{"title":"罕见的阔韧带肌瘤1例","authors":"Kamala Verma, Santosh Kumari","doi":"10.5005/jp-journals-10032-1168","DOIUrl":null,"url":null,"abstract":"Ab s t r Ac t Background: The broad ligament is the commonest extrauterine site for occurrence of leiomyoma. Because of its rarity, it poses both clinical and radiological difficulties in differentiating against an ovarian tumor. Case description: We are presenting a rare case of leiomyoma of broad ligament in a 45-year-old female with complaints of lower abdominal lump, pain, and menstrual abnormality. On clinical examination, there was a 18-week-old firm, nontender, and mobile mass extending to the umbilicus. Ultrasound pelvis showed a large hypoechoic lesion of 17 cm × 11 cm × 10.3 cm with internal vascularity in pelvis predominantly on the left side. MRI pelvis showed similar findings. IVP was normal. Result: Laparotomy showed a huge false left-sided broad ligament leiomyoma measuring 17 × 15 cm. Histopathology confirmed it to be a soft tissue tumor-leiomyoma. Conclusion: Broad ligament leiomyomas mimic ovarian tumors on clinical and radiological examination and may pose difficulties in differentiating both. Its diagnosis is difficult on clinical and radiological features owing to its unusual presentation. Thus histopathology plays an important role in confirming its diagnosis. Clinical significance: We present this case because of its rarity and the diagnostic difficulties it posed.","PeriodicalId":338227,"journal":{"name":"Journal of SAFOMS","volume":"629 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2019-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"3","resultStr":"{\"title\":\"A Rare Case of Broad Ligament Fibroid: A Case Report\",\"authors\":\"Kamala Verma, Santosh Kumari\",\"doi\":\"10.5005/jp-journals-10032-1168\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Ab s t r Ac t Background: The broad ligament is the commonest extrauterine site for occurrence of leiomyoma. Because of its rarity, it poses both clinical and radiological difficulties in differentiating against an ovarian tumor. Case description: We are presenting a rare case of leiomyoma of broad ligament in a 45-year-old female with complaints of lower abdominal lump, pain, and menstrual abnormality. On clinical examination, there was a 18-week-old firm, nontender, and mobile mass extending to the umbilicus. Ultrasound pelvis showed a large hypoechoic lesion of 17 cm × 11 cm × 10.3 cm with internal vascularity in pelvis predominantly on the left side. MRI pelvis showed similar findings. IVP was normal. Result: Laparotomy showed a huge false left-sided broad ligament leiomyoma measuring 17 × 15 cm. Histopathology confirmed it to be a soft tissue tumor-leiomyoma. Conclusion: Broad ligament leiomyomas mimic ovarian tumors on clinical and radiological examination and may pose difficulties in differentiating both. Its diagnosis is difficult on clinical and radiological features owing to its unusual presentation. Thus histopathology plays an important role in confirming its diagnosis. Clinical significance: We present this case because of its rarity and the diagnostic difficulties it posed.\",\"PeriodicalId\":338227,\"journal\":{\"name\":\"Journal of SAFOMS\",\"volume\":\"629 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2019-06-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"3\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of SAFOMS\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.5005/jp-journals-10032-1168\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of SAFOMS","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.5005/jp-journals-10032-1168","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 3
摘要
背景:阔韧带是子宫外平滑肌瘤最常见的发生部位。由于其罕见性,它在临床和放射学上都很难与卵巢肿瘤鉴别。病例描述:我们报告一例罕见的阔韧带平滑肌瘤病例,患者为45岁女性,主诉下腹肿块、疼痛和月经异常。在临床检查中,有一个18周大的坚固、无痛、可移动的肿块延伸到脐。骨盆超声示17 cm × 11 cm × 10.3 cm的大低回声病变,骨盆内血管主要位于左侧。骨盆MRI显示类似结果。IVP正常。结果:剖腹探查发现左侧宽韧带巨大假平滑肌瘤,大小为17 × 15 cm。组织病理学证实为软组织肿瘤-平滑肌瘤。结论:宽韧带平滑肌瘤在临床和影像学检查上与卵巢肿瘤相似,两者难以鉴别。由于其不寻常的表现,其临床和放射学特征诊断困难。因此,组织病理学对其诊断起着重要的作用。临床意义:我们提出这个病例,因为它的罕见和诊断困难。
A Rare Case of Broad Ligament Fibroid: A Case Report
Ab s t r Ac t Background: The broad ligament is the commonest extrauterine site for occurrence of leiomyoma. Because of its rarity, it poses both clinical and radiological difficulties in differentiating against an ovarian tumor. Case description: We are presenting a rare case of leiomyoma of broad ligament in a 45-year-old female with complaints of lower abdominal lump, pain, and menstrual abnormality. On clinical examination, there was a 18-week-old firm, nontender, and mobile mass extending to the umbilicus. Ultrasound pelvis showed a large hypoechoic lesion of 17 cm × 11 cm × 10.3 cm with internal vascularity in pelvis predominantly on the left side. MRI pelvis showed similar findings. IVP was normal. Result: Laparotomy showed a huge false left-sided broad ligament leiomyoma measuring 17 × 15 cm. Histopathology confirmed it to be a soft tissue tumor-leiomyoma. Conclusion: Broad ligament leiomyomas mimic ovarian tumors on clinical and radiological examination and may pose difficulties in differentiating both. Its diagnosis is difficult on clinical and radiological features owing to its unusual presentation. Thus histopathology plays an important role in confirming its diagnosis. Clinical significance: We present this case because of its rarity and the diagnostic difficulties it posed.