AJP Rep 2014; 04(02): e89-e92
DOI: 10.1055/s-0034-1394151
Case Report
Thieme Medical Publishers 333 Seventh Avenue, New York, NY 10001, USA.

Counseling a Patient with the Antenatal Diagnosis of a Cerebellar Abnormality and a Pharyngeal Cyst

Lissa Francois
1   Department of Obstetrics, Gynecology and Reproductive Sciences, Rutgers-Robert Wood Johnson Medical School, New Brunswick, New Jersey
,
Rachanna Tyagi
2   Department of Pediatric Neurosurgery, Rutgers-Robert Wood Johnson Medical School, New Brunswick, New Jersey
,
Thomas Hegyi
3   Division of Neonatology, Department of Pediatrics, SIDS Center of New Jersey, Rutgers-Robert Wood Johnson Medical School, New Brunswick, New Jersey
,
Joaquin Santolaya-Forgas
1   Department of Obstetrics, Gynecology and Reproductive Sciences, Rutgers-Robert Wood Johnson Medical School, New Brunswick, New Jersey
› Author Affiliations
Further Information

Publication History

19 May 2014

18 August 2014

Publication Date:
18 November 2014 (online)

Abstract

Introduction Prenatal counseling with regards to the prognosis of a cerebellar abnormality is hindered not only by the diverse clinical presentations but also by the presence of subtle findings. We present a case of a distinct combination of asymmetric cerebellar hypoplasia secondary to an anterior meningoencephalocele through a clival defect that caused a severe airway obstruction in the newborn.

Case Description A 21-year-old gravida 4 para 0 mother with a dichorionic–diamniotic twin pregnancy was referred for a second trimester sonographic survey. An asymmetric cerebellar hypoplasia, mega cisterna magna, and a pharyngeal cystic mass were noted on twin A. Magnetic resonance imaging report confirmed posterior fossa abnormalities and shed no light on the differential diagnosis of the cystic mass. The pregnancy ended by Cesarean delivery at 32 weeksʼ gestation after a preterm premature rupture of the membranes. Twin A had a severe airway obstruction. Postnatal evaluation confirmed a midline anterior meningoencephalocele through a defect in the clivus. The microarray chromosomal analysis demonstrated a 5q15 variant with uncertain clinical significance.

Conclusion Antenatal recognition of the unique combination of a cerebellar hypoplasia with a pharyngeal cyst can impact the prenatal counseling as well as neonatal management.

 
  • References

  • 1 Long A, Moran P, Robson S. Outcome of fetal cerebral posterior fossa anomalies. Prenat Diagn 2006; 26 (8) 707-710
  • 2 Copp AJ. Neurulation in the cranial region—normal and abnormal. J Anat 2005; 207 (5) 623-635
  • 3 Greene ND, Copp AJ. Development of the vertebrate central nervous system: formation of the neural tube. Prenat Diagn 2009; 29 (4) 303-311
  • 4 Baisakhiya N, Deshmukh P, Pawar V. Tornwaldt cyst: a cause of neck pain and stiffness. Indian J Otolaryngol Head Neck Surg 2011; 63 (Suppl. 01) 147-148
  • 5 Rustamzadeh E, Graupman PC, Lam CH. Basicranial diplomyelia: an extension of the split cord malformation theory. Case report. J Neurosurg 2006; 104 (5, Suppl): 362-365
  • 6 Carroll EA, Gerrelli D, Gasca S , et al. Cordon-bleu is a conserved gene involved in neural tube formation. Dev Biol 2003; 262 (1) 16-31
  • 7 Fleming A, Copp AJ. A genetic risk factor for mouse neural tube defects: defining the embryonic basis. Hum Mol Genet 2000; 9 (4) 575-581
  • 8 Massa V, Savery D, Ybot-Gonzalez P , et al. Apoptosis is not required for mammalian neural tube closure. Proc Natl Acad Sci U S A 2009; 106 (20) 8233-8238
  • 9 Dunlevy LP, Burren KA, Mills K, Chitty LS, Copp AJ, Greene ND. Integrity of the methylation cycle is essential for mammalian neural tube closure. Birth Defects Res A Clin Mol Teratol 2006; 76 (7) 544-552