Ciliated hepatic foregut cysts in children

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Ciliated hepatic foregut cyst

Copyright C 2012 by The Korean Association for the Study of the Liver This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. Figure 1. Portal veno...

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Ciliated Hepatic Foregut Cyst with Obstructive Jaundice

Ciliated hepatic foregut cysts (CHFCs) are rare congenital cystic lesion that are most often solitary, unilocular, and located in the subcapsular region of the medial segment of the left hepatic lobe. The mucoid fluid contents affect imaging studies and often make definitive diagnosis difficult. CHFCs are usually asymptomatic and found incidentally. We report a 69-year-old female patient with a...

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The cancer-testis Sp17 and ASP are expressed in the ciliated hepatic foregut cysts

Although ciliated hepatic foregut cysts (CHFCs) are retained benign lesions, a case of squamous cell metaplasia and three cases of squamous cell carcinoma arising from CHFCs has been reported. The potential of malignant transformation make it necessary the identification of new biomarkers for more accurate management of CHFCs. Here we investigate the expression of Sperm protein 17 (Sp17) and AK...

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Foregut Duplication Cysts in Children

BACKGROUND AND OBJECTIVES Duplications of the alimentary tract are rare anomalies. We report our experience with foregut duplication cysts including their clinical presentation, diagnostic modalities, and surgical management. METHODS We report a 20-year retrospective review of all foregut duplication cysts managed at our institution. RESULTS Twelve patients with 13 foregut duplication cysts...

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Ciliated Hepatic Foregut Cyst: 103 Cases in the World Literature

Ciliated hepatic foregut cysts (CHFC) are rare, typically benign, lesions whose incidence has been increasing recently. Despite this increase in incidence, they remain rare and several key characteristics remain poorly understood, including the range of presentation and the risk of malignant conversion. To better understand CHFC, an extensive review of the international literature was performed...

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ژورنال

عنوان ژورنال: Pediatric Surgery International

سال: 2009

ISSN: 0179-0358,1437-9813

DOI: 10.1007/s00383-009-2468-x