diagnosis and to prevent dispersal of the embolus. Postoperative contrast-enhanced CT scan and a reexamination of the preoperative imaging studies revealed shadow defects in the iliac vein, the left renal vein, the inferior vena cava, and the right pulmonary artery. The patient was transferred to another hospital for tumor embolization in the inferior vena cava and iliac vein, bilateral ovarian vein ligation, bilateral internal iliac vein ligation, and right ovariectomy, and the diagnosis of IVL was confirmed.

 Although intravenous leiomyomatosis is a rare disease, imaging and consultation with the possibility of its occurrence in mind may lead to early intervention.

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