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一例蜕膜化卵巢子宫内膜异位囊肿破裂病例:系列磁共振成像在确定适当治疗方案中的应用价值

A Case of Ruptured Decidualized Ovarian Endometrioma: Usefulness of Serial MRI for Determining Adequate Management.

作者信息

Yamamoto Saki, Kikuchi Tomohiro, Fujii Hiroyuki, Otake Yuko, Matsuki Mitsuru, Narumi Risa, Endo Masashi, Fujiwara Hiroyuki, Mori Harushi

机构信息

Department of Radiology, Jichi Medical University School of Medicine, Tochigi, Japan.

Department of Obstetrics and Gynecology, Jichi Medical University School of Medicine, Tochigi, Japan.

出版信息

Case Rep Obstet Gynecol. 2022 Jul 31;2022:3234784. doi: 10.1155/2022/3234784. eCollection 2022.

Abstract

Decidualization can originate in ovarian endometrioma by elevated serum progesterone levels during pregnancy, which mimics malignancy on ultrasonography. Moreover, decidualized ovarian endometrioma may rupture and cause acute abdominal pain during pregnancy. Magnetic resonance imaging (MRI) is reportedly useful in differentiating decidualized ovarian endometriomas from malignancies. However, to our knowledge, serial MRI of decidualized ovarian endometrioma before and after rupture has not been reported. Herein, we report the case of a 39-year-old woman with a ruptured decidualized ovarian endometrioma in which serial MRI was useful for adequate management. She had a history of right ovarian endometrioma. Transvaginal ultrasonography at 20 weeks of gestation showed the known right ovarian endometrioma with mural nodules that were not evident before pregnancy. MRI for further evaluation showed ovarian endometrioma with mural nodules with signals similar to those of the placenta. Based on the MRI findings, we diagnosed a decidualized ovarian endometrioma. At 27 weeks of gestation, she complained of sudden abdominal pain, for which MRI was performed. MRI showed disappearance of the ovarian endometrioma and bloody ascites, based on which we diagnosed a ruptured ovarian endometrioma. The abdominal pain subsided immediately, and a conservative observational treatment approach was taken. At 37 weeks of gestation, right ovarian cystectomy was performed simultaneously with an elective cesarean section, which revealed a ruptured decidualized ovarian endometrioma. Our findings demonstrate that the accurate diagnosis of a ruptured decidualized ovarian endometrioma on serial MRI can contribute to its management.

摘要

蜕膜化可因孕期血清孕酮水平升高而起源于卵巢子宫内膜异位囊肿,在超声检查中表现类似恶性肿瘤。此外,蜕膜化的卵巢子宫内膜异位囊肿在孕期可能破裂并引起急性腹痛。据报道,磁共振成像(MRI)有助于鉴别蜕膜化的卵巢子宫内膜异位囊肿与恶性肿瘤。然而,据我们所知,尚未有关于蜕膜化卵巢子宫内膜异位囊肿破裂前后的系列MRI报道。在此,我们报告一例39岁患有破裂的蜕膜化卵巢子宫内膜异位囊肿的女性病例,其中系列MRI有助于进行恰当的处理。她有右侧卵巢子宫内膜异位囊肿病史。妊娠20周时经阴道超声检查显示已知的右侧卵巢子宫内膜异位囊肿伴有壁结节,这些壁结节在妊娠前并不明显。为进一步评估而进行的MRI显示卵巢子宫内膜异位囊肿伴有壁结节,其信号与胎盘相似。基于MRI表现,我们诊断为蜕膜化卵巢子宫内膜异位囊肿。妊娠27周时,她主诉突发腹痛,为此进行了MRI检查。MRI显示卵巢子宫内膜异位囊肿消失及血性腹水,据此我们诊断为卵巢子宫内膜异位囊肿破裂。腹痛立即缓解,遂采取保守观察治疗方法。妊娠37周时,在择期剖宫产的同时行右侧卵巢囊肿切除术,术中发现为破裂的蜕膜化卵巢子宫内膜异位囊肿。我们的研究结果表明,通过系列MRI准确诊断破裂的蜕膜化卵巢子宫内膜异位囊肿有助于其治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d29/9357808/d40ab91c647f/CRIOG2022-3234784.001.jpg

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