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1.
J Am Assoc Gynecol Laparosc ; 10(3): 316-9, 2003 Aug.
Article in English | MEDLINE | ID: mdl-14567804

ABSTRACT

STUDY OBJECTIVE: To evaluate whether uterine shrinkage induced by gonadotropin-releasing hormone (GnRH) agonists in women with a large uterus (>14 wks) may facilitate total laparoscopic hysterectomy. DESIGN: Randomized, prospective study (Canadian Task Force classification I). SETTING: University-affiliated hospital. PATIENTS: Sixty-two women with symptomatic uterine myomas (size 16-20 wks). INTERVENTIONS: Total laparoscopic hysterectomy for benign pathology. MEASUREMENTS AND MAIN RESULTS: Before surgery, women were assigned, at a ratio of 1:1 by random selection, to receive injections of triptorelin depot 11.25 mg 3 months before surgery (group A) or no treatment (group B). Uterine volume, mean operating time, uterine weight, drop in hemoglobin, intraoperative complications, conversions to laparotomy, and hospital stay were recorded. Triptorelin decreased uterine volume, calculated by ultrasonography, by 26.5% in group A, whereas the volume remained unchanged in group B. Statistical differences were found between groups concerning uterine weight, operating time, and drop in hemoglobin level. Three patients in group B were converted to laparotomy because of uterine size. CONCLUSION: In women with a large uterus, a 3-month preoperative course of GnRH may facilitate laparoscopic hysterectomy, decreasing uterine size, operating time, and blood loss.


Subject(s)
Antineoplastic Agents, Hormonal/therapeutic use , Hysterectomy , Laparoscopy , Leiomyoma/surgery , Triptorelin Pamoate/therapeutic use , Uterine Neoplasms/surgery , Female , Humans , Middle Aged , Preoperative Care , Prospective Studies , Time Factors , Uterus/drug effects
2.
BJOG ; 110(3): 236-40, 2003 Mar.
Article in English | MEDLINE | ID: mdl-12628260

ABSTRACT

OBJECTIVE: The purpose of the study was to evaluate the post-operative course and follow up of women who had undergone laparoscopic removal of intramural fibroids penetrating the uterine cavity. DESIGN: Retrospective study. SETTING: Center for Reconstructive Pelvic Endosurgery, Italy. POPULATION: Thirty-four women with fibroids penetrating the uterine cavity. METHODS: Laparoscopic myomectomy. MAIN OUTCOME MEASURES: Feasibility and safety of surgical technique, length of operation, blood loss, intra- or post-operative complications, length of hospital stay, resolution of symptoms and future obstetric outcome. RESULTS: The mean operative time was 79 (SD 30) minutes; the mean reduction in haemoglobin was 1.1 +/- 0.9 g/dL. No intra- or post-operative complications were observed. The average post-operative stay in hospital was 54 (SD 22) hours. Nineteen (73%) out of 26 patients who had experienced symptoms prior to surgery reported resolution of these symptoms post-operatively. All patients resumed work within a mean time of 20 (SD 8) days. Among 23 of the 32 patients attempting pregnancy during the follow up period, nine (39%) conceived within one year. Seven pregnancies went to term without complications. CONCLUSIONS: The clinical results of this study suggest that laparoscopic myomectomy for intramural fibroids penetrating the uterine cavity is a safe procedure, providing well known advantages of minimal access surgery.


Subject(s)
Laparoscopy/adverse effects , Leiomyoma/surgery , Postoperative Complications/etiology , Uterine Neoplasms/surgery , Adult , Blood Loss, Surgical , Feasibility Studies , Female , Follow-Up Studies , Humans , Leiomyoma/pathology , Length of Stay , Middle Aged , Retrospective Studies , Treatment Outcome , Uterine Neoplasms/pathology
3.
Fertil Steril ; 76(5): 999-1004, 2001 Nov.
Article in English | MEDLINE | ID: mdl-11704124

ABSTRACT

OBJECTIVE: To evaluate the efficacy of laparoscopic conservative surgery in young women with borderline ovarian tumors who want to preserve their childbearing potential, and to assess whether pregnancy influences the recurrence rate during the follow-up evaluation period. DESIGN: Retrospective study. SETTING: Center for Reconstructive Pelvic Endosurgery, Reproductive Medicine Unit, S. Orsola Hospital, University of Bologna, Italy. PATIENT(S): Nineteen women (mean age 27.4 +/- 4.7) with borderline ovarian tumors who underwent laparoscopy between January 1995 and January 1998. All of the women wanted to preserve their fertility. INTERVENTION(S): A standardized conservative laparoscopic approach and a strict follow-up schedule. MAIN OUTCOME MEASURE(S): A complete preoperative examination. RESULT(S): Follow-up evaluations (mean 42 +/- 19 months) were made available to all patients. Among 19 patients, 10 attempted pregnancy and 6 conceived spontaneously. All six pregnancies went to term and the disease did not affect the gestation or the follow-up period after the pregnancy (24.5 +/- 15.7 months). CONCLUSION(S): Conservative laparoscopic management of borderline ovarian tumors is a potentially safe alternative in young women who want to retain their childbearing potential. Fertility and pregnancy outcome remain excellent in these women. Our preliminary data seem to indicate that the recurrence rate after pregnancy is not influenced by this approach.


Subject(s)
Fertility , Laparoscopy , Neoplasm Recurrence, Local , Ovarian Neoplasms/surgery , Pregnancy Complications, Neoplastic/surgery , Adult , Female , Follow-Up Studies , Humans , Pregnancy , Pregnancy Outcome , Retrospective Studies
4.
Hum Reprod ; 16(6): 1261-3, 2001 Jun.
Article in English | MEDLINE | ID: mdl-11387302

ABSTRACT

The case of recurrent bilateral ovarian fibromas occurring in a 22 year old Italian girl affected by Gorlin syndrome is reported. Ovarian fibromas occur in 75% of female patients with Gorlin syndrome and their recurrence has rarely been reported in the literature. Management is guided by the benign nature of the lesion and consists of surgical removal of the fibroma. Preservation of the normal ovarian tissue is recommended even though there is risk of recurrence of the fibroma.


Subject(s)
Basal Cell Nevus Syndrome/complications , Fibroma/surgery , Ovarian Neoplasms/surgery , Adult , Basal Cell Nevus Syndrome/genetics , Female , Fibroma/etiology , Fibroma/pathology , Frameshift Mutation , Humans , Leiomyoma/etiology , Leiomyoma/pathology , Leiomyoma/surgery , Neoplasm Recurrence, Local , Ovarian Neoplasms/etiology , Ovarian Neoplasms/pathology , Polymerase Chain Reaction , Uterine Neoplasms/etiology , Uterine Neoplasms/pathology , Uterine Neoplasms/surgery
5.
Horm Res ; 56(1-2): 25-31, 2001.
Article in English | MEDLINE | ID: mdl-11815724

ABSTRACT

OBJECTIVE: To evaluate the safety and efficacy of a low dose of flutamide (125 mg/day) in maintaining the clinical results already obtained using a higher dose (250 mg/day), in women suffering from hirsutism. METHOD: Forty-three women suffering from hirsutism of varying origin received 250 mg/day of flutamide as an initial treatment for 12 months and, subsequently, 125 mg/day of flutamide for an additional 12 months as a maintenance treatment. Hirsutism was evaluated by the Ferriman-Gallwey score, and hair diameter and hair growth rate were determined by a special image analysis processor. Biochemical, clinical and hormonal parameters were evaluated in basal conditions and every 2-6 months. RESULTS: The significant decrease in the hirsutism score, hair diameter and hair growth rate during the initial treatment period was confirmed at the end of the maintenance treatment period. Androgen levels decreased up to the end of the initial treatment period and partially decreased during the maintenance treatment. During the initial treatment period, 4 subjects showed an increase of aspartate aminotransferase and alanine aminotransferase and dropped out. During the maintenance treatment period, no side effects or complications were observed. CONCLUSION: Satisfactory management of hirsutism with flutamide seems to be represented by an initial treatment period using 250 mg/day to achieve satisfactory results, followed by a long maintenance treatment period using 125 mg/day.


Subject(s)
Androgen Antagonists/administration & dosage , Flutamide/administration & dosage , Hirsutism/drug therapy , Adult , Alanine Transaminase/blood , Androgen Antagonists/adverse effects , Androgen Antagonists/therapeutic use , Aspartate Aminotransferases/blood , Dose-Response Relationship, Drug , Drug Administration Schedule , Female , Flutamide/adverse effects , Flutamide/therapeutic use , Hirsutism/blood , Hormones/blood , Humans , Single-Blind Method , Treatment Outcome
6.
J Clin Endocrinol Metab ; 84(4): 1304-10, 1999 Apr.
Article in English | MEDLINE | ID: mdl-10199771

ABSTRACT

Sixty-six hirsute women were randomized and treated with 1) flutamide (n = 15), 250 mg/day; 2) finasteride (n = 15), 5 mg/day; 3) ketoconazole (n = 16), 300 mg/day; and 4) ethinyl estradiol (EE)-cyproterone acetate (CPA; n = 20), 0.01 mg EE/day for the first week, 0.02 mg EE/day for the second week, and 0.01 mg EE/day for the third week, followed by a pause of 7 days, then 12.5 mg CPA/day added during the first 10 days of every month for 12 months. Hirsutism was evaluated by the Ferriman-Gallwey score, and hair diameter and hair growth rate were determined by a special image analysis processor in basal conditions and after 90, 180, 270, and 360 days of treatment. All treatments produced a significant decrease in the hirsutism score, hair diameter, and daily hair growth rate: flutamide, -55 +/- 13%, -21 +/- 14%, and -37 +/- 18%; finasteride, -44 +/- 13%, -16 +/- 12%, and -27 +/- 14%; ketoconazole, -53 +/- 18%, -14 +/- 12%, and -30 +/- 21%; and EE-CPA, -60 +/- 18%, -20 +/- 11%, and -28 +/- 21%. Some differences existed among treatments with regard to effectiveness; EE-CPA and flutamide seem to be the most efficacious in improving hirsutism. For the hirsutism score, a greater decrease was seen with EE-CPA (-60 +/- 18%) than with finasteride (-44 +/- 13%; P < 0.01) and a greater decrease was seen with flutamide (-58 +/- 18%) than with finasteride (-44 +/- 13%; P < 0.05). Flutamide is the fastest in decreasing hair diameter; EE-CPA is the fastest in slowing down hair growth, even though at the end of the treatment there was a significant difference between flutamide and finasteride only (-41 +/- 18% vs. -27 +/- 14%; P < 0.05). Flutamide, ketoconazole, and EE-CPA induced a significant decrease in total and free testosterone, 5alpha-dihydrotestosterone, dehydroepiandrosterone, dehydroepiandrosterone sulfate, and androstenedione plasma levels. During the EE-CPA treatment, gonadotropins were suppressed, and the sex hormone-binding globulin level increased. Finasteride induced a decrease in dehydroepiandrosterone sulfate and 5alpha-dihydrotestosterone and an increase in testosterone levels. Very few side-effects were observed during treatment with low doses of flutamide, EE-CPA, and particularly finasteride. Flutamide induced a decrease whereas EE-CPA induced an increase in triglycerides and cholesterol, showing higher values within the normal range. Ketoconazole induced several side-effects and complications, and several people dropped out of the study. Despite different modalities of action and significantly different effects on androgen levels, low doses of flutamide, finasteride, and EE-CPA constitute very satisfactory alternative therapeutic regimens in the treatment of hirsutism.


Subject(s)
Cyproterone Acetate/administration & dosage , Ethinyl Estradiol/administration & dosage , Finasteride/therapeutic use , Flutamide/therapeutic use , Hirsutism/drug therapy , Ketoconazole/therapeutic use , Adult , Cyproterone Acetate/adverse effects , Ethinyl Estradiol/adverse effects , Female , Finasteride/adverse effects , Flutamide/adverse effects , Hormones/blood , Humans , Ketoconazole/adverse effects , Prospective Studies
7.
Eur J Contracept Reprod Health Care ; 3(1): 29-33, 1998 Mar.
Article in English | MEDLINE | ID: mdl-9678070

ABSTRACT

OBJECTIVE: To compare the effectiveness of two very low-dose ethinylestradiol and cyproterone acetate regimens in the treatment of hirsutism. PATIENTS: Eighteen hirsute women were randomized into two different regimens of cyproterone acetate and ethinylestradiol in a reverse sequential pattern: group 1 (0.28 mg ethinylestradiol monthly), group 2 (0.32 mg ethinylestradiol monthly). Both groups received 12.5 mg/day cyproterone acetate for the first 10 days of treatment each month. MAIN OUTCOME MEASURES: Hirsutism scores were measured according to the Ferriman and Gallwey scoring system and side-effects and complications were recorded during the 6 months of therapy. Ovulation was monitored by radioimmunoassay of estradiol, follicle stimulating hormone (FSH), luteinizing hormone (LH) and progesterone levels. The pituitary response was studied using a gonadotropin releasing hormone test. RESULTS: Hirsutism scores decreased significantly in both groups at the end of the 6 months (-30%). All patients were anovulatory, as documented by the reduction of the LH, FSH, estradiol and progesterone levels. Pretreatment basal LH and FSH levels were higher than LH and FSH levels during the treatment. Side-effects were observed only occasionally with some differences between the two therapeutic regiments. CONCLUSION: Both treatments greatly improve hirsutism, reduce clinical problems and side-effects, guarantee both anovulation and contraceptive effectiveness and afford an optimal control of the menstrual cycle.


Subject(s)
Contraceptives, Oral, Sequential/therapeutic use , Cyproterone Acetate/therapeutic use , Estradiol Congeners/therapeutic use , Ethinyl Estradiol/therapeutic use , Hirsutism/drug therapy , Progesterone Congeners/therapeutic use , Adult , Estradiol/blood , Female , Follicle Stimulating Hormone/blood , Hirsutism/metabolism , Humans , Luteinizing Hormone/blood , Progesterone/blood , Severity of Illness Index
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