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

IF 0.6 Q4 OBSTETRICS & GYNECOLOGY
Case Reports in Obstetrics and Gynecology Pub Date : 2022-07-31 eCollection Date: 2022-01-01 DOI:10.1155/2022/3234784
Saki Yamamoto, Tomohiro Kikuchi, Hiroyuki Fujii, Yuko Otake, Mitsuru Matsuki, Risa Narumi, Masashi Endo, Hiroyuki Fujiwara, Harushi Mori
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引用次数: 1

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.

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1例破裂的去个体化卵巢子宫内膜瘤:序列MRI对确定适当治疗的有用性。
妊娠期血清孕酮水平升高可引起卵巢子宫内膜瘤的脱个体化,超声检查显示类似恶性肿瘤。此外,去个体化卵巢子宫内膜瘤在妊娠期间可能破裂并引起急性腹痛。据报道,磁共振成像(MRI)可用于区分卵巢子宫内膜异位瘤和恶性肿瘤。然而,据我们所知,脱个体化卵巢子宫内膜异位瘤破裂前后的连续MRI检查尚未见报道。在此,我们报告的情况下,39岁的妇女与破裂的去个体化卵巢子宫内膜异位瘤,其中连续MRI是有用的适当的管理。她有右卵巢子宫内膜异位瘤病史。妊娠20周经阴道超声检查显示已知右侧卵巢子宫内膜瘤伴壁结节,妊娠前不明显。进一步的MRI检查显示卵巢子宫内膜异位瘤伴壁结节,信号与胎盘相似。根据MRI检查结果,我们诊断为卵巢去个体化子宫内膜瘤。在怀孕27周时,她主诉突然腹痛,为此进行了MRI检查。MRI显示卵巢子宫内膜异位瘤消失并伴有血性腹水,据此诊断为卵巢子宫内膜异位瘤破裂。腹痛立即消退,并采取保守观察治疗。妊娠37周,右侧卵巢膀胱切除术与选择性剖宫产术同时进行,发现卵巢去个体化子宫内膜瘤破裂。我们的研究结果表明,在连续MRI上准确诊断破裂的去个体化卵巢子宫内膜异位瘤有助于其治疗。
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来源期刊
Case Reports in Obstetrics and Gynecology
Case Reports in Obstetrics and Gynecology Medicine-Obstetrics and Gynecology
CiteScore
1.30
自引率
0.00%
发文量
64
审稿时长
12 weeks
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