Wang Zhe,He Qiuming,Wang Haiyu,et al.Evaluation and treatment of prenatal persistent cloaca: two case reports and literature review[J].Journal of Clinical Pediatric Surgery,2020,19(10):884-890.[doi:10.3969/j.issn.1671-6353.2020.10.005]
产前诊断泄殖腔畸形的围生期评估及治疗——附2例报道及文献回顾
- Title:
- Evaluation and treatment of prenatal persistent cloaca: two case reports and literature review
- 分类号:
- R726.1;R726.2;R657.1;R714.5
- 摘要:
- 目的 分析总结泄殖腔畸形的产前诊断、围生期评估及治疗经验。方法 收集2017年1月至2019年12月广州市妇女儿童医疗中心收治的2例产前诊断为泄殖腔畸形并完成根治手术患儿的临床资料,对病例特点进行讨论分析,并通过PubMed、万方数据库进行文献检索,总结泄殖腔畸形产前诊断及新生儿期序贯治疗的经验。病例1产前初始异常表现为肠管扩张、肠腔内回声增强,孕晚期发现外生殖器外观异常及双侧阴道少量积液,诊断为泄殖腔畸形,出生后先后行横结肠造瘘口、根治手术及造瘘口闭合术。病例2产前初始异常表现为大量阴道积液,左侧肾积水伴输尿管全程扩张,诊断为泄殖腔畸形,出生后先后行横结肠造瘘口、阴道造瘘口及膀胱造瘘口术,进而行根治手术及造瘘口闭合术。2例患儿均预后良好。结果 检索文献共38篇,其中中文文献1篇,英文文献37篇。回顾资料完整的13例产前发现异常的泄殖腔畸形胎儿的文献,发现阴道积液是最常见的产前征象,3例因胎儿期尿潴留需要产前干预,仅1例因胎儿严重畸形建议引产,9例患儿生后存活。结论 泄殖腔畸形的产前诊断虽然有长足进步但仍然存在一定困难,胎儿与新生儿"无缝衔接"的序贯化治疗将成为积极改变泄殖腔畸形治疗及预后的一种新模式。
- Abstract:
- Objective To review the prenatal diagnosis and treatments of 2 girls of persistent cloaca malformation and summarize the experiences of prenatal diagnosis,evaluations and neonatal treatments.Methods From January 2017 to December 2019,two girls with cloacal malformation underwent radical surgery.Their clinical characteristics were analyzed by retrieving their medical records and imaging data.The initial abnormalities of case 1 were intestinal dilation and enhanced echo of meconium.Abnormal appearance of external genitalia and minimal bilateral vaginal fluid were found during the third trimester.Cloaca malformation was diagnosed.Transverse colonostomy,radical surgery and stoma closure were performed in sequence.The prenatal abnormality of case 2 was massive hydrocolpos and left hydronephrosis accompanied by ureteral dilatation.She was diagnosed as cloaca malformation.Transverse colostomy,vaginostomy and cystostomy were performed successively postnatally and then radical surgery and stoma closure completed.Both girls had a good prognosis.Results A total of 38 papers were retrieved,including 1 in Chinese and 37 in English.Complete reports were reviewed for 13 fetuses with cloaca deformities before delivery.And hydrocolpos was the most common prenatal sign.Three fetuses required prenatal interventions due to urinary retention.And 9 fetuses survived after birth.Conclusion Although prenatal diagnosis of cloaca malformations has made great advances,there are still some difficulties.The sequential treatment of "seamless integration" between fetus and newborn shall become a new model for actively changing the treatments and prognosis of cloaca malformations.
参考文献/References:
1 Jaramillo D,Lebowitz RL,Hendren WH.The cloacal malformation:radiologic findings and imaging recommendations[J].Radiology,1990,177(2):441-448.DOI:10.1148/radiology.177.2.2217782.
2 Williams DH 4th,Fitchev P,Policarpio-Nicolas ML,et al.Urorectal septum malformation sequence[J].Urology,2005,66(3):657.DOI:10.1016/j.urology.2005.03.003.
3 Bischoff A.The surgical treatment of cloaca[J].Semin Pediatr Surg,2016,25(2):102-107.DOI:10.1053/j.sempedsurg.2015.11.009.
4 Levitt MA,Pe?a A.Cloacal malformations:lessons learned from 490 cases[J].Semin Pediatr Surg,2010,19(2):128-138.DOI:10.1053/j.sempedsurg.2009.11.012.
5 Levitt MA,Pe?a A.Pitfalls in the management of newborn cloacas[J].Pediatr Surg Int,2005,21(4):264-269.DOI:10.1007/s00383-005-1380-2.
6 张小康,黄金狮,陶强,等.一穴肛2例报告并文献复习[J].临床小儿外科杂志,2013,12(2):159-160.DOI:10.3969/j.issn.1671-6353.2013.02.026. Zhang XK,Huang JS,Tao Q,et al.A report of 2 cases of cloaca and literature review[J].J Clin Ped Sur,2013,12(2):159-160.DOI:10.3969/j.issn.1671-6353.2013.02.026.
7 Salomon LJ,Alfirevic Z,Berghella V,et al.Practice guidelines for performance of the routine mid-trimester fetal ultrasound scan[J].Ultrasound Obstet Gynecol,2011,37(1):116-126.DOI:10.1002/uog.8831.
8 许云燕,李雪蕾,穆仲平.泄殖腔畸形的产前超声诊断和文献复习[J].中国超声医学杂志,2017,33(12):1138-1140.DOI:10.3969/j.issn.1002-0101.2017.12.032. Xu YY,Li XL,Mu ZP.Prenatal sonographic findings and review of cloacal malformation[J].Chinese J Ultrasound Med,2017,33 (12):1138-1140.DOI:10.3969/j.issn.1002-0101.2017.12.032.
9 Kubota M,Osuga Y,Kato K,et al.Treatment guidelines for persistent cloaca,cloacal exstrophy and Mayer-Rokitansky-Kuster-Hauser syndrome for the appropriate transitional care of patients[J].Surg Today,2019,49(12):985-1002.DOI:10.1007/s00595-019-01810-z.
10 Chitrit Y,Vuillard E,Khung S,et al.Cloaca in discordant monoamniotic twins:prenatal diagnosis and consequence for fetal lung development[J].AJP Rep,2014,4(1):33-36.DOI:10.1055/s-0034-1370351.
11 Sahinoglu Z,Cerrah Celayir A,Resit Asoglu M,et al.Diagnostic difficulties in a case of persistent cloaca with hydrocolpos[J].J Neonatal Surg,2012,1(4):55.
12 Nigam A,Kumar M,Gulati S.Fetal ascites and hydrometrocolpos due to persistent urogenital sinus and cloaca:a rare congenital anomaly and review of literature[J].BMJ Case Rep,2014, 2014:bcr2013202231.DOI:10.1136/bcr-2013-202231.
13 Kanda T,Iizuka T,Yamazaki R,et al.Giant fetal hydrometrocolpos associated with cloacal anomaly causing postnatal respiratory distress[J].J Obstet Gynaecol Res,2017,43(11):1769-1772.DOI:10.1111/jog.13433.
14 Arena S,Russo T,Perrone P,et al.Operative cystoscopy in the neonatal period[J].Pediatr Med Chir,2016,38(3):136.DOI:10.4081/pmc.2016.136.
15 Chen CP,Chang TY,Hsu CY,et al.Persistent cloaca presenting with a perineal cyst:Prenatal ultrasound and magnetic resonance imaging findings[J].J Chin Med Assoc,2012,75(4):190-193.DOI:10.1016/j.jcma.2012.02.007.
16 Chen CP,Liu YP,Chang TY,et al,Prenatal diagnosis of persistent cloaca with hydrometrocolpos and ascites by magnetic resonance imaging in one fetus of a dizygotic twin pregnancy[J].Taiwan J Obstet Gynecol,2010,49(3):385-386.DOI:10.1016/S1028-4559(10)60082-4.
17 Warne S,Chitty LS,Wilcox DT.Prenatal diagnosis of cloacal anomalies[J].BJU International,2002,89(1):78-81.DOI:10.1046/j.1464-410X.2002.02556.x.
18 Bischoff A,Levitt MA,Lim FY,et al.Prenatal diagnosis of cloacal malformations[J].Pediatr Surg Int,2010,26(11):1071-1075.DOI:10.1007/s00383-010-2685-3.
19 Livingston JC,Elicevik M,Breech L,et al.Persistent cloaca:a 10-year review of prenatal diagnosis[J].J Ultrasound Med,2012,31(3):403-407.DOI:10.7863/jum.2012.31.3.403.
20 Cerrah Celayir A,Kurt G,Sahin C,et al.Spectrum of etiologies causing hydrometrocolpos[J].J Neonatal Surg,2013,2(1):5.
21 Diana W.Bianchi TMC,Mary E.et al.Fetology:Diagnosis and Management of the Fetal Patient[M].2nd ed.New York:McGraw-Hill Education,2000:482-490.
22 Zangheri G,Andreani M,Ciriello E,et al.Fetal intra-abdominal calcifications from meconium peritonitis:sonographic predictors of postnatal surgery[J].Prenat Diagn,2007,27(10):960-963.DOI:10.1002/pd.1812.
23 Staboulidou I,Schauer J,Rau GA,et al.Antenatal ultrasonographic appearance of isolated fetal ascites.A case report of sinus urogenitalis[J].Fetal Diagn Ther,2006,21(6):501-505.DOI:10.1159/000095661.
24 Uttarwar AM,Joshi RS,Ramji J,et al.Persistent cloaca associated with unilateral lung agenesis-a rare presentation[J].J Neonatal Surg,2014,3(2):22.
25 Harrison MR,Nakayama DK,Noall R,et al.Correction of congenital hydronephrosis in utero Ⅱ.Decompression reverses the effects of obstruction on the fetal lung and urinary tract[J].J Pediatr Surg,1982,17(6):965-974.DOI:10.1016/s0022-3468(82)80476-4.
26 郑珊,张培,董岿然,等.先天性肛门直肠畸形肛门成形术后再手术的临床分析[J].中华小儿外科杂志,2012,33(4):296-299.DOI:10.3760/cma.j.issn.0253-3006.2012.04.014. Zheng S,Zhang P,Dong KR,et al.Retrospective study of reoperation for congenital anorectal malformation[J].Chin J Ped Surg,2012,33(4):296-299.DOI:10.3760/cma.j.issn.0253-3006.2012.04.014.
27 Cho MJ,Kim TH,Kim DY,et al.Clinical experience with persistent cloaca[J].J Korean Surg Soc,2011,80(6):431-436.DOI:10.4174/jkss.2011.80.6.431.
28 李胜利,张军,明安晓,等.先天性球形结肠20例诊治体会[J].临床小儿外科杂志,2012,11(1):36-38.DOI:10.3969/j.issn.1671-6353.2012.01.016. Li SL,Zhang J,Ming AX,et al.Diagnosis and treatment of 20 cases of congenital spherical colon[J].J Clin Ped Sur,2012,11(1):36-38.DOI:10.3969/j.issn.1671-6353.2012.01.016.
29 Vander Brink BA,Reddy PP.Early urologic considerations in patients with persistent cloaca[J].Semin Pediatr Surg,2016,25(2):82-89.DOI:10.1053/j.empedsurg.2015.11.005.
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备注/Memo
收稿日期:2020-03-10。
通讯作者:钟微,Email:zhongwei@gwcmc.org