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对有发生髋关节发育不良的高风险儿进行髋部超声扫描筛查
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作者 Lowry C.A. Donoghue V.B. +1 位作者 murphy j.f. 郭战宏 《世界核心医学期刊文摘(儿科学分册)》 2005年第10期15-16,共2页
Background: Clinical examination, while useful, has been shown to be insuffici ent as the sole screening method in infants. Ultrasound examination at 8 weeks i n high risk infants is an integral part of the screening ... Background: Clinical examination, while useful, has been shown to be insuffici ent as the sole screening method in infants. Ultrasound examination at 8 weeks i n high risk infants is an integral part of the screening process in some units. Aims: To snow the efficiency of hip sonography in detection of developmental dys plasia of the hips in those without clinically dislocated hips. Methods: All inf ants born at the National Maternity Hospital between January 1994 and December 2 001 were included. All those with clinically dislocated hips were treated by a P avlik harness and referred for follow up to a paediatric orthopaedic surgeon. An 8 week hip ultrasound scan was performed for those infants with stable hips on examination but who met the following criteria: (1) a first degree relative with congenital dislocation of hips; (2) breech presentation at birth; and (3) a per sistent “click”at birth in an otherwise stable hip. Results: During the period of study a total of 52 893 infants were born in the National Maternity Hospital . Based on the criteria above, 5485 hip ultrasound scans were performed. Of thos e scanned, 18 (0.33%)were found to have dislocated hips and 153 (2.78%)-to ha ve dysplasic hips. The 18 infants with dislocation were treated with Pavlik harn ess; the remaining 153 were followed up by serial ultrasound examinations but di d not require active intervention. Conclusions: Among the population of infants at increased risk of developmental dysplasia of the hip, the hip screening progr amme identified 18 cases among 5485 infants; a rate of 3.2 per 1000. Hip sonogra phy is therefore worthwhile. 展开更多
关键词 髋关节发育不良 髋部 筛查方法 髋关节脱位 超声扫描 超声检查 妇产科医院 超声筛查 臀位 整形外科医师
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卵巢外类固醇细胞肿瘤是男性化罕见原因
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作者 Smith D. Crotty T.B. +2 位作者 murphy j.f. T.J.McKenna 张旸 《世界核心医学期刊文摘(妇产科学分册)》 2006年第4期35-35,共1页
Objective: To report the case of a female who presented in childhood with symptoms and signs of hyperandrogenism secondary to an extraovarian steroid cell tumor. Design: Case report. Setting: Endocrine investigation u... Objective: To report the case of a female who presented in childhood with symptoms and signs of hyperandrogenism secondary to an extraovarian steroid cell tumor. Design: Case report. Setting: Endocrine investigation unit of a university teaching hospital. Patient(s): An 11-year-old female presented with symptoms and signs of hyperandrogenism. Intervention(s): Ultrasonography, MRI imaging, bilateral adrenal and ovarian venous sampling, laparoscopy, and laparotomy. Main Outcome Measure(s): Ultrasonography, laboratory tests. Result(s): Hyperandrogenism was due to an extraovarian steroid cell tumor located in the broad ligament. The tumor was successfully removed at laparotomy with biochemical and clinical resolution of the hyperandrogenism. Conclusion(s): Extraovarian steroid cell tumor is a rare cause of hyperandrogenism. 展开更多
关键词 阔韧带 双侧肾上腺 腹腔镜手术 大学教学医院 女性病例 临床症状 生化指标
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