A case of prenatally diagnosed limited dorsal myeloschisis with good prognosis

J Clin Ultrasound. 2018 May;46(4):282-285. doi: 10.1002/jcu.22527. Epub 2017 Oct 5.

Abstract

Diagnosis of fetal spinal dysraphism is a challenge. It is difficult to distinguish between a meningocele, myelomeningocele, and a recently described entity called limited dorsal myeloschisis (LDM). Although myelomeningocele is associated with a poor prognosis, LDM can have a good outcome. We present a case of prenatally diagnosed LDM. Because sonographic examination revealed a round, cystic, septated cervical mass without associated cerebral anomalies, the lesion was initially considered an isolated meningocele. Fetal MRI contributed to correct the diagnosis. A diagnostic error can lead to the wrong surgical support or even the termination of pregnancy. Therefore, we highlight the importance of fetal MRI in such cases, particularly when no cerebral abnormalities are observed on sonographic examination.

Keywords: limited dorsal myeloschisis; obstetrics; sonography; spinal dysraphism.

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Diagnosis, Differential
  • Female
  • Humans
  • Magnetic Resonance Imaging*
  • Pregnancy
  • Prognosis
  • Spinal Dysraphism / diagnostic imaging*
  • Ultrasonography, Prenatal*