منابع مشابه
A Rare Case of Split Notochord Syndrome
We treated a one day old baby presenting with an extensive lumbosacral deformity, hydrocephalus and apparent enteric segments in the dorsal midline with abnormal genitalia, accompanied by an enteric fistula and imperforated anus. The malformation fits into split notochord syndrome. The baby died as a result of sepsis before surgical treatment could be attempted. Patient was full term caesarian ...
متن کاملSplit notochord syndrome: a case in point
A 36-year-old female presented with low back pain and was admitted. During the anamnesis, she reported having undergone surgery, in the first days of life, for the repair of lumbosacral myelomeningocele and imperforate anus. She had been a full-term infant, born to an adolescent mother who had received no prenatal care. There were no reports of infection, drug use, or exposure to teratogenic ag...
متن کامل[A rare variant of neuroenteric cyst: split notochord syndrome].
OBJECTIVE We present a case of split notochord syndrome, an extremely rare form of spinal dysraphism. DESCRIPTION We treated a 2 month-old boy presenting with an extensive lumbosacral deformity, hydrocephalus and apparent enteric segments in the dorsal midline, accompanied by an enteric fistula and imperforated anus. The malformation was diagnosed as split notochord syndrome. The baby died as...
متن کاملA case of split notochord syndrome: a child with a neuroenteric fistula presenting with meningitis.
The authors describe a case of split notochord syndrome with a neuroenteric fistula in a newborn presenting with meningitis. Associated anomalies included agenesis of the corpus callosum, short colon, malrotation, epispadias, and an abnormally high bifurcation of the abdominal aorta and inferior vena cava. The embryological mechanisms and etiologic theories are discussed in short.
متن کاملA case of split notochord syndrome: Presenting with respiratory failure in the neonatal period.
Split notochord syndrome (SNS) is a very rare congenital anomaly. This report describes a male newborn with a neuroenteric cyst in the posterior mediastinum and multiple vertebrae anomalies presenting with respiratory failure and pulmonary hypertension. This report also discusses the embryological development and the etiologic theories of SNS.
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ژورنال
عنوان ژورنال: Journal of Neonatal Surgery
سال: 2016
ISSN: 2226-0439
DOI: 10.21699/jns.v6i1.487