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    Advances in Diagnosis and Treatment of Endometrial Cavity Fluid in Patients with Cesarean Scar Defect
    ZENG Zhong-hong, YANG Yi-hua
    Journal of International Reproductive Health/Family Planning    2022, 41 (6): 519-523.   DOI: 10.12280/gjszjk.20220296
    Abstract3045)   HTML24)    PDF (813KB)(3781)      

    Although cesarean section is an essential and common surgical intervention, it also increases the risk of cesarean scar defect (CSD), which is mainly caused by poor healing of the uterine incision. CSD is often accompanied by endometrial cavity fluid, which seriously interfere the embryos′ microenvironment. There are various therapies for CSD, while the unified, valid and standard therapeutic strategies are still inadequate. In this article, we reviewed the mechanism of endometrial cavity fluid in patients with CSD, as well as the impact on embryo implantation and the clinical strategies of treatment.

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    Analysis of the Embryo Transfer Outcomes after the Second Biopsy for Preimplantation Genetic Testing
    XIE Jia-zi, SHEN Jian-dong, WU Wei, DONG Juan, MA Long, CAI Ling-bo, LIU Jia-yin, WANG Dao-wu
    Journal of International Reproductive Health/Family Planning    2022, 41 (6): 441-445.   DOI: 10.12280/gjszjk.20220339
    Abstract3002)   HTML524)    PDF (858KB)(3869)      

    Objective: To evaluate the clinical value of the re-biopsied blastocysts after the first test-unknown preimplantation genetic testing (PGT) cycles, and the effect of the re-biopsied blastocysts on the clinical outcomes of embryo transfer. Methods: The pregnancy outcomes of the 107 re-biopsied blastocysts after the first test-unknown of 75 PGT cycles of 2 199 PGT cycles from September 2015 to May 2021 in the clinical reproductive center of The First Affiliated Hospital with Nanjing Medical University were retrospectively analyzed. Results: In 75 PGT cycles, 107 blastocysts were categorized as unknown diagnosis. Among them, 96 embryos were resuscitated and biopsied, and PGT was successfully carried out in 86 embryos finally. After next-generation sequencing analysis, 46 blastocysts were confirmed as transplantable embryos (39 euploid embryos and 7 chimeric embryos). In 27 warming cycles, 24 blastocysts were survived and entered the transfer cycle. After the second biopsy, the survival rate of embryo resuscitation was 88.89% (24/27), the clinical pregnancy rate 50% (12/24), and the live birth rate 45.8% (11/24). There was one case of early abortion. Conclusions: The blastocysts with unknown diagnosis in the first round of PGT could withstand the second round of biopsy, freezing and resuscitation, and still possessing certain transferable embryos and live birth rate after transplantation.

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    A Clinical Analysis of 13 Cases of Ovarian Sertoli-Leydig Cell Tumor
    XU Qian, CHENG Jiu-mei
    Journal of International Reproductive Health/Family Planning    2022, 41 (4): 279-283.   DOI: 10.12280/gjszjk.20220156
    Abstract2936)   HTML25)    PDF (3265KB)(5195)      

    Objective: To improve the diagnosis and treatment of ovarian Sertoli-Leydig cell tumor (SLCT). Methods: Thirteen cases of ovarian SLCT admitted between June 2014 and July 2021 were analyzed retrospectively, including their clinical characteristics, diagnosis, treatment and prognosis. Results: The median age of onset was 31 years (13-72 years) in 13 patients. Eight patients (61.5%) had the androgenic manifestations (due to the elevated levels of testosterone), 3 patients (23.1%) presented with abnormal uterine bleeding, and the other two patients (15.4%) had no obvious clinical symptoms. Imaging mainly showed cystic-solid tumors or solid tumors. All 13 patients underwent surgery, and diagnosed with ovarian SLCT by histopathology and immunohistochemistry. Eleven patients were at stage ⅠA, and 2 patients at stage ⅠC. Four patients underwent the complementary surgery to resect the affected adnexa and perform the multi-point pelvic and abdominal biopsy after 1-2 months of the initial operation and histopathological diagnosis. Two patients with SLCT at stage ⅠC underwent postoperative chemotherapy with the bleomycin + etoposide + cisplatin (BEP) regimen. The median follow-up time after surgery was 33 months. None of the 13 patients had a recurrence. Conclusions: Ovarian SLCT should be considered when women had abnormal endocrine symptoms and ovarian cystic-solid or solid masses. Surgery is main treatment for SLCT patient, and operative and postoperative histopathology will confirm the diagnosis of ovarian SLCT. Postoperative chemotherapy can be accordingly considered, and the postoperative multidisciplinary follow-up has been suggested.

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    A Case of Successful Delivery in An Infertile Patient with Ovarian Resistance Syndrome: Treated with Antagonist Protocol and Fresh-Embryo Transfer
    CHEN Ya-nan, GUO Jia-li, LI Ze-wu, YANG Ai-jun
    Journal of International Reproductive Health/Family Planning    2022, 41 (4): 294-297.   DOI: 10.12280/gjszjk.20210634
    Abstract2913)   HTML29)    PDF (752KB)(5231)      

    Resistant ovarian syndrome (ROS) is a reproductive endocrine disorder of unknown etiology, with a low incidence and mainly leading to infertility. The complicated treatment and long procedure cause the anxiety of ROS patients. In this paper, we report a case of an infertile patient with ROS, who underwent in vitro fertilization and embryo transfer (IVF-ET) for successful pregnancy. The patient had failed to conceive after several in vitro fertilization treatments at an outside hospital because of her primary infertility, ineffective ovulation treatment, and low response to exogenous gonadotropin (Gn). In the following treatment in our hospital, we adjusted her Gn level and finally obtained a live birth after fresh embryo transfer with an antagonist regimen. Through a retrospective analysis of the relevant literatures, we hope to explore the possible reasons for the successful treatment of this ROS case, and to provide new ideas for the clinical management of ROS patients, so that we can achieve a more satisfactory pregnancy outcome while reducing the cost of treatment.

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    Male Azoospermia Caused by Compound Heterozygous Mutation in CYP21A2 Gene and Multi-Gene Mutations: A Case Report and Literature Review
    GONG Yi-xin, DING Yu, LUO Si-hui, ZHENG Xue-ying
    Journal of International Reproductive Health/Family Planning    2022, 41 (4): 284-288.   DOI: 10.12280/gjszjk.20220207
    Abstract2874)   HTML18)    PDF (3989KB)(5364)      

    CYP21A2 mutation causes 21-hydroxylase deficiency (21-OHD), leading to congenital adrenal hyperplasia and gonadal dysplasia. There is heterogeneity in clinical phenotype due to the different gene mutation sites. Infertility appears to be the leading cause for adult 21-OHD outpatients. The complicated cases of the CYP21A2 mutation combined with multiple gene mutations were rarely reported in the worldwide. We reported a case of male azoospermia with the compound heterozygous mutation of c.518T>A/c.293-13A>G coding CYP21A2. Interestingly, this case was complicated with DNAJB13/DNAI1/QRICH2J/FSIP2/HYDIN multi-gene mutations. The clinical phenotype was male infertility, and spermatogenesis was established by the treatment with glucocorticoid for three months. This case report enriched the genotypes of male infertility, and provided us with experience in the clinical diagnosis and treatment of these diseases.

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    Effect of the Descend Range of Estradiol after Oocyte Retrieval in Antagonist Regimen on the Outcome of In Vitro Fertilization and Embryo Transfer
    ZHOU Yu-xi, ZHANG Juan, ZHANG Juan-juan, LING Xiu-feng, ZHAO Chun
    Journal of International Reproductive Health/Family Planning    2022, 41 (4): 265-269.   DOI: 10.12280/gjszjk.20220104
    Abstract2829)   HTML182)    PDF (853KB)(5182)      

    Objective: To study the effect of the descend range of estradiol (E2) at 48 h after oocyte retrieval compared with 24 h before oocyte retrieval on the pregnancy outcomes of fresh embryo transfer in the antagonist regimen. Methods: A retrospective study was done on the clinical data from 413 cycles of fresh embryo transfer, from January 2017 to March 2021. According to the descend range of E2 48 h after oocyte retrieval compared with 24 h before oocyte retrieval, they were divided into four groups according to the quartile method. Group A: The descend range is 0-25.0% of the overall descend range; Group B: 25.1%-50.0%; Group C: 50.1%-75.0%; Group D: 75.1%-100.0%. The ovulation induction, embryological outcome and pregnancy outcomes were compared, and the relationship between E2 reduction and live birth rates was analyzed by logistic regression. Results: There were significant differences in the total amount of Gn, days of antagonist use, live birth rates, implantation rates and clinical pregnancy rates among the four groups (all P<0.05). The live birth rate of group A was higher than group D, group B was higher than those of group C and group D, and the implantation rates of group A and group B were higher than group D (all P<0.008 3). After adjusting for the factors of differences among groups, the live birth rates of groups A and B were significantly higher than those of group D (OR=2.079, 95%CI: 1.138-3.799, P=0.017; OR=2.187, 95%CI: 1.213-3.944, P=0.009). Conclusions: In the antagonist regimen, the live birth rate of fresh embryo transfer in patients with a greater descend range of E2 at 48 h after oocyte retrieval is lower than that in patients with less descend range of E2.

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    Application of Chromosome Karyotype Analysis and CNV-Seq in Fetals with Increased Nuchal Translucency
    HU Yan-ping, YUAN Jing, LI Qin, ZHOU Pei, CHENG Long-feng
    Journal of International Reproductive Health/Family Planning    2022, 41 (5): 360-364.   DOI: 10.12280/gjszjk.20220224
    Abstract2805)   HTML27)    PDF (800KB)(4367)      

    Objective: To summarize the application of chromosome karyotype analysis combined with copy number variation sequencing (CNV-seq) in the fetuses with increased nuchal translucency (NT). Methods: Karyotype analysis and CNV-seq were performed in 189 singleton fetuses with NT≥2.5 mm and gestation weeks from 11 to 13+6, and the detection rate of chromosomal abnormalities was analyzed. According to the pre-interventional diagnosis indications, they were divided into the simple NT thickening group (n=119) and the non-simple NT thickening group (n=70). According to the NT thickness, they were divided into the 2.5 mm≤NT<3.5 mm group (n=123) and the NT≥3.5 mm group (n=66). Results: Karyotype analysis revealed 31 cases (16.40%) of chromosome abnormalities, including 24 cases (12.70%) of aneuploidy and 7 cases (3.70%) of structural abnormalities, and CNV-seq revealed 38 cases (20.11%) of pathogenic copy number variations (pCNVs), including 24 cases (12.70%) of aneuploidy and 14 cases (7.41%) of other pCNVs. Nine additional cases (5.70%) of pCNVs were detected by CNV-seq in fetuses with normal karyotype. The detection rates of pCNVs and chromosome aneuploidy in the non-simple NT thickening group were higher than those in the simple NT thickening group, and the differences were statistically significant (P<0.05). There was no significant difference in the detection rates of other pCNVs (P>0.05). The detection rates of pCNVs and chromosome aneuploidy in the NT≥3.5 mm group were higher than those in the 2.5 mm≤NT<3.5 mm group, the differences were statistically significant (P<0.05). There was no significant difference in the other pCNVs detection rates (P> 0.05). Conclusions: Fetal chromosomal abnormalities were increased with NT thickening or other pre-interventional diagnostic indicators, but they were not significantly associated with other pCNVs. CNV-seq combined karyotype analysis can help to detect the different types of chromosomal abnormalities, to avoid the missed diagnosis of chromosomal structural abnormalities and chromosomal microdeletion/microduplication.

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    Differences in Baseline Characteristics and Pregnancy Outcomes among Infertile Patients with PCOS at Different Degrees of Oligomenorrhea
    LUO Rong, WANG Yu, LIU Yang, GE Hang, WU Xiao-ke
    Journal of International Reproductive Health/Family Planning    2022, 41 (6): 446-451.   DOI: 10.12280/gjszjk.20220203
    Abstract2698)   HTML73)    PDF (926KB)(3855)      

    Objective: To compare the anthropometric indexes, sex hormones and metabolism of infertile patients with polycystic ovary syndrome (PCOS) at different degrees of oligomenorrhea, and to analyze the pregnancy outcomes after the ovulation induction with acupuncture-assisted clomiphene protocol. Methods: 948 participants with oligomenorrhea in PCOSAct clinical trial were selected. According to the days of menstrual cycle, they were divided into 4 groups: 423 cases in the group A (36-59 days), 311 cases in the group B (60-89 days), 167 cases in the group C (90-179 days) and 47 cases in the group D (≥180 days). The anthropometric indexes, sex hormones, glucose and lipid metabolism were compared, and the pregnancy outcomes were analyzed. Results: The longer the menstrual cycle, the higher the body mass index, waist-hip ratio, black acanthosis score, right ovarian volume, luteinizing hormone, luteinizing hormone/follicle-stimulating hormone, total testosterone, free testosterone, free androgen index, fasting plasma glucose, fasting insulin, homeostatic model assessment values for insulin resistance, triglyceride and apolipoprotein B (all P<0.05). The incidences of insulin resistance and metabolic syndrome were also increased with the extension of menstrual cycle (both P<0.05), while the sex hormone-binding globulin, ovulation rate and biochemical pregnancy rate were decreased (all P<0.05). There were no significant differences in the clinical pregnancy rate, live birth rate and the incidence of perinatal adverse events among the groups (all P>0.05). Multivariate binary logistic regression analysis showed that the menstrual cycle was an independent influencing factor for ovulation and biochemical pregnancy in PCOS patients. Conclusions: The more severe the degree of oligomenorrhea (especially more than 90 days), the more prone to endocrine, glucose and lipid metabolism disorders. Oligomenorrhea may affect adversely the pregnancy outcomes.

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    Two Cases of 21-Hydroxylase Deficiency in Reproductive Age Misdiagnosed as Polycystic Ovary Syndrome and Literature Review
    CHI Xue-xiu, GUO Bao-qiang, YU Shan, HE Dong-hua
    Journal of International Reproductive Health/Family Planning    2022, 41 (4): 289-293.   DOI: 10.12280/gjszjk.20210611
    Abstract2686)   HTML23)    PDF (2342KB)(5222)      

    21-hydroxylase deficiency (21-OHD) is one of the most common congenital adrenal hyperplasia. The clinical symptom in part of patients with 21-OHD is atypical, so that 21-OHD is easy to be misdiagnosed or missed diagnosis. In this paper, we report 2 cases of 21-OHD that was misdiagnosed as polycystic ovary syndrome (PCOS) due to menstrual disorder, infertility and hyperandrogenemia. Sanger sequencing showed that one patient carried c.374G>A (p.Arg125His) and c.518T>A (p.Ile173Asn) heterozygous missense mutations, confirming that the mutant gene came from her parents. Another patient carried homozygous missense mutation of c.518T>A (p.Ile173Asn), and the source of mutation was not clear because her relatives were not detected. With the treatment of oral dexamethasone, 2 patients were restored the regular menstruation, and improved the symptoms of hyperandrogenism. One patient got successful pregnancy and childbirth. When women of childbearing age with infertility and hyperandrogenemia were diagnosed as PCOS, and the treatment effect is not good, 21-OHD should be considered. The combination of 17-OHP assay, ACTH excitation test and gene mutation test will be helpful for the definite diagnosis and differential diagnosis.

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    Clinical Treatment Strategies of Repeated Implantation Failure
    WANG Yan, MENG Qing-xia
    Journal of International Reproductive Health/Family Planning    2022, 41 (4): 302-307.   DOI: 10.12280/gjszjk.20220171
    Abstract2657)   HTML25)    PDF (884KB)(5148)      

    The rapid development of assisted reproductive technology has enabled many infertile patients to get successful pregnances through in vitro fertilization and embryo transfer and its derivative technology. However, there are still some patients who have failed to obtain a clinical pregnancy after transferring high-quality embryos for many times. This is called repeated implantation failure (RIF). RIF is a difficult problem in assisted reproductive technology, which increases the economic burden of patients and aggravates their physical and mental trauma. How to improve embryo quality, to intervene maternal factors (such as improving thin endometrium, improving endometrium receptivity, inhibiting uterine contraction, improving hypercoagulability, immunosuppressive therapy) and to change embryo transfer methods so as to improve pregnancy outcomes, are hot spots in clinical research. The research progress of clinical treatment strategies of RIF due to different etiologies was reviewed in order to provide reference and treatment ideas for clinical workers.

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    The Detrimental Effects of COVID-19 on Human Reproduction
    MAO Xin-yi, XU Yu-wei, LI Wen-jing, MA Zhuo-yao, DING Zhi-de
    Journal of International Reproductive Health/Family Planning    2022, 41 (6): 476-481.   DOI: 10.12280/gjszjk.20220406
    Abstract2635)   HTML75)    PDF (974KB)(3844)      

    The research related to the detrimental effect of COVID-19 has not been limited in the respiratory system, but it gradually expanded to other important systems. Several studies demonstrated that SARS-CoV-2 recognized the angiotensin converting enzyme 2 (ACE2) receptors in human tissues and organs, thereby causing damages to the structure and function of human systems including reproduction. For male reproductive system, SARS-CoV-2 affects the function of hypothalamic-pituitary-gonad (HPG) axis, damages the spermatogenic process and decreases sperm quality. For female reproductive system, SARS-CoV-2 also disturbes the function of HPG axis. Considering the pregnant women infected with the virus, the rate of severe diseases was low and the rehabilitation was good, but adverse pregnancy outcomes may also occur. The impact of SARS-CoV-2 on assisted-reproduction is mild, but it could be a risk factor of pulmonary and renal complications when the patient suffered from ovarian hyperstimulation syndrome during ovulation induction. In addition, there is no evidence to show the obvious negative effect of various SARS-CoV-2 vaccines on the reproductive system. However, mental health problems such as the decreased fertility intention caused by the COVID-19 pandemic still need to be further investigated.

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    Influencing Factors of Psychological Resilience in Infertile Patients with Obese Polycystic Ovary Syndrome
    LYU Xiang-yang, REN Xiao-shuang, ZHANG Liang, XU Ji-qun, WU Hai-cui
    Journal of International Reproductive Health/Family Planning    2022, 41 (6): 452-455.   DOI: 10.12280/gjszjk.20220181
    Abstract2619)   HTML46)    PDF (873KB)(3901)      

    Objective: To investigate the psychological resilience and its influencing factors in infertile patients with obese polycystic ovary syndrome (PCOS). Methods: A total of 235 infertile patients with obese PCOS from the Affiliated Hospital of Shandong University of Traditional Chinese Medicine (our hospital), from January 2019 to August 2021, were selected as the observation group, and 100 healthy adult women who underwent physical examination in our hospital were selected as the control group. The Connor-Davidson Resilience Scale (CD-RISC) was used to assess the psychological resilience. The Fertility Problem Inventory (FPI) was used to assess the infertility-related stress level. The Social Support Rating Scale (SSRS) was used to evaluate the degree of social support of the subjects. The influencing factors of mental toughness were analyzed by the binary Logistic regression. Results: The total scores of CD-RISC and SSRS in the observation group was lower than those in the control group, and the total score of FPI was higher than that in the control group (P<0.05). There were significant differences in CD-RISC score in terms of years of infertility, educational level, and per capita monthly income between the two groups (all P<0.05). The Logistic regression analysis showed that infertility years ≥5, the education level of junior college or below, FPI score<37 were independent risk factors leading to psychological resilience (all P<0.05), while menthly income≥6 000, total SSRS score≥39 were protective factors of psychological resilience (all P<0.05). Conclusions: The psychological resilience of obese PCOS infertility patients is lower than that of the normal population. The PCOS infertility patients with low education level, low monthly income level, low social support level, long infertility years and high infertility related pressure should be actively given psychological intervention.

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    Advances in Pinopodes for Endometrial Receptivity Assessment
    XIANG Yi-ning, FENG Wei-wei
    Journal of International Reproductive Health/Family Planning    2022, 41 (5): 414-418.   DOI: 10.12280/gjszjk.20220250
    Abstract2590)   HTML20)    PDF (795KB)(4281)      

    Successful embryo implantation is a complex process, which is well regulated by both embryo and endometrium. The precise synchronization between the blastocyst and maternal endometrium is very important. Pinopode, a special cellular process expressed in the endometrium, shows different morphologies with the menstrual cycle, which can be divided into the developing pinopode, the maturated pinopode and the degeneration pinopode. A series of clinical studies have proved that the number, the size of coverage area and the development stage of pinopodes have clinical value in predicting the implantation window and assessing the endometrial receptivity in infertile women. Women with higher pinopode score and wider coverage size of pinopodes, and higher proportion of well developed pinopodes, will have better pregnancy outcomes. The mechanism may include that pinopodes affect the endometrial receptivity by regulating uterine contents, and that pinopodes participate in the blastocyst-endometrial interaction by expressing implant-related proteins. However, the accurate and objective assessment method of pinopode still needs to be explored, while the accuracy of its assessment of endometrial receptivity also needs to be further evaluated.

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    Application of Preimplantation Genetic Testing in Assisted Reproductive Therapy for Couples with Sex Chromosome Abnormalities
    SHEN Jian-dong, XIE Jia-zi, WU Wei, CAI Ling-bo, WANG Dao-wu, LIU Jia-yin, DIAO Fei-yang
    Journal of International Reproductive Health/Family Planning    2022, 41 (5): 353-359.   DOI: 10.12280/gjszjk.20220299
    Abstract2581)   HTML59)    PDF (2186KB)(4354)      

    Objective: To analyze the outcomes of preimplantation genetic testing (PGT) in infertile couples with sex chromosome abnormalities and to explore the risk of embryo sex chromosome abnormalities, so as to evaluate the application value of PGT in the related populations. Methods: The embryo chromosome and embryo transfer outcomes of couples with sex chromosome abnormalities treated with PGT were analyzed retrospectively. The whole genome low depth sequencing was used to analyze the alterations of chromosomal copy number after whole genome amplification of biopsy material from the blastocyst stage. In the freeze-thaw cycles, the clinical pregnancy outcomes of embryo transfer were calculated. Results: A total of 77 detectable blastocysts were obtained in 24 controlled ovulation stimulation cycles from 23 couples with sex chromosome abnormalities, including 6 couples with 47,XYY and mosaicism, 2 couples with 47,XXY and mosaicism, 4 couples with 47,XXX, 8 couples with 45,X mosaicism, 3 couples with X-chromosomal segmental aneuploidy. In 77 detectable blastocysts, 76 (98.70%) were definitively diagnosed, including 40 (52.63%) euploid, 13 (17.10%) mosaic embryos and 23 (30.26%) completely aneuploid embryos. All of abnormal embryos were X-chromosomal segmental aneuploidy in the 3 patients with X-chromosomal segmental aneuploidy; whereas a total of 3(3.95%) sex chromosome mosaic aneuploidies were found in the couples with the other sex chromosome numerical abnormality. Nine (50.00%) healthy live births were obtained during a total of 18 freeze-thaw cycles. Conclusions: The couples with sex chromosome numerical aneuploidy have a low risk of embryonic sex chromosome abnormalities, and PGT is not an essential treatment option; whereas the couples with sex chromosome segmental aneuploidy are at high risk of embryonic sex chromosome abnormalities, and PGT may be considered in combination with ovarian function profile and adequate informed consent from the patients, reducing the risk of sex chromosome abnormalities in offspring.

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    A Case Report of Second Cesarean Scar Pregnancy with Intrauterine Device Complicated with Giant Hysteromyoma, Treated by HIFU Combined with Curettage
    HE Meng, HU Meng-ying, DONG Qu-long, YANG Zhen-hua, ZHANG Yan
    Journal of International Reproductive Health/Family Planning    2022, 41 (6): 464-467.   DOI: 10.12280/gjszjk.20220319
    Abstract2563)   HTML32)    PDF (1343KB)(3856)      

    As a special type of ectopic pregnancies, cesarean scar pregnancy (CSP) has a high risk of severe adverse outcomes when untimely diagnosis and treatment occur. It is very necessary to identify it as soon as possible. In recent years, with the application of high intensity focused ultrasound (HIFU) in the field of obstetrics and gynecology, the reports of using HIFU to treat CSP are increasing. However, its application in treating the CSP with intrauterine device has not yet reported. We reported a case of second CSP with intrauterine device complicated with giant hysteromyoma. The patient was hospitalized in our hospital in 2021, who was cured by HIFU combined with curettage. In this case, the clinical treatment is more difficult, surgery alone will face a higher risk of clinical complications. However, HIFU combined with curettage not only achieved the effective treatment of CSP and hysteromyoma, but also minimized the trauma, cost and pain of patients.

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    Case Report of Pregnancy in Two Patients with Diminished Ovarian Reserve Treated with Traditional and Western Medicine, and Literature Review
    ZHANG Yu, XIA Tian
    Journal of International Reproductive Health/Family Planning    2022, 41 (6): 460-463.   DOI: 10.12280/gjszjk.20220234
    Abstract2552)   HTML54)    PDF (789KB)(3812)      

    The diminished ovarian reserve (DOR) is one of the main causes of infertility caused by ovarian factors. The clinical treatment with Western Medicine mainly relies on the oral drugs to improve the ovarian reserve function, artificial hormone cycle replacement and assisted reproductive technology to help pregnancy. The method of Tonifying Kidney and Strengthen Spleen Therapy in Traditional Chinese Medicine (TCM) has many advantages in improving the ovarian reserve function, such as low adverse reactions, long-lasting curative effect and diversified methods. In this article, two cases of DOR patients were reported who were successfully treated with the comprehensive treatment of Tonifying Kidney and Strengthen Spleen Therapy of TCM on the basis of conventional Western Medicine. We emphasized the importance of formulating a targeted and individualized treatment plan of the integrated TCM and Western Medicine for solving difficult diseases. This article provides a new evidence of the comprehensive treatment with TCM and Western Medicine in DOR patients.

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    Dissecting Leiomyoma of The Uterus: A Case Report and Literature Review
    LIU Shuai, LIU Jun, ZHANG Hong-kai, ZHU Mei
    Journal of International Reproductive Health/Family Planning    2022, 41 (5): 396-399.   DOI: 10.12280/gjszjk.20220174
    Abstract2533)   HTML20)    PDF (4138KB)(4302)      

    Dissecting leiomyoma of the uterus is a rare benign leiomyoma with the special growth pattern, no special clinical symptoms and no special manifestations in supplementary examinations. The definite diagnosis requires the postoperative pathology and further immunohistochemical examination. We reported a case of dissecting leiomyoma of the uterus, and retrospectively analyzed the clinical data. In this case, the patient was a perimenopausal female and her annual physical examinations showed that the uterine leiomyoma gradually grew, accompanied by excessive menstruation. Pelvic ultrasound and magnetic resonance imaging results showed uterine leiomyoma with normal tumor markers. Transabdominal myomectomy was performed, and the postoperative pathological diagnosis was dissecting leiomyoma of the uterus.

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    Research Progress of GnRHa Downregulated Hormone Replacement Treatment Cycle in Frozen-Thawed Embryo Transfer
    DUAN Xia, WANG Zhi-hong
    Journal of International Reproductive Health/Family Planning    2022, 41 (5): 419-424.   DOI: 10.12280/gjszjk.20220236
    Abstract2529)   HTML12)    PDF (818KB)(4907)      

    Freeze-thawed embryo transfer (FET) has been widely used in clinical practice due to its advantages of the increasing cumulative pregnancy rate and the reducing risk of ovarian hyperstimulation. The quality of transplanted embryos, endometrium and their synchronization are the key factors of FET success. The common clinical schemes of endometrial preparation include natural cycle, controlled ovarian stimulation, hormone replacement treatment (HRT) and downregulation HRT. For the most women, the above conventional schemes can be used for FET endometrial preparation. For special patients such as the patients with polycystic ovary syndrome, endometriosis, adenomyosis, recurrent implantation failure and thin endometrium, the clinical effect of conventional endometrial preparation scheme is poor. The pituitary downregulation method is based on the GnRHa pituitary downregulation, and hormone replacement therapy is applied to prepare the endometrium, suggesting that the downregulated HRT cycle can effectively improve the pregnancy outcome of the above special population compared with the conventional endometrial preparation scheme. This paper reviews the related mechanisms of GnRHa down regulation of HRT cycle and its suitable population.

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    A Case of 46,XY Female Sexual Reversal Syndrome and Literature Review
    HE Juan-juan, LIU Kun, WANG Pei-chen, SHEN Meng-dan, ZHANG Xue-hong
    Journal of International Reproductive Health/Family Planning    2022, 41 (5): 386-388.   DOI: 10.12280/gjszjk.20220259
    Abstract2527)   HTML17)    PDF (2212KB)(4308)      

    By reviewing the clinical data of an adolescent female with primary amenorrhea, including the abdominal color ultrasound, chromosomal karyotype and peripheral blood chromosomal aberration detection (chip) analysis, and by reviewing the related literature, we discussed the clinical etiology, diagnosis and treatment of 46,XY female sex inversion. Abdominal color ultrasound showed no sexual organs; karyotype was 46,X,max?; and chromosomal aberration detection (chip) analysis of peripheral blood was 46,XY. Therefore, the clinical etiology of this child is related to the abnormal process of chromosomal sex-determining gonadal differentiation. Traditional karyotype detection has certain limitations, and the peripheral blood chromosomal aberration detection (chip) analysis can be used to identify the cause.

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    Autophagy in Mechanism of Ovulatory Dysfunction Infertility
    ZHANG Lei, LIANG Lin-lin, FENG Ke, MENG Li, ZHANG Cui-lian
    Journal of International Reproductive Health/Family Planning    2022, 41 (6): 504-508.   DOI: 10.12280/gjszjk.20220335
    Abstract2527)   HTML34)    PDF (849KB)(3866)      

    Ovulatory dysfunction infertility, a common type of infertility, is due to the anovulation or oligo-ovulation because of endocrine disorders, chromosomal and genetic abnormalities, drug toxicity, ovarian lesions and other factors, which affect the combination of sperm and oocytes. Autophagy is an important way for the degradation and reuse of cell components. It occurs in a variety of physiological and pathological processes, including ovarian reserve, follicular development and atresia. Studies have shown that the abnormal autophagy in the ovary results in a variety of diseases causing ovulation disorders. For example, the autophagy activity is increased in polycystic ovary syndrome, abnormally increased or decreased in premature ovarian insufficiency and premature ovarian failure, and suppressed in ovarian endometriosis cysts. Multiple signaling pathways including mTOR are involved in the regulation of autophagy in follicular granulosa cells and oocytes. Deletion and mutation of key autophagy factors, as well as over activation, affect the proliferation, apoptosis and secretion of follicular cells, thus hindering the normal development and ovulation of follicles. Metformin and some hormone drugs can participate in the regulation of autophagy. In conclusion, autophagy may play a role in the development of ovulatory dysfunction infertility.

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