Neurenteric cyst - a case report of this rare disorder

M. Schurink, M. Y. A. van Herwaarden-Lindeboom, M. H. Coppes, A. G. Veldhuizen, H. A. Koetse, Z. J. de Langen*

*Corresponding author for this work

    Research output: Contribution to journalArticleAcademicpeer-review

    8 Citations (Scopus)

    Abstract

    Neurenteric cysts are rare congenital lesions that are believed to be the result of the split notochord syndrome. We report the clinical case of a 5-year-old boy presenting with vague gastrointestinal symptoms and fatigue, who had undergone resection of a small intestine duplication cyst as a newborn. Computed tomography revealed a mediastinal neurenteric cyst with partial destruction of several thoracic vertebrae. Resection of the tumor proved effective. Recognition of this disorder is important because of its benign nature, the prognosis after surgical resection can be good. If the diagnosis is made in an early stage, unnecessary progressive destruction of surrounding structures may be prevented. (C) 2007 Elsevier Inc. All rights reserved.

    Original languageEnglish
    Number of pages5
    JournalJournal of Pediatric Surgery
    Volume42
    Issue number5
    DOIs
    Publication statusPublished - May-2007

    Keywords

    • neurenteric cyst
    • intestinal duplication
    • notochord syndrome

    Cite this