Volume 10, Issue 3 (2025)                   SJMR 2025, 10(3): 125-130 | Back to browse issues page


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Nateghi M R, Alijani L, Sanaye Naderi M, Mohammadian H. Primary Retroperitoneal Mucinous Cystadenocarcinoma in Pregnancy (PRMC): A Very Rare Case Report, Diagnostic and Therapeutic Challenges. SJMR 2025; 10 (3) : 3
URL: http://saremjrm.com/article-1-374-en.html
1- Sarem Gynecology, Obstetrics and Infertility Research Center, Sarem Women’s Hospital, Iran University of Medical Sciences, Tehran, Iran. & Sarem Cell Research Center (SCRC), Sarem Women’s Hospital, Tehran, Iran.
2- Sarem Gynecology, Obstetrics and Infertility Research Center, Sarem Women’s Hospital, Iran University of Medical Sciences, Tehran, Iran.
Abstract:   (15 Views)
Introduction: Primary retroperitoneal mucinous cystadenocarcinoma (PRMC) is an exceedingly rare tumor, and its diagnosis during pregnancy poses significant challenges. The scarcity of clinical evidence and the complexity of differential diagnoses further complicate management. The aim of this report was to present and analyze a rare case of PRMC in pregnancy and to review the associated diagnostic and therapeutic considerations.
Case Presentation: A 46-year-old multiparous woman with a history of multiple pregnancies and repeated IVF cycles (the most recent with donor oocytes) was found to have a right adnexal cyst measuring 8 cm on routine ultrasound at 28 weeks of gestation. Tumor markers were within normal ranges, and the cyst showed no significant growth until 33 weeks. Based on a multidisciplinary decision and to ensure fetal lung maturity, the patient received betamethasone and magnesium sulfate. At 34 weeks, a cesarean section was performed via a midline incision, resulting in the delivery of a healthy infant with Apgar scores of 9 and 8. Intraoperatively, adnexa appeared normal; however, a retroperitoneal mass measuring approximately 9×8 cm was unexpectedly discovered and completely excised. Final histopathology confirmed PRMC. Postoperative follow-up, including colonoscopy, upper endoscopy, abdominopelvic CT scan, ultrasonography, and mammography, revealed no pathological findings.
Conclusion: This case demonstrates that PRMC may present during pregnancy with minimal clinical manifestations and normal tumor markers. Timely diagnosis, multidisciplinary decision-making, and appropriate timing of surgical intervention are critical for successful management. Comprehensive postoperative follow-up is essential to exclude secondary origins and to monitor for possible recurrence.
Article number: 3
Full-Text [PDF 442 kb]   (4 Downloads)    
Article Type: Case Report | Subject: Pregnancy Care
Received: 2025/09/22 | Accepted: 2025/09/25 | Published: 2025/09/27

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