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1.
Eur J Gynaecol Oncol ; 38(1): 59-64, 2017.
Article in English | MEDLINE | ID: mdl-29767866

ABSTRACT

Ovarian cancer forms 4% of all cancers and approximately 23% of all gynecological cancers in women and is responsible for the 47% of deaths related to cancers of the genital tract of women. Tumor markers are the biochemical substances which can be detected in the presence of tumors. Generally they are either the products of tumoral tissues or secreted from the normal cells which are in the inter- action with tumoral ones. The present authors attempted to determine the efficacy of the tumor marker CA- 125 and HE4 to differentiate the malign cases from the benign adnexal masses. A total of 76 patients with the appropriate criteria were included in the study. They were divided into three groups; healthy control group (n=3 1), ones with benign masses (n=23), and ones with malign ovarian masses (n=22). In the study, when the cut-off values were accepted as 55I U/ml for CA-125 and 150 pM for HE4 in differentiation of benign and malign groups, the sensitivity was found as 59.09%, specificity 91.3%, PPV 86.67% and NPV 70% LR = +6.8. This combination gives one false positive result to every five positive cases which were detected as high. With the combination of CA-125 and HE4, the value of sensitivity was found decreased as expected, although the value of the specificity increased.


Subject(s)
CA-125 Antigen/blood , Ovarian Neoplasms/blood , Ovarian Neoplasms/diagnosis , Proteins/metabolism , Adult , Case-Control Studies , Female , Humans , Middle Aged , Predictive Value of Tests , ROC Curve , WAP Four-Disulfide Core Domain Protein 2
2.
BJOG ; 122(1): 80-91, 2015 Jan.
Article in English | MEDLINE | ID: mdl-25209926

ABSTRACT

OBJECTIVE: To evaluate the effectiveness of 200 mg of daily vaginal natural progesterone to prevent preterm birth in women with preterm labour. DESIGN: Multicentre, randomised, double-blind, placebo-controlled trial. SETTING: Twenty-nine centres in Switzerland and Argentina. POPULATION: A total of 385 women with preterm labour (24(0/7) to 33(6/7) weeks of gestation) treated with acute tocolysis. METHODS: Participants were randomly allocated to either 200 mg daily of self-administered vaginal progesterone or placebo within 48 hours of starting acute tocolysis. MAIN OUTCOME MEASURES: Primary outcome was delivery before 37 weeks of gestation. Secondary outcomes were delivery before 32 and 34 weeks, adverse effects, duration of tocolysis, re-admissions for preterm labour, length of hospital stay, and neonatal morbidity and mortality. The study was ended prematurely based on results of the intermediate analysis. RESULTS: Preterm birth occurred in 42.5% of women in the progesterone group versus 35.5% in the placebo group (relative risk [RR] 1.2; 95% confidence interval [95% CI] 0.93-1.5). Delivery at <32 and <34 weeks did not differ between the two groups (12.9 versus 9.7%; [RR 1.3; 95% CI 0.7-2.5] and 19.7 versus 12.9% [RR 1.5; 95% CI 0.9-2.4], respectively). The duration of tocolysis, hospitalisation, and recurrence of preterm labour were comparable between groups. Neonatal morbidity occurred in 44 (22.8%) cases on progesterone versus 35 (18.8%) cases on placebo (RR: 1.2; 95% CI 0.82-1.8), whereas there were 4 (2%) neonatal deaths in each study group. CONCLUSION: There is no evidence that the daily administration of 200 mg vaginal progesterone decreases preterm birth or improves neonatal outcome in women with preterm labour.


Subject(s)
Birth Weight , Obstetric Labor, Premature/drug therapy , Premature Birth/prevention & control , Progesterone/therapeutic use , Progestins/therapeutic use , Administration, Intravaginal , Adult , Apgar Score , Double-Blind Method , Female , Humans , Indomethacin/therapeutic use , Infant , Infant Mortality , Infant, Newborn , Intensive Care Units, Neonatal/statistics & numerical data , Pregnancy , Pregnancy Trimester, Second , Pregnancy Trimester, Third , Receptors, Oxytocin/antagonists & inhibitors , Tocolytic Agents/therapeutic use , Young Adult
3.
J Int Med Res ; 36(1): 88-95, 2008.
Article in English | MEDLINE | ID: mdl-18230272

ABSTRACT

This study investigated whether microvessel density (MVD) and mast cell infiltration are related to prognosis in non-small cell lung carcinoma (NSCLC), and examined the possible role of mast cells in NSCLC angiogenesis. MVD and mast cell infiltration were analysed retrospectively in tumour specimens from 50 patients with primary NSCLC. Immunohistochemistry with monoclonal antibody anti-CD34 was used to delineate the microvessels and routine Giemsa blue staining was used to assess the number of mast cells. Significant correlations were found between MVD and mast cell infiltration and between MVD and both lymph node metastasis and tumour, node, metastases (TNM) stage. No significant correlations were found with respect to survival for MVD or mast cell infiltration. Multivariate analysis showed that TNM stage and tumour size were independent predictors of survival, suggesting that the TNM staging system remains the most important tool for the estimation of prognosis in NSCLC patients.


Subject(s)
Carcinoma, Non-Small-Cell Lung/blood supply , Lung Neoplasms/blood supply , Mast Cells/pathology , Neovascularization, Pathologic/diagnosis , Adult , Aged , Antigens, CD34/analysis , Carcinoma, Non-Small-Cell Lung/mortality , Female , Humans , Immunoenzyme Techniques , Lung Neoplasms/mortality , Male , Middle Aged , Prognosis , Survival Rate
4.
Eur J Gynaecol Oncol ; 26(3): 342-4, 2005.
Article in English | MEDLINE | ID: mdl-15991543

ABSTRACT

Malignant neoplasms of the fallopian tube are the rarest of the gynecologic cancers. The frequency of histologic subtypes has been difficult to ascertain from the literature because most authors have not classified these tumors according to their cell types. Papillary serous adenocarcinoma appears to be the most common histologic type. On the contrary, mixed cell types of fallopian tube carcinoma have rarely been reported in the literature. A case of mixed serous and endometrioid carcinoma of the fallopian tube is presented and the related literature is reviewed.


Subject(s)
Antineoplastic Combined Chemotherapy Protocols/therapeutic use , Carcinoma, Endometrioid/pathology , Cystadenocarcinoma, Serous/pathology , Fallopian Tube Neoplasms/pathology , Mixed Tumor, Malignant/pathology , Adult , Carboplatin/administration & dosage , Carcinoma, Endometrioid/therapy , Cyclophosphamide/administration & dosage , Cystadenocarcinoma, Serous/therapy , Fallopian Tube Neoplasms/therapy , Female , Gynecologic Surgical Procedures , Humans , Mixed Tumor, Malignant/therapy , Neoplasm Staging , Paclitaxel/administration & dosage , Treatment Outcome
5.
Eur J Gynaecol Oncol ; 25(4): 528-9, 2004.
Article in English | MEDLINE | ID: mdl-15285324

ABSTRACT

Sclerosing stromal tumors of the ovary are distinct, but rare benign neoplasms. These tumors appear solid and are very vascular giving the impression of malignant tumors. They occur mostly in young women. Morphologically they have distinct characteristics which differentiate them from other stromal tumors. Benign ovarian tumors associated with Meigs' syndrome are rare. In this article a case of ovarian sclerosing stromal tumor associated with Meigs' syndrome in a 17-year-old women is described and the differential diagnosis is also discussed.


Subject(s)
Meigs Syndrome/diagnosis , Sex Cord-Gonadal Stromal Tumors/pathology , Sex Cord-Gonadal Stromal Tumors/surgery , Adolescent , Biopsy, Needle , Female , Follow-Up Studies , Humans , Immunohistochemistry , Meigs Syndrome/complications , Meigs Syndrome/surgery , Neoplasm Staging , Ovarian Neoplasms/complications , Ovarian Neoplasms/pathology , Ovarian Neoplasms/surgery , Ovariectomy/methods , Risk Assessment , Sex Cord-Gonadal Stromal Tumors/complications , Treatment Outcome
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