Laparoscopic-Assisted Anorectal Pull-Through for Currarino Syndrome

被引:4
作者
Li, Qi [1 ]
Zhang, Zhen [1 ]
Jiang, Qian [2 ]
Yan, Yuchun [3 ]
Xiao, Ping [4 ]
Ma, Ya [5 ]
Li, Long [1 ]
机构
[1] Capital Inst Pediat, Dept Gen Surg, 2 Yabao Rd, Beijing 100020, Peoples R China
[2] Capital Inst Pediat, Dept Med Genet, Beijing, Peoples R China
[3] Capital Inst Pediat, Dept Radiol, Beijing, Peoples R China
[4] Capital Inst Pediat, Dept Pathol, Beijing, Peoples R China
[5] Capital Inst Pediat, Dept Ultrasound, Beijing, Peoples R China
来源
JOURNAL OF LAPAROENDOSCOPIC & ADVANCED SURGICAL TECHNIQUES | 2020年 / 30卷 / 07期
基金
中国国家自然科学基金;
关键词
laparoscopic-assisted anorectal pull-through; Currarino syndrome; SURGICAL-MANAGEMENT; ANORECTOPLASTY; TRIAD; MALFORMATIONS; CHILDREN; PHENOTYPE; SPECTRUM; HLXB9; GENE;
D O I
10.1089/lap.2019.0779
中图分类号
R61 [外科手术学];
学科分类号
摘要
Objective: Currarino syndrome (CS) is characterized by the triad of sacral anomalies, presacral tumor, and anorectal malformation (ARM). This study evaluates the feasibility and outcomes of laparoscopic-assisted anorectal pull-through (LAARP) for CS. Materials and Methods: Children admitted for primary or redo repair of CS through LAARP between 2016 and 2019 were reviewed. The indication of redo included constipation with megarectosigmoid, residual presacral mass, anastomosis leak, and secondary fistula. ARM was corrected by excision of rectal stenosis, fistula, and its associated megarectosigmoid. This was followed by a complete surgical resection of the presacral tumor, with subsequent pull-through and anocolic anastomosis. This was done with a combined laparoscopic and transanal approach. The detailed surgical techniques, early postoperative complications, and mid-term functional outcomes were summarized. Results: Fourteen patients underwent LAARP for primary (N = 4) and redo (N = 10) repair of CS. Four of them had colostomy previously. Mean age at operation was 20.7 +/- 13.9 months. Mean operative time was 120 +/- 25 minutes. Median hospital stay was 8 days (range 7-9 days) postoperatively. None of the patients developed early postoperative complications such as anastomotic leaks, presacral abscesses, recurrent fistulas, and residual mass. Bowel function was assessed 1 year after LAARP in 10 patients. Mean follow-up time was 15.9 months. The frequency of bowel movements was 3.3 +/- 1.5/day. Constipation occurred in 2 patients. Occasional soiling (<3 times/week) was reported in 4 patients and frequent soiling (>3 times/week) was in 1. Conclusion: LAARP for CS is safe and effective.
引用
收藏
页码:826 / 833
页数:8
相关论文
共 26 条
[1]   The Currarino triad: What pediatric surgeons need to know [J].
AbouZeid, Amr Abdelhamid ;
Mohammad, Shaimaa Abdelsattar ;
Abolfotoh, Mohammad ;
Radwan, Ahmed Bassiouny ;
Ismail, Mohamed Mohamed ElSayed ;
Hassan, Tarek Ahmed .
JOURNAL OF PEDIATRIC SURGERY, 2017, 52 (08) :1260-1268
[2]   Currarino triad associated with Hirschsprung's disease [J].
Baltogiannis, N ;
Mavridis, G ;
Soutis, M ;
Keramidas, D .
JOURNAL OF PEDIATRIC SURGERY, 2003, 38 (07) :1086-1089
[3]   Megarectosigmoid in children with anorectal malformations: Long term outcome after surgical or conservative treatment [J].
Borg, Helena ;
Bachelard, Marc ;
Sillen, Ulla .
JOURNAL OF PEDIATRIC SURGERY, 2014, 49 (04) :564-569
[4]   Megarectum after surgery for anorectal malformations [J].
Burjonrappa, Sathyaprasad ;
Youssef, Sami ;
Lapierre, Stephanie ;
Bensoussan, Arie ;
Bouchard, Sarah .
JOURNAL OF PEDIATRIC SURGERY, 2010, 45 (04) :762-768
[5]   Currarino syndrome: repair of the dysraphic anomalies and resection of the presacral mass in a combined neurosurgical and general surgical approach [J].
Cearns, Michael D. ;
Hettige, Samantha ;
De Coppi, Paolo ;
Thompson, Dominic N. P. .
JOURNAL OF NEUROSURGERY-PEDIATRICS, 2018, 22 (05) :584-590
[6]   Currarino syndrome: does the presence of a genetic anomaly correlate with a more severe phenotype? A multicentre study [J].
Costanzo, Sara ;
Spaccini, Luigina ;
Pio, Luca ;
Mattioli, Girolamo ;
Virgone, Calogero ;
Dall'Igna, Patrizia ;
Iacobelli, Barbara ;
Inserra, Alessandro ;
Brisighelli, Giulia ;
Fagnani, Anna Maria ;
Leva, Ernesto ;
Giannotti, Giulia ;
Cheli, Maurizio ;
Frumento, Paolo ;
Riccipetitoni, Giovanna .
JOURNAL OF PEDIATRIC SURGERY, 2017, 52 (10) :1591-1596
[7]   Spectrum of HLXB9 gene mutations in Currarino syndrome and genotype-phenotype correlation [J].
Cretolle, C. ;
Pelet, A. ;
Sanlaville, D. ;
Zerah, A. ;
Amiel, J. ;
Jaubert, E. ;
Revillon, Y. ;
Baala, L. ;
Munnich, A. ;
Nihou-Fekete, C. ;
Lyonnet, S. .
HUMAN MUTATION, 2008, 29 (07) :903-910
[8]   TRIAD OF ANORECTAL, SACRAL, AND PRESACRAL ANOMALIES [J].
CURRARINO, G ;
COLN, D ;
VOTTELER, T .
AMERICAN JOURNAL OF ROENTGENOLOGY, 1981, 137 (02) :395-398
[9]  
Dalmonte Giorgio, 2019, Acta Biomed, V90, P112, DOI 10.23750/abm.v90i1.7004
[10]   Congenital anomaly rectified at birth: one-stage single-incision laparoscopic-assisted anorectoplasty for newborns with anorectal malformations and recto-urethral fistula [J].
Diao, Mei ;
Li, Long ;
Ye, Mao ;
Guan, Kao-Ping ;
Wei, Yan-Dong ;
Cheng, Wei .
SURGICAL ENDOSCOPY AND OTHER INTERVENTIONAL TECHNIQUES, 2016, 30 (11) :5156-5164