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Reproductive Biomedicine
Thu, Nov 21, 2024
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Volume 22, Issue 5 (May 2024)
IJRM 2024, 22(5): 405-410 |
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Hajisafari Tafti M, Zare Garizi S, Mazidi F. Tubal ectopic molar pregnancy: A case report. IJRM 2024; 22 (5) :405-410
URL: http://ijrm.ir/article-1-3336-en.html
URL: http://ijrm.ir/article-1-3336-en.html
1- Department of Obstetrics and Gynecology, School of Medicine, Shahid Sadoughi University of Medical Sciences, Yazd, Iran. & Research and Clinical Center for Infertility, Yazd Reproductive Sciences Institute, Shahid Sadoughi University of Medical Sciences, Yazd, Iran.
2- Student Research Committee, Shahid Sadoughi University of Medical Sciences, Yazd, Iran.
3- Department of Obstetrics and Gynecology, School of Medicine, Shahid Sadoughi University of Medical Sciences, Yazd, Iran. ,mazidifateme826@gmail.com
2- Student Research Committee, Shahid Sadoughi University of Medical Sciences, Yazd, Iran.
3- Department of Obstetrics and Gynecology, School of Medicine, Shahid Sadoughi University of Medical Sciences, Yazd, Iran. ,
Abstract: (288 Views)
Background: Ectopic molar pregnancy (EMP) is a rare form of gestational trophoblastic disease that occurs when a hydatidiform mole implants outside the uterus.
Case Presentation: We describe a 35-yr-old woman with mild abdominal pain, delayed menstruation for 2 months, and high beta-human chorionic gonadotropin levels. Sonography revealed a heterogeneous hyperechoic mass in the left adnexa and fluid in the endometrial cavity, suggestive of a tubal EMP. She underwent endometrial curettage and left salpingectomy. Pathology confirmed the diagnosis of invasive hydatidiform mole/left tubal EMP. The case recovered well and had no complications.
Conclusion: This case highlights the need for early diagnosis and multidisciplinary treatment of EMP to avoid serious consequences from persistent trophoblastic tumors.
Case Presentation: We describe a 35-yr-old woman with mild abdominal pain, delayed menstruation for 2 months, and high beta-human chorionic gonadotropin levels. Sonography revealed a heterogeneous hyperechoic mass in the left adnexa and fluid in the endometrial cavity, suggestive of a tubal EMP. She underwent endometrial curettage and left salpingectomy. Pathology confirmed the diagnosis of invasive hydatidiform mole/left tubal EMP. The case recovered well and had no complications.
Conclusion: This case highlights the need for early diagnosis and multidisciplinary treatment of EMP to avoid serious consequences from persistent trophoblastic tumors.
Type of Study: Case Report |
Subject:
Reproductive Oncology
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