A Clinicopathologic Analysis of Pseudomyxoma Peritonei Originated from Mucinous Ovarian Tumors.
- Author:
Ji Hyun PARK
;
Young Ho YANG
;
Jae Ho HAN
- Publication Type:Original Article
- Keywords:
Pseudomyxoma peritonei;
Ovarian mucinous tumors;
Borderline malignancy;
Survival
- MeSH:
Adenoma;
Chemotherapy, Adjuvant;
Diagnosis;
Humans;
Mucins*;
Natural History;
Pseudomyxoma Peritonei*;
Recurrence;
Retrospective Studies
- From:Korean Journal of Obstetrics and Gynecology
1999;42(8):1808-1814
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
OBJECTIVE: The aims of this study were to analyze the natural history of patients with pseudomyxoma peritonei originated from mucinous ovarian tumor, evaluate clinical and pathologic variables, and review our experience with available therapeutic modalities. METHODS: Six patients were treated for pseudomyxoma peritonei originating from mucinous ovarian tumor at Severance Hospital between 1990 and 1998. The data were collected retrospectively and all charts were reviewed RESULTS: The mean age at diagnosis was 51 years, and most common symptoms were abdominal distension. Pseudomyxoma peritonei was found in association with five mucinous ovarian tumors of borderline malignancy, and one ovarian mucinous adenoma. All patients underwent surgical staging and cytoreduction, three patients received postoperative adjuvant chemotherapy and, of these, two developed recurrence. With respect to survival, all patients were alive, four were alive and free of disease, two were alive with disease at the end point of study. CONCLUSION: Pseudomyxoma peritonei is commonly associated with borderline mucinous ovarian tumors, and is a frequently relapsing and protracted disease. But aggressive and repeated debulking surgery is recommended for long survival.
