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胎儿泌尿生殖系统异常的超声诊断及围产期管理

Ultrasound diagnosis and perinatal management of fetal genito-urinary abnormalities.

作者信息

Kurjak A, Latin V, Mandruzzato G, D'Addario V, Rajhvajn B

出版信息

J Perinat Med. 1984;12(6):291-312. doi: 10.1515/jpme.1984.12.6.291.

Abstract

Approximately 50% of fetal abdominal masses originate in the urinary system and those recognizable ultrasonically include renal dysplasia, renal agenesis and obstruction of the lower excretory channels. Fetal renal anomalies may be discovered co-incidentally during the course of sonographic evaluation of uterine size-dates discrepancy, because they are commonly associated with fetal growth retardation and/or oligohydramnios, or during a planned sonographic follow-up of pregnancies in patients who are at risk of recurrence of such anomalies. The sonographic demonstration of renal anomalies under these circumstances may allow for elective termination of pregnancy, may modify the obstetric management and/or facilitate pediatric and surgical care of the newborn. In the collaboration study at three ultrasonic centers there were 81 cases of genito-urinary tract anomalies detected antenatally in a five years period. Among the detected anomalies there were 30 hydronephrotic fetuses, 12 with multicystic disease, 15 with Potter's syndrome, 10 with polycystic kidney, 9 with Prune Belly syndrome, 4 with isolated renal cysts and 1 with an ovarian cyst. Perinatal management of the fetus with urinary tract abnormalities greatly depends on the accuracy of the diagnosis. It would be justifiable to suggest that an inexperienced observer should not make the final diagnosis. He could be of great help, if one kept a high index of suspicion in patients with a significant family history of oligohydramnios and of unexplained abnormal cystic structures in the fetal abdomen and seek the help of a special referral center where experience in related cases is concentrated. Once an accurate diagnosis is made, various alternatives are open to the obstetrician. This is primarily dependent upon the type and degree of the abnormality. Unilateral multicystic kidney and hydronephrosis due to obstruction above the level of the urethra appear to be compatible with extrauterine life and should be approached accordingly. If there is massive enlargement of the fetal abdomen, elective cesarean delivery should be considered to prevent the dystocia which may occur with vaginal delivery and to prevent further damage of these vital organs. If bilateral renal agenesis, bilateral multicystic kidneys, or bilateral infantile polycystic kidneys are demonstrated early in gestation, the obstetrician and parents may choose to terminate the pregnancy because these conditions are not compatible with extrauterine life.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

约50%的胎儿腹部肿块起源于泌尿系统,超声可识别的包括肾发育不全、肾缺如及下尿路梗阻。胎儿肾异常可能在超声评估子宫大小与孕周不符的过程中偶然发现,因为它们常与胎儿生长受限和/或羊水过少相关,或者在有此类异常复发风险的患者进行计划中的超声随访时发现。在这些情况下,超声显示肾异常可能允许选择性终止妊娠,可能改变产科管理和/或促进新生儿的儿科及外科护理。在三个超声中心的合作研究中,五年期间共产前检测出81例泌尿生殖道异常。在检测出的异常中,有30例胎儿肾积水,12例多囊性疾病,15例波特综合征,10例多囊肾,9例梅干腹综合征,4例孤立性肾囊肿,1例卵巢囊肿。泌尿系统异常胎儿的围产期管理很大程度上取决于诊断的准确性。有理由建议,没有经验的观察者不应做出最终诊断。如果对羊水过少家族史明显且胎儿腹部有不明原因异常囊性结构的患者保持高度怀疑,并寻求相关病例经验集中的特殊转诊中心的帮助,那么没有经验的观察者也可能会有很大帮助。一旦做出准确诊断,产科医生有多种选择。这主要取决于异常的类型和程度。单侧多囊肾及尿道以上梗阻所致肾积水似乎与宫外生活相容,应相应处理。如果胎儿腹部大量增大,应考虑选择性剖宫产,以防止阴道分娩可能出现的难产,并防止这些重要器官进一步受损。如果在妊娠早期发现双侧肾缺如、双侧多囊肾或双侧婴儿型多囊肾,产科医生和父母可能会选择终止妊娠,因为这些情况与宫外生活不相容。(摘要截选至400词)

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