Literature DB >> 15980636

Prenatal diagnosis of diastematomyelia in a 15-week-old fetus.

A A Biri1, A B Turp, M Kurdoğlu, O Himmetoğlu, N Tokgöz Ercan, S Balci.   

Abstract

OBJECTIVE: A case of prenatal diagnosis of diastematomyelia is presented.
METHODS: A case of fetal diastematomyelia, diagnosed by prenatal sonography, demonstrated the typical sonographic features of this condition. In this case it was detected at 15 weeks of gestation, and presented with a midline echogenic focus in the posterior region of the thoracolumbar spine.
RESULTS: The pregnancy was terminated by induction of labor. The fetus was female and there was a 1-cm long endurated hyperemic lesion at the back of the fetus. We confirmed the diagnosis of diastematomyelia after termination of pregnancy by plain chest and abdominal X-ray and also MRI scanning.
CONCLUSION: Isolated diastematomyelia is a rare form of spinal dysraphism characterized by a sagittal cleft in the spinal cord, conus medullaris and/or filum terminale with splaying of the posterior vertebral elements. Prenatal diagnosis of this anomaly is possible in the early mid-trimester by sonography, thus allowing for early surgical intervention and a favorable prognosis. (c) 2005 S. Karger AG, Basel

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Year:  2005        PMID: 15980636     DOI: 10.1159/000085081

Source DB:  PubMed          Journal:  Fetal Diagn Ther        ISSN: 1015-3837            Impact factor:   2.587


  2 in total

1.  Isolated Diastematomyelia - A Rare but Crucial Antenatal Diagnosis.

Authors: 
Journal:  Med J Armed Forces India       Date:  2011-07-21

2.  MRI diagnosis of diastematomyelia in a 78-year-old woman: Case report and literature review.

Authors:  Urszula Zaleska-Dorobisz; Joanna Bladowska; Anna Biel; Leszek W Pałka; Daniel Hołownia
Journal:  Pol J Radiol       Date:  2010-04
  2 in total

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