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1.
Tumori ; 92(6): 491-5, 2006.
Article in English | MEDLINE | ID: mdl-17260489

ABSTRACT

AIMS AND BACKGROUND: The aim of this study was to evaluate patients with metastatic ovarian tumors from extragenital primary sites. METHODS: The medical records of 75 patients were reviewed retrospectively for age at diagnosis, presenting symptoms, preoperative tumor marker levels, preoperative diagnostic workup, operative technique, intraoperative evaluation, frozen-section and pathology results, laterality of metastasis, and primary tumor site. The specific impact of metastasis from colorectal and gastric primary sites on laterality, gross features and dimensions of ovarian mass, volume of ascites and tumor marker levels was investigated. RESULTS: Primary sites were stomach (37.3%), colorectal region (28%), lymphoma (12%), breast (6.7%), biliary system (2.7%), appendix (1.3%) and small intestine (1.3%). It was not possible to identify the primary tumor site in 8 (10.7%) patients. Bilateral metastasis was found in 86.4% patients; 42.7% of the metastatic ovarian tumors were Krukenberg tumors; 50.7% of the ovarian masses were solid. Frozen section was confirmed by postoperative pathological results in 98% of the patients. The mean preoperative serum levels of tumor markers were 298.7 U/mL, 178 U/mL and 113.3 U/mL for CA 125, CA 19-9 and CA 15-3, respectively. CA 125 levels were above 35 U/mL in 81.3% of the patients. The presence of ascites was more frequent in ovarian tumors originating from colorectal and gastric primaries. CONCLUSIONS: Surgery is essential for the diagnosis of the primary tumor and necessary for relief of symptoms. The identification of the primary site is required to plan adequate treatment.


Subject(s)
Biomarkers, Tumor/blood , Breast Neoplasms/diagnosis , Digestive System Neoplasms/diagnosis , Lymphoma/diagnosis , Ovarian Neoplasms/secondary , Adult , Aged , Ascites/etiology , Breast Neoplasms/pathology , Breast Neoplasms/surgery , CA-125 Antigen/blood , CA-19-9 Antigen/blood , Carcinoembryonic Antigen/blood , Digestive System Neoplasms/pathology , Digestive System Neoplasms/surgery , Female , Frozen Sections , Humans , Lymphoma/pathology , Lymphoma/surgery , Middle Aged , Neoplasm Staging , Ovarian Neoplasms/blood , Ovarian Neoplasms/complications , Ovarian Neoplasms/surgery , Retrospective Studies , alpha-Fetoproteins/metabolism
2.
Am J Obstet Gynecol ; 187(4): 1038-45, 2002 Oct.
Article in English | MEDLINE | ID: mdl-12389002

ABSTRACT

OBJECTIVE: The purpose of this study was to compare misoprostol 600 microg intrarectally with conventional oxytocics in the treatment of third stage of labor. STUDY DESIGN: In a controlled trial, 1606 women were randomly grouped to receive (1) oxytocin 10 IU plus rectal misoprostol, (2) rectal misoprostol, (3) oxytocin 10 IU, and (4) oxytocin 10 IU plus methylergometrine. The main outcome measures were the incidence of postpartum hemorrhage and a drop in hemoglobin concentration from before delivery to 24 hours after delivery. RESULTS: The incidence of postpartum hemorrhage was 9.8% in the group that received only rectal misoprostol therapy compared with 3.5% in the group that received oxytocin and methylergometrine therapy (P =.001). There were no significant differences among the 4 groups with regard to a drop in hemoglobin concentrations. Significantly more women needed additional oxytocin in the group that received only rectal misoprostol therapy, when compared with the group that received oxytocin and methylergometrine therapy (8.3% vs 2.2%; P <.001). The primary outcome measures were similar in the group that received only rectal misoprostol therapy and the group that received only oxytocin therapy. CONCLUSION: Rectal misoprostol is significantly less effective than oxytocin plus methylergometrine for the prevention of postpartum hemorrhage.


Subject(s)
Labor Stage, Third/drug effects , Misoprostol/administration & dosage , Oxytocics/administration & dosage , Postpartum Hemorrhage/prevention & control , Administration, Rectal , Adult , Drug Therapy, Combination , Female , Fever/chemically induced , Humans , Methylergonovine/adverse effects , Methylergonovine/therapeutic use , Misoprostol/adverse effects , Misoprostol/therapeutic use , Oxytocics/adverse effects , Oxytocics/therapeutic use , Oxytocin/adverse effects , Oxytocin/therapeutic use , Pregnancy
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