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Erschienen in: European Journal of Pediatrics 7/2020

13.02.2020 | Original Article

Spinal dysraphism as a new entity in V.A.C.TE.R.L syndrome, resulting in a novel acronym V.A.C.TE.R.L.S

verfasst von: Aymeric Amelot, Célia Cretolle, Timothée de Saint Denis, Sabine Sarnacki, Martin Catala, Michel Zerah

Erschienen in: European Journal of Pediatrics | Ausgabe 7/2020

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Abstract

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:
• 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).
• VACTERL children needs a complete appraisal, as early as possible, to adopt the most appropriate therapeutic management.
What is New:
• Include spine dysraphism (DYS) as a part of this syndrome, resulting in a novel acronym V.A.C.TE.R.L.S.
• The significant correlation between VACTERL/DYS and urinary dysfunction requires to investigate the spine cord prenatally.
Literatur
1.
Zurück zum Zitat Quan L, Smith DW (1973) The VATER association. Vertebral defects, anal atresia, T-E fistula with esophageal atresia, radial and renal dysplasia: a spectrum of associated defects. J Pediatr 82:104–107CrossRef Quan L, Smith DW (1973) The VATER association. Vertebral defects, anal atresia, T-E fistula with esophageal atresia, radial and renal dysplasia: a spectrum of associated defects. J Pediatr 82:104–107CrossRef
2.
Zurück zum Zitat Temtamy SA, Miller JD (1974) Extending the scope of the VATER association: definition of the VATER syndrome. J Pediatr 85:345–349CrossRef Temtamy SA, Miller JD (1974) Extending the scope of the VATER association: definition of the VATER syndrome. J Pediatr 85:345–349CrossRef
8.
Zurück zum Zitat Levitt MA, Patel M, Rodriguez G, Gaylin DS, Pena A (1997) The tethered spinal cord in patients with anorectal malformations. J Pediatr Surg 32:462–468CrossRef Levitt MA, Patel M, Rodriguez G, Gaylin DS, Pena A (1997) The tethered spinal cord in patients with anorectal malformations. J Pediatr Surg 32:462–468CrossRef
9.
Zurück zum Zitat Rivosecchi M, Lucchetti MC, Zaccara A, de Gennaro M, Fariello G (1995) Spinal dysraphism detected by magnetic resonance imaging in patients with anorectal anomalies: incidence and clinical significance. J Pediatr Surg 30:488–490CrossRef Rivosecchi M, Lucchetti MC, Zaccara A, de Gennaro M, Fariello G (1995) Spinal dysraphism detected by magnetic resonance imaging in patients with anorectal anomalies: incidence and clinical significance. J Pediatr Surg 30:488–490CrossRef
10.
Zurück zum Zitat Valentini LG, Selvaggio G, Erbetta A et al (2013) Occult spinal dysraphism: lessons learned by retrospective analysis of 149 surgical cases about natural history, surgical indications, urodynamic testing, and intraoperative neurophysiological monitoring. Childs Nerv Syst ChNS Off J Int Soc Pediatr Neurosurg 29:1657–1669. https://doi.org/10.1007/s00381-013-2186-5 CrossRef Valentini LG, Selvaggio G, Erbetta A et al (2013) Occult spinal dysraphism: lessons learned by retrospective analysis of 149 surgical cases about natural history, surgical indications, urodynamic testing, and intraoperative neurophysiological monitoring. Childs Nerv Syst ChNS Off J Int Soc Pediatr Neurosurg 29:1657–1669. https://​doi.​org/​10.​1007/​s00381-013-2186-5 CrossRef
12.
17.
Zurück zum Zitat Bond-Taylor W, Starer F, Atwell JD (1973) Vertebral anomalies associated with esophageal atresia and tracheoesophageal fistula with reference to the initial operative mortality. J Pediatr Surg 8:9–13CrossRef Bond-Taylor W, Starer F, Atwell JD (1973) Vertebral anomalies associated with esophageal atresia and tracheoesophageal fistula with reference to the initial operative mortality. J Pediatr Surg 8:9–13CrossRef
18.
Zurück zum Zitat Stevenson RE (1974) The association of extra vertebras and tracheoesophageal anomalies. Birth Defects Orig Artic Ser 10:147–148PubMed Stevenson RE (1974) The association of extra vertebras and tracheoesophageal anomalies. Birth Defects Orig Artic Ser 10:147–148PubMed
19.
Zurück zum Zitat Louhimo I, Lindahl H (1983) Esophageal atresia: primary results of 500 consecutively treated patients. J Pediatr Surg 18:217–229CrossRef Louhimo I, Lindahl H (1983) Esophageal atresia: primary results of 500 consecutively treated patients. J Pediatr Surg 18:217–229CrossRef
20.
Zurück zum Zitat German JC, Mahour GH, Woolley MM (1976) Esophageal atresia and associated anomalies. J Pediatr Surg 11:299–306CrossRef German JC, Mahour GH, Woolley MM (1976) Esophageal atresia and associated anomalies. J Pediatr Surg 11:299–306CrossRef
24.
Zurück zum Zitat Uehling DT, Gilbert E, Chesney R (1983) Urologic implications of the VATER association. J Urol 129:352–354CrossRef Uehling DT, Gilbert E, Chesney R (1983) Urologic implications of the VATER association. J Urol 129:352–354CrossRef
25.
Zurück zum Zitat Davidoff AM, Thompson CV, Grimm JM, Shorter NA, Filston HC, Oakes WJ (1991) Occult spinal dysraphism in patients with anal agenesis. J Pediatr Surg 26:1001–1005CrossRef Davidoff AM, Thompson CV, Grimm JM, Shorter NA, Filston HC, Oakes WJ (1991) Occult spinal dysraphism in patients with anal agenesis. J Pediatr Surg 26:1001–1005CrossRef
27.
Zurück zum Zitat Cho S, Moore SP, Fangman T (2001) One hundred three consecutive patients with anorectal malformations and their associated anomalies. Arch Pediatr Adolesc Med 155:587–591CrossRef Cho S, Moore SP, Fangman T (2001) One hundred three consecutive patients with anorectal malformations and their associated anomalies. Arch Pediatr Adolesc Med 155:587–591CrossRef
28.
Zurück zum Zitat Tortori-Donati P, Rossi A, Cama A (2000) Spinal dysraphism: a review of neuroradiological features with embryological correlations and proposal for a new classification. Neuroradiology 42:471–491CrossRef Tortori-Donati P, Rossi A, Cama A (2000) Spinal dysraphism: a review of neuroradiological features with embryological correlations and proposal for a new classification. Neuroradiology 42:471–491CrossRef
29.
Zurück zum Zitat Carson JA, Barnes PD, Tunell WP, Smith EI, Jolley SG (1984) Imperforate anus: the neurologic implication of sacral abnormalities. J Pediatr Surg 19:838–842CrossRef Carson JA, Barnes PD, Tunell WP, Smith EI, Jolley SG (1984) Imperforate anus: the neurologic implication of sacral abnormalities. J Pediatr Surg 19:838–842CrossRef
40.
Zurück zum Zitat Bartels E, Schulz AC, Mora NW, Pineda-Alvarez DE, Wijers CH, Marcelis CM, Stressig R, Ritgen J, Schmiedeke E, Mattheisen M, Draaken M, Hoffmann P, Hilger AC, Dworschak GC, Baudisch F, Ludwig M, Bagci S, Müller A, Gembruch U, Geipel A, Berg C, Bartmann P, Nöthen MM, van Rooij I, Solomon BD, Reutter HM (2012) VATER/VACTERL association: identification of seven new twin pairs, a systematic review of the literature, and a classical twin analysis. Clin Dysmorphol 21:191–195. https://doi.org/10.1097/MCD.0b013e328358243c CrossRefPubMedPubMedCentral Bartels E, Schulz AC, Mora NW, Pineda-Alvarez DE, Wijers CH, Marcelis CM, Stressig R, Ritgen J, Schmiedeke E, Mattheisen M, Draaken M, Hoffmann P, Hilger AC, Dworschak GC, Baudisch F, Ludwig M, Bagci S, Müller A, Gembruch U, Geipel A, Berg C, Bartmann P, Nöthen MM, van Rooij I, Solomon BD, Reutter HM (2012) VATER/VACTERL association: identification of seven new twin pairs, a systematic review of the literature, and a classical twin analysis. Clin Dysmorphol 21:191–195. https://​doi.​org/​10.​1097/​MCD.​0b013e328358243c​ CrossRefPubMedPubMedCentral
44.
Zurück zum Zitat Catala M (2002) Genetic control of caudal development. Clin Genet 61:89–96CrossRef Catala M (2002) Genetic control of caudal development. Clin Genet 61:89–96CrossRef
45.
Zurück zum Zitat Kim PC, Mo R, Hui Cc C (2001) Murine models of VACTERL syndrome: role of sonic hedgehog signaling pathway. J Pediatr Surg 36:381–384CrossRef Kim PC, Mo R, Hui Cc C (2001) Murine models of VACTERL syndrome: role of sonic hedgehog signaling pathway. J Pediatr Surg 36:381–384CrossRef
49.
Zurück zum Zitat Bonduelle M, Wennerholm U-B, Loft A et al (2005) 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. Hum Reprod Oxf Engl 20:413–419. https://doi.org/10.1093/humrep/deh592 CrossRef Bonduelle M, Wennerholm U-B, Loft A et al (2005) 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. Hum Reprod Oxf Engl 20:413–419. https://​doi.​org/​10.​1093/​humrep/​deh592 CrossRef
Metadaten
Titel
Spinal dysraphism as a new entity in V.A.C.TE.R.L syndrome, resulting in a novel acronym V.A.C.TE.R.L.S
verfasst von
Aymeric Amelot
Célia Cretolle
Timothée de Saint Denis
Sabine Sarnacki
Martin Catala
Michel Zerah
Publikationsdatum
13.02.2020
Verlag
Springer Berlin Heidelberg
Erschienen in
European Journal of Pediatrics / Ausgabe 7/2020
Print ISSN: 0340-6199
Elektronische ISSN: 1432-1076
DOI
https://doi.org/10.1007/s00431-020-03609-4

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