8 results on '"Boris Weizman"'
Search Results
2. A New Insight on Exophytic Serous Borderline Adnexal Tumors: Specific Sonographic Features
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Nir Kugelman, Roman Korobochka, Suraya Said-Idris, Hasan Bakry, Jacob Bejar, Zvi Leibovitz, Boris Weizman, Leila Haddad, Israel Shapiro, and Shlomi Sagie
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Ovarian Neoplasms ,Pathology ,medicine.medical_specialty ,Radiological and Ultrasound Technology ,Serous carcinoma ,business.industry ,Ultrasound ,Ovary ,medicine.disease ,Adnexal mass ,Cystadenocarcinoma, Serous ,Adnexal tumors ,Serous fluid ,Ovarian tumor ,medicine.anatomical_structure ,Adnexal Diseases ,Histological diagnosis ,medicine ,Humans ,Female ,Radiology, Nuclear Medicine and imaging ,business ,Retrospective Studies - Abstract
OBJECTIVES To characterize and compare the sonographic features of exophytic serous borderline ovarian tumors (ESBOT) with those of high-grade serous carcinoma of the ovary (HGSC). METHODS Seven patients with histological diagnosis of ESBOT diagnosed between 2011 and 2019 and 10 consecutive cases of HGSC detected during 2019, both depicting an exophytic growth pattern, were identified retrospectively. The sonographic imaging of the masses was reassessed and characterized according to the International Ovarian Tumor Analysis terms. RESULTS A unilateral irregular solid adnexal mass was demonstrated in all patients with ESBOT. The mass typically wrapped an apparently normal ovary, with a clear demarcation line depicted between them and it contained tiny cystic inclusions and calcifications. On color Doppler study of all the ESBOT cases, a unique vascular pattern could be demonstrated: an intratumoral vascular bundle originating from the ovarian vessels and supplying a rich radial blood flow to the tumor periphery. These characteristic morphological and color Doppler features could not be observed in any of the HGSC cases (P
- Published
- 2021
3. Unique Imaging Features Enabling the Prenatal Diagnosis of Developmental Venous Anomalies: A Persistent Echogenic Brain Lesion Drained by a Collecting Vein in Contrast with Normal Brain Parenchyma on MRI
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Alon Peled, Dvora Kidron, Gustavo Malinger, Boris Weizman, Karina Krajden Haratz, Liat Gindes, Tally Lerman-Sagie, Dorit Lev, Liat Ben-Sira, Zvi Leibovitz, and M. Tamarkin
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Adult ,Embryology ,medicine.medical_specialty ,Pathology ,Ultrasonography, Doppler, Transcranial ,Prenatal diagnosis ,Autopsy ,Gestational Age ,Ultrasonography, Prenatal ,030218 nuclear medicine & medical imaging ,Lesion ,03 medical and health sciences ,0302 clinical medicine ,Child Development ,Predictive Value of Tests ,Pregnancy ,Parenchyma ,medicine ,Humans ,Radiology, Nuclear Medicine and imaging ,Vein ,Parenchymal Tissue ,Central Nervous System Vascular Malformations ,Fetus ,business.industry ,Age Factors ,Obstetrics and Gynecology ,Echogenicity ,Infant ,Reproducibility of Results ,Abortion, Induced ,General Medicine ,Prognosis ,Cerebral Veins ,Magnetic Resonance Imaging ,medicine.anatomical_structure ,Pediatrics, Perinatology and Child Health ,Brain lesions ,Female ,Radiology ,medicine.symptom ,business ,030217 neurology & neurosurgery - Abstract
Objective: To describe the prenatal imaging features enabling diagnosis of developmental venous anomalies (DVA). Methods: Four fetuses with unexplained persistent echogenic parenchymal brain lesions were studied. The evaluation included dedicated neurosonography, fetal MRI, serology for intrauterine infection, screening for coagulation abnormalities, and chromosomal microarray. Postnatal neurodevelopmental follow-up or autopsy results were assessed. Results: DVA presented as very slowly growing echogenic brain lesions without cystic components, calcifications, or structural changes on otherwise normal neurosonographic scans performed at 2- to 3-week intervals. A specific Doppler feature was a collecting vein draining the echogenic parenchyma. Fetal brain MRI depicted normal anatomy on half-Fourier acquisition single-shot turbo spin-echo and diffusion-weighted imaging. The rest of the evaluation was normal. Conclusions: In cases with a persistent, parenchymal echogenic lesion without clastic or structural changes, DVA should be considered. Demonstration of a collecting vein draining the lesion and normal brain anatomy on MRI confirm the diagnosis.
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- 2016
4. Adverse effects of epidural analgesia in labor
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Etan Z. Zimmer, Aldo Glik, Ido Solt, Boris Weizman, Peter Jakobi, Zeev Weiner, and Joseph Itskovitz-Eldor
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Adult ,Time Factors ,Singleton pregnancy ,business.industry ,Previous cesarean section ,Obstetrics and Gynecology ,Gestational age ,Delivery, Obstetric ,Instrumental delivery ,Analgesia, Epidural ,Mode of delivery ,Reproductive Medicine ,Labor Stage, Second ,Pregnancy ,Anesthesia ,Analgesia, Obstetrical ,Humans ,Medicine ,Female ,Complication ,business ,Adverse effect ,reproductive and urinary physiology - Abstract
Objective: To examine the influence of epidural analgesia on labor and delivery in nulliparous and multiparous women. Design: Data were collected on 847 consecutive parturients with singleton pregnancy and vertex presentation (384 nulliparous and 463 multiparous). The obstetrical and labor characteristics including maternal age, parity, gestational age, previous cesarean section, instrumental delivery, mode and timing of analgesia, mode of delivery, indications for cesarean section or instrumental delivery were analyzed comparing patients who received epidural analgesia with women who received systemic analgesia. Results: Epidural analgesia was administered in 233 nulliparous and 141 multiparous women. A stepwise logistic regression analysis revealed that epidural analgesia independently affected the rate of non-spontaneous delivery and the duration of the second stage of labor in nulliparous (P=0.0017 and P=0.0036, respectively) and multiparous (P=0.001 and P=0.0081, respectively) women. Epidural analgesia independently affected the duration of labor only in nulliparous women (P=0.0001). Conclusion: Women should be informed that prolongation of labor and increase in nonspontaneous deliveries should be expected when choosing epidural analgesia in labor.
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- 2000
5. The nuchal translucency examination leading to early diagnosis of structural fetal anomalies
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Israel Goldstein, Zeev Weiner, Khatib Nizar, and Boris Weizman
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Fetus ,medicine.medical_specialty ,Pregnancy ,medicine.diagnostic_test ,business.industry ,Obstetrics ,Urinary system ,Ultrasound ,Obstetrics and Gynecology ,Gestational Age ,medicine.disease ,Pediatrics, Perinatology and Child Health ,medicine ,Amniocentesis ,Gestation ,Atrioventricular canal ,Humans ,Sampling (medicine) ,Female ,business ,Nuchal Translucency Measurement - Abstract
Objective To evaluate the ability to diagnose structural fetal anomalies during or soon after an extended nuchal translucency (NT) examination. Methods The study population included all women who had a routine NT examination in the ultrasound division of one of three centers. Also included in the study were women referred to these centers following an abnormal NT examination. The sonographers were instructed to pay attention to fetal anomalies while performing the NT examination. Each examination was initially attempted transabdominally. Failure to obtain adequate views transabdominally was an indication for a transvaginal examination. When a structural fetal anomaly was detected or suspected, a full fetal anomaly scan was performed. When a diagnosis could not be established, fetal anatomy scan was repeated after 14 weeks of gestation. Fetal cardiac scanning was performed transvaginally, immediately or within 3 days after an increased NT was observed. When fetal anomalies were diagnosed the patients were informed about the possibilities of terminating the pregnancy or continuing the work-up and follow-up. Overall, ascertainment of fetal outcome was available in 85% of the study population. Results We performed 4467 NT examinations during the study period and additional 123 fetal cardiac scanning following an abnormal NT examination. Overall, we performed 365 fetal cardiac scanning between 11 and 14 weeks of gestation. The fetal anomalies detected included the following: three skeletal anomalies, seven brain anomalies, four urinary system anomalies, four abdominal anomalies, two facial anomalies, and 13 cardiac anomalies. Six of the 13 cardiac anomalies were found in the atrioventricular canal. One third of the patients (11/33) elected to discontinue the pregnancy a short time after the detection of the congenital anomaly (until 14 weeks of gestation) and half of the patients (16\33) asked for termination of pregnancy later. More than 60% of the patients (20/33) with congenital anomalies detected following the NT examination refused to have chorionic villous sampling (CVS) or amniocentesis. Conclusion The opportunity to scan the fetal anatomy in the early stages of pregnancy, when the NT examination is performed, justifies the approach of extended NT examination.
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- 2013
6. Sonographic evaluation of the superior sinus sagittalis
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Israel Goldstein, Boris Weizman, Zeev Wiener, and Ada Tamir
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Embryology ,Fetus ,business.industry ,Obstetrics and Gynecology ,Gestational age ,Prenatal diagnosis ,General Medicine ,Anatomy ,Ultrasonography, Prenatal ,SSS ,Fetal Development ,Frontal bone ,Pregnancy ,Coronal plane ,embryonic structures ,Pediatrics, Perinatology and Child Health ,Gestation ,Medicine ,Humans ,Radiology, Nuclear Medicine and imaging ,Fetal head ,Female ,Sagittal Sinus Thrombosis ,business ,Superior Sagittal Sinus - Abstract
Objective: The aim of this study was to characterize the normal ultrasonographic growth of the fetal superior sinus sagittalis (SSS) throughout gestation. Patients and Methods: In a prospective cross-sectional study, measurements of the fetal sinus sagittalis were obtained in patients undergoing elective fetal anatomical surveys or fetal growth scan at between 16.6 and 34.7 weeks of gestation. Special attention was given to the SSS of the fetal brain. On the coronal plane, the SSS may be easily identified immediately below the frontal bone, and anterior to the fetal head parenchyma. Results: 206 fetuses were scanned. A regression line of the SSS was created throughout gestation and a first-degree correlation was found between gestational age (GA) and the SSS height (r = 0.418; p < 0.0001; SSS = -0.015 + 0.0178 × GA). Normal values were established for different gestational weeks. Conclusion: We provide ultrasonographic dimensions of the fetal SSS across pregnancy. This data potentially allows for prenatal diagnosis of abnormal appearance of the SSS.
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- 2011
7. Fetal cardiac scanning performed immediately following an abnormal nuchal translucency examination
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Ron Beloosesky, Boris Weizman, Israel Goldstein, Allan Bombard, and Zeev Weiner
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Adult ,medicine.medical_specialty ,Adolescent ,Sensitivity and Specificity ,Ultrasonography, Prenatal ,Young Adult ,Fetal Heart ,Pregnancy ,Nuchal Translucency Measurement ,medicine ,Humans ,Sampling (medicine) ,Neonatology ,Young adult ,Genetics (clinical) ,Fetus ,medicine.diagnostic_test ,Obstetrics ,business.industry ,Obstetrics and Gynecology ,Middle Aged ,medicine.disease ,Pregnancy Trimester, First ,Echocardiography ,embryonic structures ,Gestation ,Feasibility Studies ,Female ,business ,Fetal echocardiography - Abstract
Objective To study the implications of early fetal cardiac scanning immediately following an abnormal nuchal translucency (NT) examination. Methods Fetal cardiac scanning was performed immediately after an increased NT was observed. Scans were performed transvaginally at 11 to 14 weeks. Fetal echocardiography was repeated between 14 and 24 weeks in continuing pregnancies, or when the cardiac scanning appeared normal at 11 to 14 weeks. Results We performed 2513 NT examinations. An abnormal NT was observed in 135 (5.4%) patients. In addition, 65 patients with an abnormal NT were referred to us for fetal cardiac scanning from other offices. Overall, we performed 200 fetal cardiac scans between 11.2 and 13.5 weeks for an abnormal NT examination. Twelve major fetal cardiac anomalies were diagnosed between 12 and 13.5 weeks. Seven patients (58%) terminated pregnancy between 12 and 14 weeks without performing chorionic villous sampling (CVS). Five patients asked for chromosomal analysis before deciding about their pregnancy. Fetal cardiac anomalies were suspected in six additional cases, but only one of them was diagnosed. Another five minor and one major fetal cardiac anomaly were suspected at 11 to 14 weeks but diagnosed later on fetal echocardiography. Conclusion Major fetal cardiac anomalies can be detected immediately following an abnormal NT examination and be useful for the patients' decisions about the management of their pregnancy. Copyright © 2008 John Wiley & Sons, Ltd.
- Published
- 2008
8. 163: Fetal cardiac scanning performed immediately following an abnormal NT examination
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Boris Weizman, Allan Bombard, Israel Goldstein, Ron Beloosesky, and Zeev Weiner
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Fetus ,Pathology ,medicine.medical_specialty ,business.industry ,medicine ,Obstetrics and Gynecology ,business - Published
- 2007
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