Nasal encephalocele in a child with Beckwith–Wiedemann syndrome

Author:

Broekman Marike L. D.12,Hoving Eelco W.3,Kho Kuan H.12,Speleman Lucienne4,Han K. Sen12,Hanlo Patrick W.12

Affiliation:

1. Rudolf Magnus Institute of Neuroscience and

2. Departments of Neurosurgery,

3. Department of Neurosurgery, University Medical Center Groningen, The Netherlands

4. Head and Neck Surgery, University Medical Center Utrecht; and

Abstract

✓ Beckwith–Wiedemann syndrome (BWS) is a rare congenital syndrome characterized by gigantism, macroglossia, exophthalmos, postpartum hypoglycemia, and multiple midline defects such as omphalocele. The authors describe, to the best of their knowledge, the first case of a child in whom BWS was diagnosed and who was subsequently treated for a nasal encephalocele. Because the authors believe that this feature might not be an incidental finding in patients with BWS, intranasal masses in these patients should be carefully differentiated, as complications might be severe.

Publisher

Journal of Neurosurgery Publishing Group (JNSPG)

Subject

General Medicine

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