ADVANCES IN OBSTETRICS AND GYNECOLOGY
Online ISSN : 1347-6742
Print ISSN : 0370-8446
ISSN-L : 0370-8446
Volume 63, Issue 3
Displaying 1-50 of 60 articles from this issue
ARTICLES
Original
  • Tomonobu TAKEI, Koji NAKABAYASHI, Naoya TAKEMURA, Natsuko MAKIHARA, Ka ...
    2011 Volume 63 Issue 3 Pages 271-276
    Published: 2011
    Released on J-STAGE: October 03, 2011
    JOURNAL RESTRICTED ACCESS
    This study was conducted to establish the strategy for diagnosis of deep vein thrombosis (DVT)in women with ovarian tumors before surgery in Kobe University Hospital. Medical charts of 193 women with ovarian tumors who had undergone surgery in Kobe University Hospital between January 2006 and June 2010 were systemically reviewed. Pathological examinations identified 115 cases with benign ovarian tumors, 15 cases with borderline malignancy and 63 cases with malignant ovarian tumors. Clinical and laboratory data were compared between patients diagnosed as having DVT and those with no evidence of DVT. Venous ultrasound imaging of the lower extremity was performed in 32 out of 193 patients. 18 out of 32 patients were diagnosed as having DVT before surgery, including 5 cases with benign ovarian tumors, 2 cases with borderline malignancy, and 11 cases with malignant ovarian tumors. The statistical analyses were performed between DVT patients and non-DVT patients in terms of benign-malignancy, ages, with or without symptoms, tumor maximum diameters, plasma D-dimer levels and BMI. The incidence of DVT was significantly higher in patients with malignant ovarian tumors compared with those with benign ovarian tumors. The incidence of DVT was not correlated with ages. The symptom such as limb pains, edema in the lower extremity clearly indicated the DVT existence compared with no symptom. The tumor maximum diameters had no significant differences in between DVT patients and non-DVT patients. But plasma D-dimer levels were significantly higher in patients with DVT than in those without DVT. Plasma D-dimer levels were found to be more than 3.0 μg/ml in all 18 cases with DVT. 12 out of 18 cases with DVT had symptoms. However, venous ultrasound imaging of the lower extremity demonstrated no findings of DVT in 6 patients who had both limb pains and plasma D-dimer levels less than 3.0μg/ml. In conclusion, the diagnosis of DVT by venous ultrasonography should be done in patients with ovarian tumors when their plasma D-dimer levels were at least more than 3.0μg/ml. [Adv Obstet Gynecol, 63(3) : 271-276, 2011 (H23.8)]
    Download PDF (1099K)
  • Aya HARADA, Noriomi MATSUMURA, Fumimasa KOBAYASHI, Tsukasa BABA, Ayako ...
    2011 Volume 63 Issue 3 Pages 277-283
    Published: 2011
    Released on J-STAGE: October 03, 2011
    JOURNAL RESTRICTED ACCESS
    Treatment with pegylated liposomal doxorubicin (PLD)was initiated for heavily treated patients with recurrent ovarian cancer (n=13)and peritoneal cancer (n=4)from July 2009 through June 2010 in our hospital. We experienced complete response in 1 case and partial response in 3 cases, with a response rate of 27% (4/15). Adverse effects included stomatitis (53%), hand-foot syndrome (71%), and myelosuppression (88%), but were not severe. The period from onset of the primary disease until PLD treatment (> 2 years)correlated with the anti-tumor effect of PLD, which implies that tumors in which previous chemotherapy had been effective are sensitive to PLD. Stomatitis also correlated with a tumor response (p<0.05). Although the overall anti-tumor effect in three cases that needed periodic removal of ascites prior to the PLD treatment was progressive disease, the retention of ascites in these three cases decreased prominently with the intravenous administration of PLD. Further study is desired to establish a protocol for the treatment of recurrent ovarian and peritoneal cancer by accumulating clinical data on the use of PLD in Japan from now on. [Adv Obstet Gynecol, 63(3) : 277-283, 2011 (H23.8)]
    Download PDF (468K)
Clinical Report
  • Akimasa TAKAHASHI, Marisa TERAI, Haruta MOGAMI, Yumiko SATAKE, Satoko ...
    2011 Volume 63 Issue 3 Pages 284-288
    Published: 2011
    Released on J-STAGE: October 03, 2011
    JOURNAL RESTRICTED ACCESS
    The HELLP syndrome (HELLP), a serious complication of pregnancy, derives its name from the main findings of hemolysis, elevated liver enzymes and a low platelet count. Very few Japanese studies have been conducted comparing between antepartum and postpartum HELLP. We conducted a retrospective study of 9 women treated over the past 7 years, surveying maternal outcomes, complications, treatments and the time of onset. Pregnancy induced hypertension was also present in all 9 patients, and all were delivered by Caesarean section at 32~40 weeks of gestation. The onset of HELLP was prior to delivery in 6 cases (66.7%), with the remaining 3 cases developing within 4 days after delivery. Using the Tennessee Classification System, all 3 cases with postpartum HELLP were complete, whereas 2 of the 6 cases with antepartum HELLP were incomplete. Laboratory investigations revealed significantly higher serum AST levels in patients with postpartum HELLP than those with antepartum onset. Although the difference was not significant, platelet counts tended to be lower, and LDH levels higher, in patients with postpartum HELLP. Serious maternal complications such as acute pulmonary edema, acute renal failure or massive ascites were observed only in patients with postpartum HELLP, indicating that postpartum HELLP is more likely to be severe than disease of antepartum onset. [Adv Obstet Gynecol, 63(3) : 284-288, 2011(H23.8)]
    Download PDF (690K)
Case Report
  • Yuki YAMADA, Hidekazu OI, Kana IWAI, Emiko NIIRO, Sachiko MORIOKA, Emi ...
    2011 Volume 63 Issue 3 Pages 289-294
    Published: 2011
    Released on J-STAGE: October 03, 2011
    JOURNAL RESTRICTED ACCESS
    The rapid growth of recurrent adult granulosa cell tumor at the beginning of menstruation in the puerperium: a case report Granulosa cell tumors (GCTs)of the ovary are low-grade ovarian malignancies with a predilection for late recurrences in the pelvic cavity and occasionally distant metastases. They represent only 2-5% of all ovarian cancers. A right intra-pelvic mass was detected by ultrasound in a 29-year-old woman in the first trimester of pregnancy who was diagnosed with adult GCT (AGCT)pT1c(a)NXMO at the time of a right adenectomy for an adnexal mass 2 years before. The right intra-pelvic mass was resected 80% at 20 weeks of gestation and was confirmed to be a recurrent AGCT pathologically. The growth of residual tumors was evaluated by diffusion-weighted MR imaging during the pregnancy. The tumor size was correctly confirmed by this technique to have not changed. Cesarean section with suboptimal tumor reduction surgery excluding the tumors near the ileocecal region was performed at 37 weeks of gestation. No further treatment was performed after the cesarean section. Regarding tumor size, the tumor in the Morison cavity had rapidly grown by the beginning of the menstruation in the puerperium. Optimal tumor debulking including partial ileotomy was agreed upon and performed. The findings in this case were considered to correlate with hormone dependency, so hormone therapy may be a viable treatment option for any further recurrence. Several recent case reports have indeed raised the possibility of the use of hormonal therapy in the management of recurrent GCT. [Adv Obstet Gynecol, 63(3) : 289-294, 2011 (H23.8)]
    Download PDF (656K)
  • Masanori ISOBE, Yong-kok KIM, Ayako HOSOI, Takahito MIYAKE, Yasuhiko S ...
    2011 Volume 63 Issue 3 Pages 295-300
    Published: 2011
    Released on J-STAGE: October 03, 2011
    JOURNAL RESTRICTED ACCESS
    The optimal strategy for salvage therapy in patients who suffer from endometrial cancer recurrence after a disease-free interval has not yet been established. However, recent analyses suggest that in patients with recurrent endometrial cancer, the performance of complete cytoreduction to the point of no gross residual disease is associated with favorable overall survival outcome. Diaphragmatic metastasis of endometrial cancer is a rare occurrence. A diaphragmatic mass resection by laparotomy, which requires a large incision is associated with severe pain and a higher risk of perioperative complications. We herein report a case of a laparoscopic resection of diaphragmatic metastasis originating from endometrial cancer. The patient was a 59-year-old female who had undergone radical surgery for FIGO (1988) stage IIIa endometrial cancer, followed by 3 courses of adjuvant chemotherapy. Thereafter, the patient developed an isolated right diaphragmatic metastasis 48 months postoperatively. This patient with disease confined to the diaphragm (diameter, 2.0 cm) was successfully treated by laparoscopy alone, and a full-thickness diaphragmatic resection was performed. No major perioperative complications were encountered. The hospital stay was 7 days postoperatively. The patient received 6 courses of adjuvant chemotherapy and has since been in good health without recurrence for 2 years after adjuvant chemotherapy. A diaphragmatic tumor resection by laparoscopy is a less invasive approach which is technically feasible and safe, while also requiring a short hospital stay. [Adv Obstet Gynecol, 63(3) : 295-300, 2011 (H23.8)]
    Download PDF (1315K)
  • Misako NAKAMURA, Noriko FURUITA, Miyoko WARATANI, Ai TOMINAGA, Takuji ...
    2011 Volume 63 Issue 3 Pages 301-306
    Published: 2011
    Released on J-STAGE: October 03, 2011
    JOURNAL RESTRICTED ACCESS
    In recent years, the number of cancer survivors has been increasing due to the advances in cancer treatment. However, there are limited data on how treatment for cancers such as leukemia and breast cancer affects younger patients who survive pregnancy and childbirth retain their ability to breastfeed, and preserve their fertility. Here, we report 2 cases of pregnancy after breast cancer treatment that were treated at our hospital. [Case1] A 32-year-old woman was diagnosed with Paget's disease during her fifth pregnancy and underwent surgery after delivery. Endocrine chemotherapy consisting of toremifene citrate and 5-fluorouracil (5-FU) was started approximately 2 years after the surgery. She became pregnant during the endocrine chemotherapy, which resulted in miscarriage. She became pregnant again 5 and a half years later, had no complications during the pregnancy, and underwent normal vaginal delivery at 40 weeks' gestation. However, her postpartum lactation was insufficient. [Case2] A 28-year-old woman was diagnosed with invasive ductal cancer of the breast 6 months after vaginal delivery of her first child. Two years after the surgery, chemotherapy with FEC100 and weekly paclitaxel combined with goserelin acetate was started. She received hormone replacement therapy for 3 months after chemotherapy. She became pregnant 3 years and 4 months after the surgery, had no abnormalities during the pregnancy, and underwent normal vaginal delivery at 38 weeks' gestation. She had no problems during delivery and lactation. No disease relapse occurred in both the cases for more than 9 months after delivery. [Adv Obstet Gynecol, 63(3) : 301-306, 2011 (H23.8)]
    Download PDF (618K)
  • Sachiko MORIOKA, Yasuhito TANASE, Kana IWAI, Emiko NIIRO, Yuki YAMADA, ...
    2011 Volume 63 Issue 3 Pages 307-312
    Published: 2011
    Released on J-STAGE: October 03, 2011
    JOURNAL RESTRICTED ACCESS
    Endometriosis is a common gynecological condition mainly involving the pelvic organs. Extragenital endometriosis is less common, but has been observed in almost every area of the female body. This is the case report of an extremely rare case of pubic bone endometriosis that could be treated by laparoscopy-assisted tumorectomy. A 34-year-old nulliparous woman complained of cyclic pain in the groin. Abdominal and vaginal examination findings were unremarkable, however, a mass was found in the right inguinal region, which was confirmed to be not caused by inguinal herniation. It took 3 years to diagnose the pubic bone endometriosis correctly. The patient was offered tumorectomy through an incision in the inguinal region with laparoscopy after conservative medical management using dienogest for 9 months. Both the inguinal tumor and pelvic peritoneum were consistent with a histological diagnosis of endometriosis. Because of its varied presentations, endometriosis remains a difficult condition to diagnose and treat. A possibility of extrapelvic endometriosis exists in case of cyclic pain from pubis to the inguinal area. [Adv Obstet Gynecol, 63(3) : 307-312, 2011 (H23.8)]
    Download PDF (1162K)
  • Kanako HOSONO, Mana TAKI, Kazutoshi INADA, Yumiko MIYAZAKI, Michiko WA ...
    2011 Volume 63 Issue 3 Pages 313-318
    Published: 2011
    Released on J-STAGE: October 03, 2011
    JOURNAL RESTRICTED ACCESS
    Placental mesenchymal dysplasia (PMD)is a rare condition that shows an abnormally enlarged placenta. Ultrasonographic finding of polycystic placenta often leads to the misdiagnosis of partial hydatidiform mole or twin pregnancy with a complete hedatidiform mole and surviving co-existent fetus. Definitive diagnosis usually requires pathological examination. PMD is frequently associated with intrauterine growth restriction or Beckwith-Wiedemann syndrome (BWS). Herein, we describe a case of PMD complicated with anemia and thrombocytopenia of the fetus. A 32-year-old multipara (2G2P) conceived her third child naturally and consulted an obstetric clinic. From the first trimester, multiple cystic lesions in the placenta were noted on ultrasound examination. The size of the placenta, which lay close to the internal os, increased rapidly and the patient felt frequent uterine contraction from 28 weeks of gestation. Possible arrest of the fetal growth was suspected from 33 weeks of gestation and she was admitted to our hospital at 35 weeks and 0day of gestation. Soon thereafter, fetal tachycardia with abnormally elevated middle cerebral artery peak systolic velocity (>1.55MoM), which is indicative of fetal anemia, was noted. Impending fetal cardiac failure due to anemia was suspected and emergency caesarean section was performed at 35 weeks and 2 days of gestasion. A 1980g (-1.2SD)male baby was deliverd. The newborn showd moderate anemia (hemoglobin=7.8g/dl) and thrombocytopenia (plateltets=89000/μl). The placenta weighed 4000g and PMD was diagnosed pathologically. And thrombosis in the placental vessels was shown pathologically, microangiopathic process was likely cause of fetal anemia and thrombocytopenia. There was no detectable sign of BWS. [Adv Obstet Gynecol, 63(3) : 313-318, 2011 (H23.8)]
    Download PDF (977K)
OPINIONS
Clinical view
Current topic
TRANSACTIONS of SECTIONAL MEETING
Gynecologic Oncology (in the 123th Meeting of the OBSTETRICAL GYNECOLOGICAL SOCIETY OF KINKI DISTRICT JAPAN)
"Diagnosis and Treatment of uterine cervical cancer"
Perinatology(in the 123th Meeting of the OBSTETRICAL GYNECOLOGICAL SOCIETY OF KINKI DISTRICT JAPAN)
"Prenatal diagnosis of congenital fetal abnormalities using advanced fetal imaging"
feedback
Top