BACKGROUND: The aim of the study was to review the degree to which the long-term outcome and ongoing morbidity in Currarino syndrome (CS) has been established. METHODS: Analysis of previously published reports that have included long-term outcome data in CS and review of five additional patients with CS. RESULTS: Overall, long-term outcomes of children born with CS are not well described. Malignancy has been reported in six children of approximately 300 CS patients: four children with malignancy had a recurrence after primary excision. Malignancy has also occurred in four adults. Ongoing morbidity related to constipation, faecal incontinence, neurogenic bladder, urinary incontinence and presacral abscess, and more rarely meningitis, brain metastases, developmental delay and unusual gait. Almost certainly, previous reports have under-estimated the true incidence of these problems, given the methodology and focus of these series. CONCLUSIONS: There is paucity of information on the long-term outcomes in CS. Few authors have focused on ongoing symptoms, such that we speculate the true incidence of long-term urinary and bowel dysfunction may have been under-estimated in CS. Greater emphasis on the functional assessment of these systems during childhood may help predict the long-term outcome in CS. The most severe cases are diagnosed during infancy and childhood, and these are also the ones who are more likely to have ongoing long-term morbidity.
BACKGROUND: The aim of the study was to review the degree to which the long-term outcome and ongoing morbidity in Currarino syndrome (CS) has been established. METHODS: Analysis of previously published reports that have included long-term outcome data in CS and review of five additional patients with CS. RESULTS: Overall, long-term outcomes of children born with CS are not well described. Malignancy has been reported in six children of approximately 300 CS patients: four children with malignancy had a recurrence after primary excision. Malignancy has also occurred in four adults. Ongoing morbidity related to constipation, faecal incontinence, neurogenic bladder, urinary incontinence and presacral abscess, and more rarely meningitis, brain metastases, developmental delay and unusual gait. Almost certainly, previous reports have under-estimated the true incidence of these problems, given the methodology and focus of these series. CONCLUSIONS: There is paucity of information on the long-term outcomes in CS. Few authors have focused on ongoing symptoms, such that we speculate the true incidence of long-term urinary and bowel dysfunction may have been under-estimated in CS. Greater emphasis on the functional assessment of these systems during childhood may help predict the long-term outcome in CS. The most severe cases are diagnosed during infancy and childhood, and these are also the ones who are more likely to have ongoing long-term morbidity.
Authors: Alexander Volk; Mohsen Karbasiyan; Alexander Semmler; Unda Todt; Horst Urbach; Thomas Klockgether; Michael Linnebank Journal: Birth Defects Res A Clin Mol Teratol Date: 2007-03
Authors: Pieter J Emans; Gauke Kootstra; Carlo L M Marcelis; Emile A M Beuls; L W Ernest van Heurn Journal: J Pediatr Surg Date: 2005-08 Impact factor: 2.545
Authors: C Crétolle; A Pelet; D Sanlaville; M Zérah; J Amiel; F Jaubert; Y Révillon; L Baala; A Munnich; C Nihoul-Fékété; S Lyonnet Journal: Hum Mutat Date: 2008-07 Impact factor: 4.878
Authors: Miguel Urioste; M del Carmen Garcia-Andrade; Laura Valle; Mercedes Robledo; Fernando González-Palacios; Ramiro Méndez; Joaquin Ferreirós; Javier Nuño; Javier Benítez Journal: Am J Med Genet A Date: 2004-07-30 Impact factor: 2.802