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1. |
Abnormal Biochemical Serum Screening versus 2nd-Trimester Ultrasound-Detected Minor Anomalies as Predictors of Aneuploidy in Low-Risk Patients |
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Fetal Diagnosis and Therapy,
Volume 11,
Issue 5,
1996,
Page 301-305
Arie Drugan,
Avikai Reichler,
Moshe Bronstein,
Mark P. Johnson,
Robert J. Sokol,
Mark I. Evans,
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摘要:
Objective: To compare the yield of multiple-marker biochemical screening with that of minor fetal anomalies observed on ultrasound for detection of aneuploidy in low-risk patients. Methods: The results of 1,073 amniocenteses performed because of abnormal biochemical screening tests were compared against 197 amniocenteses performed for minor anomalies as detected on level II ultrasound at 15–22 weeks of gestation. Results: False-positive results were observed in about 7% of serum screening patients and in 1.7% of the ultrasound cases. Chromosomally abnormal fetuses were detected in 2% of the amniocenteses performed because of abnormal serum screening and in 2.5% of the cases with ultrasound-defined minor anomalies. Conclusions: Both methods identify patients at risk for abnormal karyotypes. Although the evaluation of serum biochemical markers yielded more false-positive results, it is more suitable than ultrasound for mass population screenin
ISSN:1015-3837
DOI:10.1159/000264328
出版商:S. Karger AG
年代:1996
数据来源: Karger
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2. |
In utero Fetal Urine Analysis and Renal Histology Correlate with the Outcome in Fetal Obstructive Uropathies |
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Fetal Diagnosis and Therapy,
Volume 11,
Issue 5,
1996,
Page 306-312
Faisal Qureshi,
Suzanne M. Jacques,
Brian Seifman,
Ruben Quintero,
Mark I. Evans,
Craig Smith,
Mark P. Johnson,
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摘要:
We evaluated 8 second-trimester fetuses who had undergone termination because of obstructive uropathies and correlated the renal histopathology with fetal urine biochemical prognostic parameters. Prenatal evaluation included serial vesicocentesis, karyotyping, and sonography. According to the urinary biochemical parameters, 3 fetuses were classified to be in the good prognostic category, 2 in the borderline prognostic category, and 3 in the poor prognostic category. The kidneys were evaluated both grossly and microscopically for hydronephrosis, pelvicaliceal dilatation, cystic changes and fibrosis. Fetuses in the poor prognostic category had severely damaged renal architecture, microcysts, macrocysts, and extensive fibrosis. Fetuses in the good prognostic category had minimal histopathologic changes with preservation of the architecture. Fetuses in the borderline category showed a moderate degree of renal damage but with focally preserved architecture. We conclude (1) that there is a direct correlation between elevation in urinary electrolytes and proteins and extent of underlying renal histopathological damage and (2) that appropriate detailed prenatal evaluation of the renal function can identify fetuses who could potentially benefit from in utero therapy.
ISSN:1015-3837
DOI:10.1159/000264329
出版商:S. Karger AG
年代:1996
数据来源: Karger
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3. |
Double Shunt in a Case of Fetal Low-Level Obstructive Uropathy |
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Fetal Diagnosis and Therapy,
Volume 11,
Issue 5,
1996,
Page 313-317
Giuseppe Noia,
Marco De Santis,
Carmen Mastromarino,
Carmen Trivellini,
Domenico Romano,
Alessandro Caruso,
Salvatore Mancuso,
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摘要:
This report describes a pregnant woman at 22 weeks of gestation examined for fetal bilateral dilated renal pelvis and oligohydramnios. Ultrasound evaluation confirmed the diagnosis of low-level obstructive uropathy. At 26 weeks of gestation, the increase in hydronephrosis prompted us to introduce a vesicoamnionic shunt. Because of unusual intraperitoneal dislocation of the shunt and an increase in ascites and hydronephrosis, we had to insert a peritoneoamnionic shunt at 30 weeks of gestation. The patient underwent cesarean section at 31 weeks for obstetric complications. The infant, at 15 months of age, showed mild renal failure.
ISSN:1015-3837
DOI:10.1159/000264331
出版商:S. Karger AG
年代:1996
数据来源: Karger
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4. |
Cytokine Stimulation of Human Fetal Hematopoietic Cells |
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Fetal Diagnosis and Therapy,
Volume 11,
Issue 5,
1996,
Page 318-325
Sverker Ek,
Magnus Westgren,
Lola Markling,
Anders Kjeldgaard,
Olle Ringdén,
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摘要:
The effects of interleukins 3 and 6, stem cell factor, and granulocyte-macrophage colony-stimulating factor on human fetal hematopoietic, bone marrow, and cord blood cells were studied on the basis of the colony-forming capacity. Fetal hematopoietic cells from 28 elective abortions, three bone marrow samples, and three cord blond samples were incubated with cytokines and investigated for the presence of BFU-E (burstforming units – erythroid), CFU-GM (colony-forming units – granulocytes, macrophages), and CFU-GEMM (colony-forming units – granulocytes, erythrocytes, macrophages, megakaryocytes). Single and combined cytokines and preincubation versus adding cytokines in culture were investigated. Interleukin-6 alone had the most pronounced effect on BFU-E formation. All four cytokines in combination yielded the highest scores for CFU-GM (p < 0.05) and CFU-GEMM (p < 0.05), whereas BFU-E was not enhanced. The mode of cytokine exposure was not a determinant of colony form
ISSN:1015-3837
DOI:10.1159/000264333
出版商:S. Karger AG
年代:1996
数据来源: Karger
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5. |
Colony Formation of Human Fetal CD34+ Hematopoietic Cells |
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Fetal Diagnosis and Therapy,
Volume 11,
Issue 5,
1996,
Page 326-334
Sverker Ek,
Lola Markling,
Olle Ringdén,
Anders Kjeldgaard,
Magnus Westgren,
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摘要:
Manipulations to enhance engraftment of donated cells may be advantageous in transplantation of fetal hematopoietic cells (FHC). By assessing the formation of colonies, CD34+ enrichment was evaluated with and without cytokine stimulation (interleukins 3 and 6, stem cell factor, granulocyte-macrophage colony-stimulating factor). Cord blood cells and bone marrow cells served as controls. In FHC, cytokine stimulation and CD34+ enrichment always enhanced the formation of CFU-GM (colony-forming units – granulocytes, macrophages) and CFU-GEMM (colony-forming units – granulocytes, erythroid cells, macrophages, megakaryocytes). However, BFU-E (burst-forming units – erythroid cells) in FHC remained unchanged after cytokine stimulation and CD34+ enrichment. In FHC, the addition of cytokines and the enrichment of CD34+ cells usually contributed equally to enhance CFU-GM and CFU-GEMM colony formation. CD34-negative FHC produced the same number or more BFU-E and half the number of CFU-GM and CFU-GEMM as compared with crude cells. This CD34-negative cell population also responded to cytokine stimulation. Such findings may indicate that purification of CD34+ cells is not meaningful in fetal transpla
ISSN:1015-3837
DOI:10.1159/000264335
出版商:S. Karger AG
年代:1996
数据来源: Karger
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6. |
Use of Three-Dimensional Ultrasound to Establish the Prenatal Diagnosis of Fryns Syndrome |
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Fetal Diagnosis and Therapy,
Volume 11,
Issue 5,
1996,
Page 335-340
Didier Van Wymersch,
Romain Favre,
Bernard Gasser,
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摘要:
Three-dimensional (3D) imaging permits surface reconstructions that allow a better view of the appearance of organs. We report a case of a fetus with cystic hygroma diagnosed at 11 weeks of gestation, associated with a diaphragmatic hernia. With the 3D reconstruction, we examined the fetal face much more easily, which presented facial dysmorphology, retrognathia, macrostomia and a broad nasal bridge. The conjunctions of these pathological features and a normal karyotype allowed to establish a prenatal diagnosis of Fryns syndrome, confirmed by autopsy.
ISSN:1015-3837
DOI:10.1159/000264336
出版商:S. Karger AG
年代:1996
数据来源: Karger
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7. |
Indomethacin and Fetal Ductus arteriosus: Complete Closure after Cessation of Prolonged Therapeutic Course |
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Fetal Diagnosis and Therapy,
Volume 11,
Issue 5,
1996,
Page 341-344
Yehuda Ben-David,
Mordechai Hallak,
Avi Rotschild,
Yoram Sorokin,
Ron Auslender,
Haim Abramovici,
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摘要:
Indomethacin is a very effective tocolytic agent. However, concern about its possible constrictive effect on fetal ductus arteriosus has limited the use of this medication in pregnancy. A 29-year-old woman was treated with indomethacin at 27 weeks of gestation for preterm labor and polyhydramnios. She received a dose of 75 mg/day for 5 weeks. At 35 weeks of gestation, she had a cesarean delivery due to fetal distress, and a hydropic baby was delivered. The infant died shortly after. Nonimmune hydrops fetalis and closed ductus arteriosus were the only pathological findings at autopsy. In utero, irreversible, complete closure of the ductus arteriosus is very rare. In the case presented, prolonged use of indomethacin during pregnancy was associated with complete closure of the ductus arteriosus that developed most probably after discontinuation of therapy. This case emphasizes the need for frequent fetal echocardiography examinations during as well as after maternal indomethacin treatment.
ISSN:1015-3837
DOI:10.1159/000264338
出版商:S. Karger AG
年代:1996
数据来源: Karger
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8. |
Complete Resolution of CMV-Associated Acute Hydramnios by Single Large Volume Reduction Amniocentesis and Maternal Indomethacin |
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Fetal Diagnosis and Therapy,
Volume 11,
Issue 5,
1996,
Page 345-347
Nabeel Bondagji,
Frank A. Manning,
Jocelyne Martel,
Christopher R. Harman,
Ian Morrison,
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摘要:
Acute hydramnios is a rare complication of pregnancy, usually of idiopathic etiology and associated with a very poor perinatal prognosis. In this single case report, acute hydramnios at 21 weeks’ gestation, associated with fetal CMV infection, was treated by a single large volume reduction amniocentesis combined with maternal indomethacin therapy and result in delivery of a near term survivo
ISSN:1015-3837
DOI:10.1159/000264339
出版商:S. Karger AG
年代:1996
数据来源: Karger
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9. |
Repair Kinetics of Amnion Cells after Microsurgical Injury |
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Fetal Diagnosis and Therapy,
Volume 11,
Issue 5,
1996,
Page 348-356
Ruben A. Quintero,
Carlos A. Carreño,
Frank Yelian,
Mark I. Evans,
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摘要:
Objective: There is a paucity of data regarding healing of fetal membranes. We assessed the repairing ability of a microsurgically-injured monolayer of amnion-derived cells compared to an endothelial cell line. Materials and Methods: Amnion-derived cells (FL cells) were grown to confluence in 10% fetal calf serum (FCS). A microsurgical incision was performed under an inverted microscope. The area of each incision was measured at times 0, 6, 12 and 24 h using MCID M4 image analysis software. The experiments were repeated using 1% FCS. The observations were also made replacing the media at 6 and 12 h. Umbilical-cord-derived endothelial cells were used for comparison. The rate of repair of the incision was measured using three methods: (a) absolute closure rate (ACR): (A0 –– A1)/T, where A0 is the original incisional area, and A1 is the new area at interval T; (b) relative percentage rate (RPR): (A0 –– A1)/A0/T × 100, and (c) healing rate (HR): (A0 ––A1)/A0 × 100. Results: Amnion cells were capable of repairing the microsurgical defect. The ACR decreased over time, and was higher with larger defects. A lower concentration of FCS nor the addition of fresh media altered the repair process significantly. Endothelial cells were significantly faster than amnion cells or amnion-supplemented cells with endothelial media. The RPR remained relatively constant for all groups, suggesting Gompertzian kinetics. Conclusions: Amnion cells are capable of repairing a surgical defect at a relatively constant percent rate, but are slower than an endothelial cell line. The decreased rate of closure over time may be due to relative contact inhibition. Further studies will concentrate on the molecular and cellular mechanisms involved in
ISSN:1015-3837
DOI:10.1159/000264340
出版商:S. Karger AG
年代:1996
数据来源: Karger
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10. |
Large Chorioangioma Associated with Hydrops fetalis: Prenatal Diagnosis and Management |
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Fetal Diagnosis and Therapy,
Volume 11,
Issue 5,
1996,
Page 357-360
Claude D’Ercole,
Ludovic Cravello,
Leon Boubli,
Corinne Labif,
Véronique Millet,
Alain Potier,
Bernard Blanc,
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摘要:
A large chorioangioma located at the insertion area of the umbilical cord was diagnosed at 19 weeks of gestation by ultrasound and color Doppler ultrasound. This chorioangioma led to a progressively appearing hydrops fetalis and to fetal distress. The infant presented at birth with edemas and ascites associated with severe hemolytic anemia and thrombocytopenia.
ISSN:1015-3837
DOI:10.1159/000264341
出版商:S. Karger AG
年代:1996
数据来源: Karger
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