Eight cases of papillary serous cystadenoma arising in paramesonephric parovarian cysts are presented. None of these benign lesions were diagnosed preoperatively as such and were only detected pathologically. In only one case was the tumor-bearing cyst symptomatic owing to its large size. The etiology, pathogenesis, and evolution of this lesion are briefly discussed.
Download full-text PDF |
Source |
|---|---|
| http://dx.doi.org/10.3109/00016348009155444 | DOI Listing |
Publication Analysis
Top Keywords
Similar Publications
Symptomatic leiomyoma in a patient with a bicornuate uterus: A rare case report.
Int J Surg Case Rep
October 2024
Faculty of Medicine, Kilimanjaro Christian Medical University College, Moshi, Tanzania; Department of Pathology, Kilimanjaro Christian Medical Center, Moshi, Tanzania; Kilimanjaro Clinical Research Institute, Moshi, Tanzania. Electronic address:
Article Synopsis
- * A 30-year-old woman with abdominal swelling was found to have a bicornuate uterus and a large cystic mass that was surgically removed, revealing a fibroid (leiomyoma).
- * Proper evaluation through imaging is crucial for managing conditions involving bicornuate uterus and fibroids, as these cases can pose diagnostic challenges and affect reproductive outcomes.
Management of congenital cervical atresia with vaginal aplasia: A case report and review of the literature.
Int J Surg Case Rep
August 2024
Department of Obstetrics and Gynecology, Oncology and High-Risk Pregnancies, Maternity Hospital Souissi, University Hospital Center IBN SINA, University Mohammed V, Rabat, Morocco.
Introduction: Vaginal agenesis is a rare congenital condition, with an incidence of 1 in 4500 female births.
Case Report: We present a clinical case of vaginal aplasia with cervical atresia in a 31-year-old woman with primary amenorrhea. We aim to report the diagnostic process and provide a comprehensive outline of different possible treatments.
Mayer-Rokitansky-Kuster-Hauser syndrome complicated with giant mucinous cystadenoma and inguinal herniation: case report.
Oxf Med Case Reports
April 2024
Department of Obstetrics and Gynecology, Universitas Padjadjaran, Bandung, West Java, Indonesia.
Introduction: Coexistence of Mayer-Rokitansky-Kuster-Hauster syndrome (MRKH) with other conditions is rare, especially when MRKH was found in a young woman presenting with ovarian malignancy. This case report wishes to highlight MRKH complicated with giant mucinous cystadenoma and bilateral inguinal hernia.
Case Report: A 22-year-old nulligravid woman was admitted with primary amenorrhea and abdominal mass.
Want AI Summaries of new PubMed Abstracts delivered to your In-box?
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!