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1.
J Obstet Gynaecol Res ; 46(2): 328-336, 2020 Feb.
Article in English | MEDLINE | ID: mdl-31958879

ABSTRACT

AIM: Although the procedure of abdominal trachelectomy has been remarkably improved, preventing subsequent cervical stenosis remains challenging. In this study, we analyzed the clinicopathological risk factors for cervical stenosis to explore the appropriate surgical procedures for the prevention of cervical stenosis following trachelectomy. METHODS: Thirty-two patients who underwent abdominal extended and radical trachelectomy were assessed retrospectively (median follow-up period = 33 months). To evaluate the risk factors, the clinicopathological factors were analyzed by univariate and multivariate analyses. The reconstructed uterine length (UtL), that is, the length between the vaginal end of the neo-cervix and the uterine fundus, was measured by transvaginal ultrasound after surgery. The cut-off value for the UtL was assessed by a receiver operating characteristic (ROC) curve analysis. RESULTS: Cervical stenosis of any grade was observed in 12 patients (grade 1 = 9, grade 3b = 3). Among the various clinicopathological factors, the UtL and cervical length (CL) were significantly related to cervical stenosis following trachelectomy. The multivariate analysis revealed that the UtL, but not CL, is an independent risk factor for stenosis. The ROC curve analysis revealed that stenosis was significantly more likely to occur in patients with a UtL shorter than 53 mm (area under the ROC curve = 0.902). UtL in the patients who became pregnant was longer than that in the patients who did not. No evidence of recurrent cancer was observed during the follow-up period. CONCLUSION: Our proposed method may provide a functional reconstructed uterus with preserving fertility by remaining UtL more than 53 mm.


Subject(s)
Postoperative Complications/prevention & control , Trachelectomy/adverse effects , Uterine Cervical Neoplasms/surgery , Adult , Constriction, Pathologic/etiology , Female , Humans , Incidence , Japan/epidemiology , Organ Sparing Treatments , Postoperative Complications/epidemiology , Postoperative Complications/etiology , Pregnancy , Pregnancy Rate , Trachelectomy/methods
2.
Gynecol Obstet Invest ; 83(6): 600-607, 2018.
Article in English | MEDLINE | ID: mdl-29982252

ABSTRACT

BACKGROUND/AIM: We demonstrated that AT1 and AT2 are expressed and both pathways balance the renin-angiotensin system in endometriosis. MAS1, a specific receptor of angiotensin (1-7), opposes AT1 pathway-associated tissue remodelling. It is not known whether MAS1 has an effect on the pathogenesis of endometriosis or not. MATERIALS AND METHODS: Ovarian endometriotic tissues (endo-Ov) and eutopic endometrial tissues (endo-Em) were obtained from 29 patients with endometrial cysts. Normal endometrial tissues (cont-Em) were obtained from patients without endometriosis. Immunohistochemical staining was performed for MAS1, AT1 and AT2 in the endometriosis-associated tissues. The mRNA levels of these receptors were examined by quantitative reverse transcription PCR. RESULTS: MAS1 was immune-positive at the apical side of the glandular epithelium in the endometriotic lesions. The MAS1 mRNA levels in endo-Ov were increased significantly, irrespective of the menstrual cycle phase. The MAS1 mRNA levels were significantly higher in the proliferative-tissues of the endometriosis patients than in those of the controls. The ratio of the MAS1 to the AT1 mRNA in the proliferative tissues was increased predominantly in the endometriosis patients compared with that in the controls. CONCLUSION: High MAS1 expression in the endometrium might promote the initiation of endometriosis via migration of proliferative tissue.


Subject(s)
Endometriosis/metabolism , Endometrium/metabolism , Proto-Oncogene Proteins/metabolism , Receptor, Angiotensin, Type 2/metabolism , Receptors, G-Protein-Coupled/metabolism , Adult , Endometriosis/pathology , Endometrium/pathology , Female , Humans , Immunohistochemistry , Membrane Transport Proteins/metabolism , Middle Aged , Ovary/metabolism , Ovary/pathology , Proto-Oncogene Mas , Real-Time Polymerase Chain Reaction , Young Adult
3.
BMC Pregnancy Childbirth ; 17(1): 312, 2017 Sep 20.
Article in English | MEDLINE | ID: mdl-28931393

ABSTRACT

BACKGROUND: The increase in serum estradiol (E2) concentrations during the follicular phase becomes the index of oocyte maturation in vivo. When ovarian stimulation is performed to hypogonadotropic hypogonadism (HH) patients with only follicle stimulating hormone (FSH), proper increase in serum E2 concentrations is not observed. Even if oocytes are obtained, which usually have low fertilization rate. In this report, we would like to present an unique case, in which under low E2 concentrations and without luteinizing hormone (LH) administration, numerous mature oocytes could be obtained and a healthy baby delivered. CASE PRESENTATION: During controlled ovarian stimulation (COS) with only recombinant follicular stimulating hormone (rFSH) administrations, a 26-year-old Japanese woman with hypothalamic amenorrhea (i.e., hypogonadotropic hypogonadism) developed numerous follicles despite low serum E2, 701 pg/ml, and high progesterone (P4) concentrations, 2.11 ng/ml, on the day of induced ovulation. However, 33 cumulus-oocyte complexes (COCs) were successfully obtained; following the embryo culture, four early embryos and six blastocysts were cryopreserved. This patient received hormone replacement therapy (HRT), during which one of six cryopreserved blastocysts was thawed and transferred into the uterine lumen. The patient became pregnant from the first transfer, went through her pregnancy without any complications, and delivered a healthy male baby in the 39th week. Low E2 concentrations in follicular fluids (FFs) are suggestive that aromatase and/or 17ß-hydroxysteroid dehydrogenase (17ß-HSD) could be low. CONCLUSIONS: Serum E2 concentrations may not be the most important index for oocyte maturation during COS, and suggested that oocyte maturation was in progress even under low serum E2 and high P4 conditions. Even if serum E2 concentrations did not properly increase, numerous mature oocytes could be obtained, resulting in the birth of a healthy baby.


Subject(s)
Estradiol/blood , Hypogonadism/blood , Live Birth , Oocytes , Progesterone/blood , 17-Hydroxysteroid Dehydrogenases/metabolism , Adult , Aromatase/metabolism , Embryo Transfer , Estradiol/therapeutic use , Estrogens/therapeutic use , Female , Fertilization in Vitro , Follicle Stimulating Hormone, Human/therapeutic use , Follicular Fluid/metabolism , Hormone Replacement Therapy , Humans , Hypogonadism/therapy , Infant, Newborn , Male , Ovarian Follicle , Ovulation Induction , Pregnancy , Progesterone/therapeutic use , Progestins/therapeutic use , Recombinant Proteins/therapeutic use , Sperm Injections, Intracytoplasmic
4.
Gynecol Obstet Invest ; 82(3): 294-302, 2017.
Article in English | MEDLINE | ID: mdl-27384958

ABSTRACT

BACKGROUND/AIM: The aim of this study was to evaluate the gene and protein expression of angiotensin type (AT) 1, AT2 receptors in endometriotic lesions and its relation to prostaglandin (PG) synthases. MATERIALS AND METHODS: Endometriosis samples were obtained from 32 patients with endometriotic cysts. Endometrial tissues were obtained during operations for benign gynecological conditions. The expression of the AT1 and AT2 receptor mRNA and that of PG-endoperoxide synthase 2 and microsomal PGE2 synthase-1 (mPGES-1) was examined by quantitative RT-PCR. Immunohistochemical staining was performed for these receptors. RESULTS: AT1 and AT2 receptor proteins were mostly located in endometrial glandular epithelium and some stromal cells. Immunoreactivity of the receptor proteins was observed in both the eutopic endometrium and endometriotic lesions. The AT1/AT2 ratio in endometriotic cysts (median 7.29, range 1.88-187.60) was significantly increased compared with that in the eutopic endometrium in the proliferative-phase in controls (median 1.01, range 0.37-2.09, p < 0.001). There was a relationship between the AT1 mRNA expression and that of mPGES-1 mRNA in the endometriotic cysts (r = 0.394089, p < 0.05). There was a significant relationship between the mRNA expression of the AT2 receptor and that of mPGES-1 in eutopic endometrium of non-endometriotic control (r = 0.610714, p < 0.05). CONCLUSION: Renin-angiotensin system may play an important role in the pathophysiology of endometriosis.


Subject(s)
Endometriosis/metabolism , Endometrium/chemistry , Endometrium/metabolism , Gene Expression , Receptor, Angiotensin, Type 1/analysis , Receptor, Angiotensin, Type 2/analysis , Adult , Angiotensin II , Cyclooxygenase 2/genetics , Endometriosis/pathology , Endometrium/pathology , Epithelium/chemistry , Female , Humans , RNA, Messenger/analysis , Receptor, Angiotensin, Type 1/genetics , Receptor, Angiotensin, Type 2/genetics , Stromal Cells/chemistry
5.
J Obstet Gynaecol Res ; 39(5): 1073-6, 2013 May.
Article in English | MEDLINE | ID: mdl-23278946

ABSTRACT

A 33-year-old, gravida 3, para 2, woman was transferred to our hospital, with acute abdominal pain. Abdominal computed tomography (CT) revealed a cystic lesion accompanied by ring-enhancement between the liver and right kidney with fluid collection in the pelvic cavity. Serum hCG value was 3100 mIU/mL. Transvaginal sonography revealed a pseudo-gestational sac in a thickened endometrium. With a preoperative diagnosis of ectopic pregnancy at 7 weeks of gestation, laparotomy was performed. Following careful removal of clots between the liver and right kidney that contained a gestational sac, continuous bleeding from a defect in the Gerota's fascia of the right kidney was noted. The postoperative course was uneventful and the serum hCG concentration decreased markedly. This case demonstrates that the Gerota's fascia is a possible site of ectopic pregnancy, and that CT can identify a pregnancy in the Gerota's fascia as well as in the liver and spleen.


Subject(s)
Pregnancy, Abdominal/surgery , Abdominal Pain/etiology , Adult , Fascia/pathology , Female , Humans , Kidney/pathology , Laparotomy , Peritoneal Cavity , Pregnancy , Pregnancy, Abdominal/diagnostic imaging , Pregnancy, Abdominal/physiopathology , Tomography, X-Ray Computed , Treatment Outcome , Ultrasonography
6.
Am J Reprod Immunol ; 69(3): 231-9, 2013 Mar.
Article in English | MEDLINE | ID: mdl-23252918

ABSTRACT

PROBLEM: Toll-like receptors (TLRs) are innate immune receptors that mediate the pattern recognition of, and response toward, pathogens and host-derived danger signals. We reported that cyclooxygenase-2 (COX-2) and microsomal prostaglandin E synthase (mPGES) mRNA were expressed in cases of endometriosis. The relationship between COX-2, mPGES-1, and TLR4 in endometriotic lesions has yet to be determined. METHOD OF STUDY: Endometriosis samples were obtained from 37 patients with endometrial cysts. Endometrial tissues were obtained from patients undergoing surgical procedures for benign gynecological conditions. COX-2, mPGES-1, and TLR4 mRNA expressions were examined by real-time quantitative reverse transcription PCR (qRT-PCR) and mPGES-1, and TLR4 protein localization was examined by immunohistochemistry. RESULTS: TLR4 proteins were mostly located to the glandular epithelium. The immunoreactivities of TLR4 and mPGES-1 from endometriosis lesions were significantly higher than those in eutopic endometrium in the proliferative phase. The expression levels of mPGES-1 mRNA in peritoneal endometriosis were higher than those in eutopic endometrium in the proliferative phase. The expression of TLR4 mRNA correlates with that of mPGES-1 mRNA and not with that of COX-2 in endometriotic lesions. CONCLUSION: Relationship between TLR4 and mPGES-1 mRNA in endometriotic lesions indicate that innate immunity may play an important role in the pathogenesis of endometriosis.


Subject(s)
Cyclooxygenase 2/metabolism , Endometriosis/immunology , Intramolecular Oxidoreductases/metabolism , Ovary/immunology , Toll-Like Receptor 4/metabolism , Adult , Cyclooxygenase 2/genetics , Female , Gene Expression Regulation , Humans , Immunity, Innate , Immunohistochemistry , Intramolecular Oxidoreductases/immunology , Middle Aged , Peritoneum/immunology , Peritoneum/pathology , Prostaglandin-E Synthases , Receptor Cross-Talk , Toll-Like Receptor 4/immunology , Young Adult
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