{"title":"上皮样滋养细胞肿瘤的特征:内窥镜和磁共振成像发现。","authors":"Daiki Idegami, Tsukuru Amano, Hiroko Torii, Shunichiro Tsuji, Mamoru Urabe, Takashi Murakami","doi":"10.1159/000539428","DOIUrl":null,"url":null,"abstract":"<p><strong>Introduction: </strong>Epithelioid endothelial tumor (ETT) is an extremely rare tumor that typically occurs in women of reproductive age. The diagnosis tends to be delayed because it often necessitates a total hysterectomy. Therefore, it is important to understand ETT macroscopic and imaging findings. Here, we report a case of ETT with detailed macroscopic and imaging findings.</p><p><strong>Case presentation: </strong>A 39-year-old woman with positive pregnancy test results was admitted to a nearby hospital. No gestational sac was found in the uterus, and magnetic resonance imaging (MRI) revealed a cystic mass of approximately 7 cm that extended continuously from the anterior wall of the lower uterine segment into the pelvic cavity. She underwent laparoscopic and hysteroscopic surgeries for a ruptured cervical pregnancy. Pathology of the specimens obtained from this surgery did not allow for the diagnosis of ETT. Two months after the surgery, as the serum human chorionic gonadotropin β subunit (β-HCG) level did not decrease, she was diagnosed with low-grade gestational trophoblastic neoplasia, leading to the administration of chemotherapy. After three regimens of chemotherapy over 9 months, her β-HCG level decreased but did not reach normal levels. Ultimately, a total hysterectomy was performed. The pathological diagnosis was mixed ETT and choriocarcinoma. A literature review revealed several cases similar to ours.</p><p><strong>Conclusion: </strong>ETT in the lower uterus often perforates the myometrium and forms cystic lesions in the retroperitoneal space or subserosa. The MRI and laparoscopic/hysteroscopic findings in this case may have contributed to the early diagnosis of ETT.</p>","PeriodicalId":9625,"journal":{"name":"Case Reports in Oncology","volume":"17 1","pages":"666-672"},"PeriodicalIF":0.7000,"publicationDate":"2024-06-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11250665/pdf/","citationCount":"0","resultStr":"{\"title\":\"Characteristics of Epithelioid Trophoblastic Tumor: Endoscopic and Magnetic Resonance Imaging Findings.\",\"authors\":\"Daiki Idegami, Tsukuru Amano, Hiroko Torii, Shunichiro Tsuji, Mamoru Urabe, Takashi Murakami\",\"doi\":\"10.1159/000539428\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Introduction: </strong>Epithelioid endothelial tumor (ETT) is an extremely rare tumor that typically occurs in women of reproductive age. The diagnosis tends to be delayed because it often necessitates a total hysterectomy. Therefore, it is important to understand ETT macroscopic and imaging findings. Here, we report a case of ETT with detailed macroscopic and imaging findings.</p><p><strong>Case presentation: </strong>A 39-year-old woman with positive pregnancy test results was admitted to a nearby hospital. No gestational sac was found in the uterus, and magnetic resonance imaging (MRI) revealed a cystic mass of approximately 7 cm that extended continuously from the anterior wall of the lower uterine segment into the pelvic cavity. She underwent laparoscopic and hysteroscopic surgeries for a ruptured cervical pregnancy. Pathology of the specimens obtained from this surgery did not allow for the diagnosis of ETT. Two months after the surgery, as the serum human chorionic gonadotropin β subunit (β-HCG) level did not decrease, she was diagnosed with low-grade gestational trophoblastic neoplasia, leading to the administration of chemotherapy. After three regimens of chemotherapy over 9 months, her β-HCG level decreased but did not reach normal levels. Ultimately, a total hysterectomy was performed. The pathological diagnosis was mixed ETT and choriocarcinoma. A literature review revealed several cases similar to ours.</p><p><strong>Conclusion: </strong>ETT in the lower uterus often perforates the myometrium and forms cystic lesions in the retroperitoneal space or subserosa. 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引用次数: 0
摘要
简介上皮样内皮肿瘤(ETT)是一种极为罕见的肿瘤,通常发生在育龄妇女身上。由于往往需要进行全子宫切除术,因此诊断往往被延误。因此,了解 ETT 的宏观和影像学表现非常重要。在此,我们报告了一例 ETT 病例,并提供了详细的宏观和影像学检查结果:一名妊娠试验阳性的 39 岁女性住进了附近的一家医院。子宫内未发现妊娠囊,磁共振成像(MRI)显示有一个约 7 厘米的囊性肿块,从子宫下段前壁连续延伸至盆腔。她因宫颈妊娠破裂接受了腹腔镜和宫腔镜手术。手术标本的病理结果无法确诊为 ETT。手术两个月后,由于血清中人绒毛膜促性腺激素β亚基(β-HCG)水平没有下降,她被诊断为低度妊娠滋养细胞肿瘤,因此接受了化疗。经过 9 个月的三次化疗,她的β-HCG 水平有所下降,但仍未达到正常水平。最终,她接受了全子宫切除术。病理诊断为混合型 ETT 和绒毛膜癌。文献综述显示有几例与我们的病例类似:结论:子宫下段的ETT通常会穿破子宫肌层,在腹膜后间隙或粘膜下形成囊性病变。本病例的磁共振成像和腹腔镜/宫腔镜检查结果可能有助于ETT的早期诊断。
Characteristics of Epithelioid Trophoblastic Tumor: Endoscopic and Magnetic Resonance Imaging Findings.
Introduction: Epithelioid endothelial tumor (ETT) is an extremely rare tumor that typically occurs in women of reproductive age. The diagnosis tends to be delayed because it often necessitates a total hysterectomy. Therefore, it is important to understand ETT macroscopic and imaging findings. Here, we report a case of ETT with detailed macroscopic and imaging findings.
Case presentation: A 39-year-old woman with positive pregnancy test results was admitted to a nearby hospital. No gestational sac was found in the uterus, and magnetic resonance imaging (MRI) revealed a cystic mass of approximately 7 cm that extended continuously from the anterior wall of the lower uterine segment into the pelvic cavity. She underwent laparoscopic and hysteroscopic surgeries for a ruptured cervical pregnancy. Pathology of the specimens obtained from this surgery did not allow for the diagnosis of ETT. Two months after the surgery, as the serum human chorionic gonadotropin β subunit (β-HCG) level did not decrease, she was diagnosed with low-grade gestational trophoblastic neoplasia, leading to the administration of chemotherapy. After three regimens of chemotherapy over 9 months, her β-HCG level decreased but did not reach normal levels. Ultimately, a total hysterectomy was performed. The pathological diagnosis was mixed ETT and choriocarcinoma. A literature review revealed several cases similar to ours.
Conclusion: ETT in the lower uterus often perforates the myometrium and forms cystic lesions in the retroperitoneal space or subserosa. The MRI and laparoscopic/hysteroscopic findings in this case may have contributed to the early diagnosis of ETT.