Spinal dysraphism as a new entity in VACTERL syndrome, resulting in a novel acronym VACTERLS

被引:9
作者
Amelot, Aymeric [1 ]
Cretolle, Celia [2 ,3 ]
de Saint Denis, Timothee [1 ]
Sarnacki, Sabine [2 ,3 ]
Catala, Martin [4 ,5 ,6 ]
Zerah, Michel [1 ,7 ,8 ]
机构
[1] Univ Paris 05, Necker EM Hosp, AP HP, Dept Pediat Neurosurg, Paris, France
[2] Univ Paris 05, Necker EM Hosp, AP HP, Dept Visceral Pediat Surg, Paris, France
[3] Univ Paris 05, Necker EM Hosp, AP HP, Reference Ctr AnoRectal & Rare Pelv Anomalies MAR, Paris, France
[4] UPMC, cUMR7622, Paris 05, France
[5] CNRS, Paris 05, France
[6] Grp Hosp Pitie Salpetriere, Federat Neurol, 47-83 Blvd Hop, Paris 13, France
[7] Univ Paris 05, Necker EM Hosp, AP HP, Reference Ctr Chiari & Malformat Spine & Spinal C, Paris, France
[8] Univ Paris 05, Necker EM Hosp, AP HP, Inst Genet Dis IMAGINE, Paris, France
关键词
VACTERL association; Anorectal malformation; Dysraphism; Spine; Lipoma; Urinary disorders; TETHERED CORD SYNDROME; IN-VITRO FERTILIZATION; ESOPHAGEAL ATRESIA; ANORECTAL-MALFORMATIONS; REPRODUCTIVE TECHNOLOGIES; VATER/VACTERL ASSOCIATION; VATER ASSOCIATION; FILUM TERMINALE; ANOMALIES; CHILDREN;
D O I
10.1007/s00431-020-03609-4
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Anorectal malformation (ARM) is the most common symptom in VACTERL syndrome (vertebral, anal, cardiac, tracheo-esophageal fistula, renal, and limb anomalies). The association of ARM and spinal dysraphisms (DYS) is well documented. We aim to better evaluate children with VACTERL association and ARM, considering the presence or not of DYS. Between 2000 and 2015, 279 children with VACTERL associations were identified in Necker Children's Hospital, Paris. We identified 61 VACTERL children (22%) with ARM. A total of 52 VACTERL children with ARM were included. DYS were identified in 36/52 of cases (69.2%). A total of 33 (63.5%) VACTERL children presented with sphincterial dysfunction. We constated that 28/33 (84.8%) of them had DYS + (p < 0.0001). More children in ARM (DYS +) subgroup are presenting with initial urinary sphincter dysfunction (58 vs 19%, p < 0.009) than ARM (DYS -). We identified 29 lipoma filum in our series, which were not statistically associated with urinary disorders (p = 0.143). Conclusion: We propose to refine the definition of VACTERL association, by adding S as Spinal defect to include it as an integral part of this syndrome, resulting in a novel acronym V.A.C.TE.R.L.S.What is Known:center dot The VACTERL association: congenital anomalies of the bony vertebral column (V), anorectal malformation (A), congenital cardiopathy (C), tracheo-esophageal defects (TE), renal and urinary tract anomalies (R), and limb malformations (L).center dot VACTERL children needs a complete appraisal, as early as possible, to adopt the most appropriate therapeutic management.What is New:center dot Include spine dysraphism (DYS) as a part of this syndrome, resulting in a novel acronym V.A.C.TE.R.L.S.center dot The significant correlation between VACTERL/DYS and urinary dysfunction requires to investigate the spine cord prenatally.
引用
收藏
页码:1121 / 1129
页数:9
相关论文
共 49 条
  • [1] Isolated lipoma of filum terminale in adults: MRI findings and clinical correlation
    Al-Omari, Ma'moon H.
    Eloqayli, Haytham M.
    Qudseih, Hana' M.
    Al-Shinag, Mohammad K.
    [J]. JOURNAL OF MEDICAL IMAGING AND RADIATION ONCOLOGY, 2011, 55 (03) : 286 - 290
  • [2] Quality of life for children with fecal incontinence after surgically corrected anorectal malformation
    Bai, YZ
    Yuan, ZW
    Wang, WL
    Zhao, YR
    Wang, HZ
    Wang, W
    [J]. JOURNAL OF PEDIATRIC SURGERY, 2000, 35 (03) : 462 - 464
  • [3] VATER/VACTERL association: identification of seven new twin pairs, a systematic review of the literature, and a classical twin analysis
    Bartels, Enrika
    Schulz, Anna C.
    Mora, Nicole W.
    Pineda-Alvarez, Daniel E.
    Wijers, Charlotte H. W.
    Marcelis, Carlo M.
    Stressig, Ruediger
    Ritgen, Jochen
    Schmiedeke, Eberhard
    Mattheisen, Manuel
    Draaken, Markus
    Hoffmann, Per
    Hilger, Alina C.
    Dworschak, Gabriel C.
    Baudisch, Friederike
    Ludwig, Michael
    Bagci, Soyhan
    Mueller, Andreas
    Gembruch, Ulrich
    Geipel, Annegret
    Berg, Christoph
    Bartmann, Peter
    Noethen, Markus M.
    van Rooij, Iris A. L. M.
    Solomon, Benjamin D.
    Reutter, Heiko M.
    [J]. CLINICAL DYSMORPHOLOGY, 2012, 21 (04) : 191 - 195
  • [4] VERTEBRAL ANOMALIES ASSOCIATED WITH ESOPHAGEAL ATRESIA AND TRACHEOESOPHAGEAL FISTULA WITH REFERENCE TO INITIAL OPERATIVE MORTALITY
    BONDTAYL.W
    STARER, F
    ATWELL, JD
    [J]. JOURNAL OF PEDIATRIC SURGERY, 1973, 8 (01) : 9 - 13
  • [5] A multi-centre cohort study of the physical health of 5-year-old children conceived after intracytoplasmic sperm injection, in vitro fertilization and natural conception
    Bonduelle, M
    Wennerholm, UB
    Loft, A
    Tarlatzis, BC
    Peters, C
    Henriet, S
    Mau, C
    Victorin-Cederquist, A
    Van Steirteghem, A
    Balaska, A
    Emberson, JR
    Sutcliffe, AG
    [J]. HUMAN REPRODUCTION, 2005, 20 (02) : 413 - 419
  • [6] Clinical and etiological heterogeneity in patients with tracheo-esophageal malformations and associated anomalies
    Brosens, Erwin
    Ploeg, Mirjam
    van Bever, Yolande
    Koopmans, Anna E.
    IJsselstijn, Hanneke
    Rottier, Robbert J.
    Wijnen, Rene
    Tibboel, Dick
    de Klein, Annelies
    [J]. EUROPEAN JOURNAL OF MEDICAL GENETICS, 2014, 57 (08) : 440 - 452
  • [7] IMPERFORATE ANUS - THE NEUROLOGIC IMPLICATION OF SACRAL ABNORMALITIES
    CARSON, JA
    BARNES, PD
    TUNELL, WP
    SMITH, EI
    JOLLEY, SG
    [J]. JOURNAL OF PEDIATRIC SURGERY, 1984, 19 (06) : 838 - 842
  • [8] Genetic control of caudal development
    Catala, M
    [J]. CLINICAL GENETICS, 2002, 61 (02) : 89 - 96
  • [9] The genetic landscape and clinical implications of vertebral anomalies in VACTERL association
    Chen, Yixin
    Liu, Zhenlei
    Chen, Jia
    Zuo, Yuzhi
    Liu, Sen
    Chen, Weisheng
    Liu, Gang
    Qiu, Guixing
    Giampietro, Philip F.
    Wu, Nan
    Wu, Zhihong
    [J]. JOURNAL OF MEDICAL GENETICS, 2016, 53 (07) : 431 - 437
  • [10] One hundred three consecutive patients with anorectal malformations and their associated anomalies
    Cho, S
    Moore, SP
    Fangman, T
    [J]. ARCHIVES OF PEDIATRICS & ADOLESCENT MEDICINE, 2001, 155 (05): : 587 - 591