Abstract
Aim: Pseudomyxoma peritonei (PMP) is a rare disease characterized by the abundance of mucus in the abdomen without extra-peritoneal growth. Methods: Our patients with PMP have been treated with cytoreduction and hyperthermic intraperitoneal chemotherapy since 1996. The clinical and histopathological features of PMP and the relation of these features with disease-free interval and survival were assessed. Results: Sixty-two patients with PMP (24 M/38 F) were studied. Adenomatous mucosal changes were present in 31 patients. In females, the ovaries were normal in 5 patients and pseudomyxoma ovarii was present in 20 patients. Patients with minimal atypia and with 1% focal proliferation or less (n = 38) had a better survival (p = 0.0008) than those with more focal proliferation (n = 14). Conclusion: In most patients with PMP the appendix is affected; in females the ovaries are usually also involved. Focal proliferation appears to be a prognostic factor.
Original language | English |
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Pages (from-to) | 682-688 |
Journal | European Journal of Surgical Oncology |
Volume | 29 |
Issue number | 8 |
DOIs | |
Publication status | Published - 2003 Oct |
Externally published | Yes |
Subject classification (UKÄ)
- Cancer and Oncology
Free keywords
- Disseminated peritoneal adenomucinosis
- HIPEC
- Pathology
- Peritoneal mucinous carcinomatosis with intermediate or discordant features
- Pseudomyxoma peritonei