
Split notochord syndrome associated with dorsal neuroenteric fistula: A rare entity
Author(s) -
P. K. Srivastava,
A. N. Gangopadhyay,
Dheeraj Gupta,
Seema Sharma
Publication year - 2010
Publication title -
journal of pediatric neurosciences
Language(s) - English
Resource type - Journals
eISSN - 1998-3948
pISSN - 1817-1745
DOI - 10.4103/1817-1745.76112
Subject(s) - medicine , notochord , fistula , lumbosacral joint , dorsum , anatomy , surgery , biology , embryo , embryogenesis , microbiology and biotechnology
Split notochord syndrome (SNS) is an extremely rare congenital malformation associated with anomalies of the vertebral column, gastrointestinal tract and central nervous system. Twenty cases of SNS associated with dorsal enteric fistula have been reported in literature till date. The present report describes a unique case of SNS associated with lumbosacral meningomyelocele, dorsal neuroenteric fistula and dorsal herniation of right kidney along with vessels. The neonate was well managed by excision of enteric fistula, closure of duramater of meningomyelocele and repair of posterior wall hernia after placement of kidney in renal fossa. This kind of entity is uncommon and not been reported earlier.