Atypical polypoid adenomyoma: insights into recurrence, malignant transformation and management: a case report

Authors

  • Kitty E. Mammen Department of Obstetrics and Gynecology, Travancore Medical College Hospital, Kollam, Kerala, India
  • Asiya Sheeba Department of Obstetrics and Gynecology, Travancore Medical College Hospital, Kollam, Kerala, India
  • Swapna S. Pillai Department of Obstetrics and Gynecology, Travancore Medical College Hospital, Kollam, Kerala, India
  • Indira Praseeda Department of Pathology, Travancore Medical College Hospital, Kollam, Kerala, India
  • Chandni Thomas Department of Pathology, Travancore Medical College Hospital, Kollam, Kerala, India

DOI:

https://doi.org/10.18203/2320-1770.ijrcog20250212

Keywords:

Atypical polypoid adenomyoma, Recurrent endometrial polyp, Malignancy

Abstract

Atypical polypoid adenomyoma (APAM) is a rare, benign mixed epithelial-mesenchymal tumor of the uterus. It is characterized by its polypoid growth pattern and atypical histological features. This study aims to consolidate current knowledge regarding its clinical presentation, diagnostic criteria, treatment options, and potential for malignancy. There is a significant rate of recurrence associated with this tumor. It consists of unusual endometrial glands interspersed with bundles of smooth muscle fibers. It is frequently diagnosed in young women and may coexist with or progress to atypical endometrial hyperplasia or endometrioid endometrial carcinoma. We report a case of a 35-year-old woman affected by APAM treated with hysteroscopic resection. Given the risk of recurrence and progression, APAM might be treated via hysterectomy in patients with no desire for pregnancy.

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References

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Published

2025-01-29

How to Cite

Mammen, K. E., Sheeba, A., Pillai, S. S., Praseeda, I., & Thomas, C. (2025). Atypical polypoid adenomyoma: insights into recurrence, malignant transformation and management: a case report. International Journal of Reproduction, Contraception, Obstetrics and Gynecology, 14(2), 651–655. https://doi.org/10.18203/2320-1770.ijrcog20250212

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Section

Case Reports