A Case Report of Pseudomyxoma Peritonei Arising From Primary Mucinous Ovarian Neoplasms
- PMID: 36277572
- PMCID: PMC9579829
- DOI: 10.7759/cureus.29309
A Case Report of Pseudomyxoma Peritonei Arising From Primary Mucinous Ovarian Neoplasms
Abstract
Pseudomyxoma peritonei (PMP) is a rare manifestation of primary mucinous neoplasms. We report two rare cases of PMP originating from mucinous primary ovarian neoplasms. The case series discusses the cases of female patients aged 86 and 52 years who presented with worsening dyspepsia, abdominal distension, pelvic pain, and altered bowel habits. Both of the patients underwent evaluation comprising cancer antigen-125 (CA-125) levels, ultrasound (US) examination of the abdomen and the pelvis, tumor markers, cytological evaluation, and contrast-enhanced computed tomography (CECT) of the pelvis and abdomen. Patients were diagnosed to have pseudomyxoma peritonei arising from mucinous ovarian tumors. Patients were referred to the surgical department and were successfully managed with repeated removal of mucinous material. The present case report highlights the significant radio-pathologic characteristics of PMP, which originated from mucinous ovarian tumors.
Keywords: abdominal radiology; academic radiology; appendix; cystic mass; mucinous neoplasms; ovary; pseudomyxoma peritonei.
Copyright © 2022, Joseph et al.
Conflict of interest statement
The authors have declared that no competing interests exist.
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References
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- A consensus for classification and pathologic reporting of pseudomyxoma peritonei and associated appendiceal neoplasia: the results of the peritoneal surface oncology group international (PSOGI) modified Delphi process. Carr NJ, Cecil TD, Mohamed F, et al. Am J Surg Pathol. 2016;40:14–26. - PubMed
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- Pseudomyxoma peritonei: natural history and treatment. Mittal R, Chandramohan A, Moran B. Int J Hyperthermia. 2017;33:511–519. - PubMed
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