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1.
J Med Case Rep ; 9: 258, 2015 Nov 17.
Article in English | MEDLINE | ID: mdl-26572791

ABSTRACT

INTRODUCTION: Isolated torsion of the fallopian tube without an ovarian abnormality is an uncommon event, with an incidence of approximately 1 in 1,500,000 females. Isolated torsion of the fallopian tube occurs mostly in reproductive-aged women, and is thus extremely rare in menopausal women and pre-pubertal girls. CASE PRESENTATIONS: In case 1, 63-year-old Japanese woman presented with a 2-day history of acute lower abdominal pain. Menopause occurred at 53 years of age. Pelvic ultrasonography showed an enlarged mass (73 × 47 mm) on the right side of her uterus. An urgent laparoscopy was performed based on a presumptive diagnosis of right ovarian tumor torsion. During the laparoscopy, we noted a black, necrotic, solid tumor arising from the distal end of her right fimbria. Her right fallopian tube was twisted with the tumor, but her right ovary was normal and not involved. A laparoscopic tumorectomy with a right salpingectomy was performed. Her post-operative course was uneventful. In case 2, a 10-year-old Japanese girl presented with a 1-day history of lower abdominal pain associated with nausea and vomiting. Menarche had occurred 2 months earlier. A computed tomography and magnetic resonance imaging examination demonstrated a dilated tubal cystic mass with a normal uterus and bilateral ovaries. An urgent laparoscopy was performed based on a presumptive diagnosis of right fallopian tube torsion. During laparoscopy, her right fallopian tube was noted to be dark red, dilated, and twisted several times. Her right fimbria was necrotic-appearing and could not be preserved. Therefore, a laparoscopic right salpingectomy was performed. A histologic examination revealed ischemic changes with congestion of her right fallopian tube, which was consistent with tubal torsion. She had an uncomplicated post-operative course. CONCLUSION: We have presented two very rare cases of isolated fallopian tubal torsion. Radiologic interventions, such as computed tomography and magnetic resonance imaging, in addition to ultrasonography, are helpful diagnostic tools. Isolated torsion of the fallopian tube should be considered in the differential diagnosis of lower abdominal pain with a cystic mass and a normal ipsilateral ovary in all female patients, regardless of age.


Subject(s)
Fallopian Tube Diseases/diagnosis , Fallopian Tube Diseases/surgery , Fallopian Tubes/pathology , Torsion Abnormality/diagnosis , Torsion Abnormality/surgery , Abdominal Pain/etiology , Child , Female , Humans , Middle Aged , Postmenopause , Salpingectomy , Tomography, X-Ray Computed , Ultrasonography
2.
J Med Case Rep ; 9: 47, 2015 Feb 14.
Article in English | MEDLINE | ID: mdl-25881005

ABSTRACT

INTRODUCTION: Solitary uterine metastases from extragenital cancers are very rare. Breast cancer is the most frequent primary site of metastasis to the uterine corpus, with invasive lobular carcinoma more likely to spread to gynecologic organs than invasive ductal carcinoma. CASE PRESENTATION: A 62-year-old postmenopausal Japanese woman was diagnosed with uterine leiomyomata more than 20 years ago and had been managed conservatively until menopause. Seven years prior to her presentation, she was diagnosed with breast cancer and underwent a partial resection of her right breast for stage IIA invasive lobular carcinoma. She underwent adjuvant chemotherapy, radiotherapy, and five years of anastrozole hormonal therapy. She presented with a growing uterine mass. Her tumor marker levels were markedly increased over the course of her follow-up, but a systemic examination revealed only a solitary uterine tumor. She underwent a total abdominal hysterectomy with bilateral salpingo-oophorectomy. A histopathological examination, including detailed immunohistochemistry, confirmed metastatic invasive lobular carcinoma, infiltrating both her uterine myometrium and fibroid tissue. CONCLUSION: We report a very rare metastatic pattern of invasive lobular carcinoma and demonstrate that gross cystic disease fluid protein-15 and mammaglobin are useful in the diagnosis of metastatic breast cancer.


Subject(s)
Antineoplastic Agents, Hormonal/therapeutic use , Breast Neoplasms/pathology , Carcinoma, Lobular/secondary , Uterine Neoplasms/secondary , Anastrozole , Biomarkers, Tumor/analysis , Carcinoma, Lobular/diagnosis , Carcinoma, Lobular/therapy , Carrier Proteins/analysis , Combined Modality Therapy , Female , Glycoproteins/analysis , Humans , Leiomyoma/therapy , Membrane Transport Proteins , Middle Aged , Nitriles/therapeutic use , Triazoles/therapeutic use , Uterine Neoplasms/therapy
3.
J Med Case Rep ; 9: 84, 2015 Apr 18.
Article in English | MEDLINE | ID: mdl-25902845

ABSTRACT

INTRODUCTION: Spontaneous rupture of an ovarian artery aneurysm is extremely rare. Although a majority of these cases have been associated with pregnancy, there have been recent reports and reviews of rare cases that were not directly associated with pregnancy. Transcatheter arterial embolization is considered to be an alternative therapy to surgery. CASE PRESENTATION: A 44-year-old Japanese woman, gravida 3 para 3, presented to our emergency room complaining of intermittent right flank pain. She had undergone a cesarean section 2 years previously, and had no history of abdominal trauma. On admission, her blood pressure was 115/78 mmHg, pulse 70 beats per minute, and hemoglobin concentration 9.8 g/dL. Abdominal ultrasonography and contrast-enhanced dynamic computed tomography revealed a large retroperitoneal hematoma. Findings on three-dimensional computed tomography angiography suggested ruptured aneurysm of her right ovarian artery. A selective right ovarian artery angiogram revealed a tortuous aneurysm. Transcatheter arterial embolization using N-butyl-2-cyanoacrylate was performed. The aneurysm was successfully embolized, and her course after embolization was uneventful. She has remained symptom-free during 3 months of follow-up. CONCLUSIONS: This was a very rare case of a patient who had a retroperitoneal hemorrhage originating from an ovarian artery aneurysm. A review of published case reports found that contrast-enhanced computed tomography with reconstruction images is an excellent imaging tool. Diagnostic angiography and subsequent transcatheter arterial embolization are thought to be very effective for this condition.


Subject(s)
Aneurysm, Ruptured/complications , Hemorrhage/etiology , Ovary/blood supply , Adult , Aneurysm, Ruptured/therapy , Angiography , Aorta, Abdominal/diagnostic imaging , Contrast Media , Embolization, Therapeutic , Female , Flank Pain/etiology , Humans , Rupture, Spontaneous
4.
BMC Res Notes ; 7: 821, 2014 Nov 20.
Article in English | MEDLINE | ID: mdl-25409709

ABSTRACT

BACKGROUND: Cardiopulmonary arrest in pregnancy has a very high maternal and fetal mortality rate. We report a case of successful maternal and neonatal survival in association with emergency cesarean section of a schizophrenic pregnant patient. To our knowledge, this is the first reported case of cardiopulmonary arrest in a pregnant woman with schizophrenia. CASE PRESENTATION: The parents were Japanese. The mother was 39 years old and had no history of prior pregnancy. Her admission to our hospital at 36 weeks and 4 days of pregnancy was due to deterioration of schizophrenia. On the first day of hospitalization, she collapsed after a seizure and vomiting, and an emergency resuscitation team was called immediately. The team identified apparent aspiration and successfully resuscitated the patient after 11 minutes of cardiopulmonary arrest. An emergency cesarean section was performed in the operating room. The newborn male infant received bag and mask ventilation at birth, and his Apgar scores were 5 at 1 minute and 8 at 5 minutes. He had a myoclonic seizure on the 2nd day of life: however, he experienced no further seizures on anticonvulsant medication after that episode. On the 18th day of life, magnetic resonance imaging of his brain revealed bilateral small hyperintensities on T1-weighted images in the basal ganglia. The mother and her newborn were discharged from our hospital without neurological disorders. CONCLUSION: We speculate that the cause of cardiopulmonary arrest was aspiration due to seizure, and it is possible that a neurological response was evoked by administration of antipsychotic drugs and/or by eclampsia. Medical staff must be aware of the possibility of cardiopulmonary arrest in pregnant women with schizophrenia.


Subject(s)
Heart Arrest/complications , Schizophrenia/complications , Adult , Female , Humans , Infant, Newborn , Magnetic Resonance Imaging , Male , Pregnancy , Radiography, Thoracic
5.
J Obstet Gynaecol Res ; 40(1): 53-61, 2014 Jan.
Article in English | MEDLINE | ID: mdl-23937716

ABSTRACT

AIM: To examine the relationship between preterm birth and socioeconomic factors, past history, cervical length, cervical interleukin-8, bacterial vaginosis, underlying diseases, use of medication, employment status, sex of the fetus and multiple pregnancy. METHODS: In a multicenter, prospective, observational study, 1810 Japanese women registering their future delivery were enrolled at 8⁺° to 12⁺6 weeks of gestation. Data on cervical length and delivery were obtained from 1365 pregnant women. Multivariate logistic regression analysis was performed. RESULTS: Short cervical length, steroid use, multiple pregnancy and male fetus were risk factors for preterm birth before 34 weeks of gestation. Multiple pregnancy, low educational level, short cervical length and part-timer were risk factors for preterm birth before 37 weeks of gestation. CONCLUSION: Multiple pregnancy and cervical shortening at 20-24 weeks of gestation was a stronger risk factor for preterm birth. Any pregnant woman being part-time employee or low educational level, having a male fetus and requiring steroid treatment should be watched for the development of preterm birth.


Subject(s)
Cervix Uteri/pathology , Pregnancy, Multiple , Premature Birth/epidemiology , Steroids/adverse effects , Women, Working , Adult , Cervical Length Measurement , Cervix Uteri/diagnostic imaging , Educational Status , Female , Humans , Incidence , Infant, Newborn , Japan/epidemiology , Male , Organ Size , Pregnancy , Pregnancy Outcome , Premature Birth/chemically induced , Premature Birth/etiology , Premature Birth/pathology , Prevalence , Risk Factors , Sex Characteristics , Socioeconomic Factors
6.
Neurol Med Chir (Tokyo) ; 53(8): 561-4, 2013.
Article in English | MEDLINE | ID: mdl-23979053

ABSTRACT

Moyamoya disease is a rare chronic, occlusive cerebrovascular disease characterized by bilateral steno-occlusive changes at the terminal portion of the internal carotid artery and an abnormal vascular network at the base of the brain. Moyamoya disease particularly affects children and young adults with female predominance, thus pregnant patients with moyamoya disease are not uncommon. Among 4,400 patients with consecutive deliveries in our hospital, 6 patients (0.14%) aged from 24 to 40 years (mean 32.7 years) were found to have moyamoya disease, all of whom underwent cesarean section. Four patients who had been diagnosed with moyamoya disease before pregnancy did not show neurological events in pregnancy and puerperium, but two patients who were newly diagnosed or progressed during the perinatal period suffered neurological deterioration due to ischemic stroke. Surgical revascularization at the subacute stage relieved their symptoms and they did not suffer permanent neurological deficit. We recommend that pregnant patients with moyamoya disease should be carefully managed under the collaboration of obstetricians and neurosurgeons, and that the procedure of the delivery should selected by the obstetricians to avoid unfavorable sequelae caused by hyperventilation and/or blood pressure elevation.


Subject(s)
Moyamoya Disease/surgery , Pregnancy Complications, Cardiovascular/surgery , Adult , Cerebral Angiography , Cerebral Infarction/diagnosis , Cerebral Infarction/surgery , Cerebral Revascularization , Cesarean Section , Cooperative Behavior , Diffusion Magnetic Resonance Imaging , Disease Progression , Female , Humans , Interdisciplinary Communication , Japan , Magnetic Resonance Angiography , Moyamoya Disease/diagnosis , Neurologic Examination , Pregnancy , Pregnancy Complications, Cardiovascular/diagnosis , Stroke/diagnosis
7.
Arch Gynecol Obstet ; 287(5): 1005-8, 2013 May.
Article in English | MEDLINE | ID: mdl-23224652

ABSTRACT

PURPOSE: Postoperative chylous ascites is an unusual complication following retroperitoneal surgery. A search of the English literature showed only 44 cases of chylous ascites following gynecological cancer surgery. The treatment is primarily conservative, but surgical treatment is considered in resistant cases. We developed a novel non-surgical therapeutic strategy for postoperative chylous ascites. METHODS: We report a case of severe chylous ascites following pelvic lymph node dissection for gynecological cancer. RESULTS: Total abdominal hysterectomy, bilateral salpingo-oophorectomy, peritoneal washing, and systematic pelvic lymph node dissection were performed for a stage II G1 endometrioid adenocarcinoma (FIGO 2009). Forty-one days after surgery, the patient was readmitted due to massive ascites. Repeated paracentesis and a low-fat diet were only partially effective. Fifty-one days after surgery, we started paracentesis with a continuous low-pressure drainage system. Nine days later, there was no further fluid drainage. The patient was asymptomatic and without recurrent disease at follow-up 3 months later. CONCLUSIONS: Pelvic lymph node dissection may cause postoperative chylous ascites. Paracentesis with a continuous low-pressure drainage system can be an effective conservative treatment for postoperative chylous ascites.


Subject(s)
Carcinoma, Endometrioid/surgery , Chylous Ascites/etiology , Chylous Ascites/therapy , Gynecologic Surgical Procedures/adverse effects , Postoperative Complications/therapy , Chemotherapy, Adjuvant , Drainage/methods , Female , Humans , Lymph Node Excision/adverse effects , Middle Aged , Paracentesis , Pelvis
8.
No Shinkei Geka ; 40(12): 1095-9, 2012 Dec.
Article in Japanese | MEDLINE | ID: mdl-23180747

ABSTRACT

We report a case of moyamoya disease presenting with progressive stroke during the late perinatal period, which was successfully managed by emergency caesarean section and subsequent bilateral revascularization surgeries. A 27-year-old woman at 33 weeks of pregnancy suffered from progressive monoparesis on her left hand. Magnetic resonance (MR) imaging/angiography revealed definitive moyamoya disease presenting with acute spotty cerebral infarctions on the right cerebral hemisphere. At 34 weeks of pregnancy, she was transferred to our hospital, where both neurosurgeons and obstetricians were involved in her management. She underwent emergency caesarean section on the day of admission without deterioration of her neurological status, while MRI demonstrated newly-formed spotty infarction on the left hemisphere. Then she was managed by antithrombotic therapy for 4 weeks, and then underwent right superficial temporal artery (STA)-middle cerebral artery (MCA) anastomosis, followed by left STA-MCA anastomosis one month later without complications. Postoperative course was uneventful, and MRI after surgeries showed no expansion of ischemic lesion. The MRA showed apparently patent STA-MCA bypasses bilaterally. She was discharged without complication, and her symptom significantly improved two weeks after the left revascularization surgery.


Subject(s)
Cerebral Revascularization/methods , Moyamoya Disease/surgery , Pregnancy Complications , Stroke/surgery , Adult , Female , Humans , Magnetic Resonance Angiography , Middle Cerebral Artery/surgery , Moyamoya Disease/complications , Moyamoya Disease/diagnosis , Postoperative Period , Pregnancy , Stroke/complications , Treatment Outcome
9.
Transfusion ; 43(9): 1303-8, 2003 Sep.
Article in English | MEDLINE | ID: mdl-12919434

ABSTRACT

BACKGROUND: Umbilical cord blood (CB) is being used as a source of alternative HPCs for transplantation with increasing frequency. The goal of CB banks for unrelated transplantation is to provide good quality-controlled CB units that can be transplanted for HPCs into the largest possible number of patients. STUDY DESIGN AND METHODS: Large CB samples in freezing bags wrapped with insulators and small samples in cryotubes placed into double styrene-foam boxes were cryopreserved at -85 degrees C without a rate-controlled freezing machine, followed by storage in the liquid phase of nitrogen. After thawing these cells, the viability and recovery of cells, as well as the recovery rate of HPCs such as CD34+ cells, CFU-GM, and total CFU were evaluated. RESULTS: Measurement of the freezing rate in CB bags and cryotubes demonstrated that this simple method for cryopreservation of CB cells provided optimal conditions for both large-scale and small-scale cryopreservation. Recovery of CB progenitor cells after cryopreservation was also shown to be potentially acceptable when evaluated with CD34+ cells, CFU-GM, and total CFU. These results were comparable to the method using a rate-controlled programmed freezer. CONCLUSIONS: A simple method for cryopreservation of CB cells without a rate-controlled programmed freezer could provide a sufficient-enough potential for the transplantability of HPCs after thawing.


Subject(s)
Blood Preservation/methods , Cryopreservation/instrumentation , Cryopreservation/methods , Fetal Blood/cytology , Freezing , Blood Banks/economics , Blood Preservation/economics , Cell Count , Cost Savings , Cryopreservation/economics , Humans , Reproducibility of Results , Blood Banking/methods
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