Over the years, I have worked in a diverse field of Obstetrics and Gynecology (Obstetrics, Gynecologic Oncology, Reproductive Immunology, etc.).
Currently, I am exploring care/support for women throughout their lifetime, based on obstetrics and gynecology. I am involved in research on topics related to pregnancy, childbirth, and childcare, as well as women's health and mental health.
Biography: Born in 1965 in Aomori Prefecture, graduated from Hokkaido University School of Medicine in 1990, completed graduate studies at Hokkaido University Graduate School of Medicine in 1997, worked as an assistant at Hokkaido University Hospital in 2000, became a lecturer at Kobe University Graduate School of Medicine in 2010, and an associate professor in 2012, from 2020. Professor, Graduate School of Health Sciences, Hokkaido University (Department of Midwifery/Maternal Nursing/Women's Medical Science, Division of Developmental Nursing). Doctor of Medicine (Hokkaido University)
Synopsis The frequency of non-puerperal uterine inversion is rare. Non-puerperal incomplete uterine inversion was diagnosed in a 52-year-old woman (gravida 2, para 2, not yet menopausal). She was diagnosed with uterine myoma at 47 years old. She visited a GYN clinic because of irregular vaginal bleeding at 50 years old, and repeated GnRHa treatment was selected. However, the size of the uterine myoma could not be reduced, and the patient was referred to our hospital for operative treatment. The chief complaint at the initial visit was a generous amount of vaginal discharge. The diagnosis of non-puerperal incomplete uterine inversion was made according to MRI findings of an inverted fundus and prolapsed submucous myoma in the vagina. Abdominal total hysterectomy and bilateral fallopian tubal resection were performed. The pathological diagnosis was submucous uterine leiomyoma. The postoperative course was uneventful and the symptom of discharge disappeared. [Adv Obstet Gynecol, 69 (2) : 126-130, 2017 (H29.5)]
We present a case of complete androgen insensitivity syndrome (CAIS) treated by laparoscopic gonadectomy. Case: A 19-year-old phenotypical female, who complained of primary amenorrhea, was referred to our hospital. Physical examination revealed the absence of the proximal vagina and female external genitalia. Pelvic magnetic resonance imaging revealed bilateral pelvic masses, and the absence of both the uterus and the vagina. Hormonal examination revealed elevated serum testosterone level at 8.3 ng/mL (normal values in female adults, 0.06-0.86 ng/mL). Her karyotype was 46,XY. Therefore, we diagnosed complete CAIS. She underwent laparoscopic gonadectomy. Histopathological examination showed immature seminiferous tubules and Leydig cells in both gonads. Her postoperative course was uneventful and she was discharged on postoperative day 5. She is being treated with and will continue to receive hormone replacement. Care for patients with CAIS needs to be individualized, flexible, and holistic because they are often raised socially as women. Laparoscopic gonadectomy in patients with CAIS is useful, because it is less invasive and has improved cosmetic results compared with open surgery.