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Pseudomyxoma peritonei - case report

  • O. Nikolic1,*,
  • S. Djurdjevic2
  • S. Stojanovic1
  • M. Basta Nikolic1
  • M. Mocko Kacanski3
  • S. Secen4

1Department of Radiology, Clinical Center of Vojvodina, Novi Sad, Serbia

2Department of Gynecology and Obstetrics, Clinical Center of Vojvodina, Novi Sad, Serbia

3Department of Histhopathology, Medical Faculty, Univeristy of Novi Sad, Novi Sad 21000, Serbia

4Department of Abdominal Surgery, Clinical Center of Vojvodina, Novi Sad, Serbia

DOI: 10.12892/ejgo201202227 Vol.33,Issue 2,March 2012 pp.227-229

Published: 10 March 2012

*Corresponding Author(s): O. Nikolic E-mail: nikolic.olivera@gmail.com

Abstract

The syndrome pseudomyxoma peritonei is rare, present in only 2/10,000 laparotomies. We report the case of a 58-year-old woman with a primary tumor of the appendix, and secondary involvement of other structures and organs of the abdominal cavity. In our case, we performed maximal surgical reduction of the tumor, with remaining implants on diaphragmatic domes and liver, as we did not have technical conditions to safely perform prolonged surgery which would have included a surgical procedure on the liver and administration of intraoperative chemotherapy. The patient underwent six series of parenteral chemotherapy, but refused the second-look surgery. Even though our patient did not receive intraperitoneal chemotherapy, maximal surgical tumor reduction, and refused second-look surgery, she is still alive and without any major complaints two years after the surgery.

Keywords

Pseudomyxoma peritonei; Appendix; Ovary; Diagnosis; Treatment

Cite and Share

O. Nikolic,S. Djurdjevic,S. Stojanovic,M. Basta Nikolic,M. Mocko Kacanski,S. Secen. Pseudomyxoma peritonei - case report. European Journal of Gynaecological Oncology. 2012. 33(2);227-229.

References

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