Eur J Pediatr Surg 2010; 20(3): 196-198
DOI: 10.1055/s-0029-1237733
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© Georg Thieme Verlag KG Stuttgart · New York

Congenital Intercostal Liver Herniation: Report on two Neonates

G. Ertan1 , M. Sinzig2 , A. Tekes1 , T. A. G. M. Huisman1
  • 1Johns Hopkins Medical Institutions, Pediatric Radiology, Baltimore, United States
  • 2Klagenfurt Hospital, Division of Pediatric Radiology, Klagenfurt, Austria
Further Information

Publication History

Publication Date:
30 October 2009 (online)

Introduction

Congenital herniation of the liver or parts of the liver through the chest wall is an extremely rare entity. The exact etiology of congenital intercostal liver herniation (CILH) is unknown [1] [2]. Herniation of the liver or parts of the liver into the chest cavity is well known as a complication of congenital or post traumatic diaphragmatic hernia (CDH) [3] [4] [5]. We report on two unusual cases of right-sided CILH with an intact diaphragm. In both neonates the ipsilateral diaphragm was eventrated. Congenital diaphragmatic eventration (CDE) is defined as an abnormal elevation of an intact hemidiaphram [6]. Preoperative computer tomography (CT) allows correct identification of CILH with CDE.

References

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Correspondence

Prof. Dr. Thierry AGM Huisman

Medical Director

Divison of Pediatric Radiology

Johns Hopkins Hospital

600 North Wolfe Street

Nelson B-173

Baltimore, md 21287 – 0842

Phone: +001-410-9556140

Fax: +001-410-502-3633

Email: thuisma1@jhmi.edu

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