Ciliated Hepatic Foregut Cyst: 103 Cases in the World Literature

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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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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: a report of 6 cases and a review of the English literature

BACKGROUND Ciliated hepatic foregut cyst (CHFC) is a rare cystic lesion most commonly identified in segment 4 of the liver that arises from the embryonic foregut. The classic histologic pattern is comprised of 4 distinct layers (inner ciliated epithelial lining, smooth muscle, loose connective tissue, fibrous capsule). Although rare, cases of metaplastic and malignant epithelial lining have bee...

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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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Ciliated Hepatic Foregut Cyst: Two Case Reports in Children and Review of the Literature

Ciliated hepatic foregut cyst (CHFC) is a rare lesion which originates from detached hepatic diverticulum or from detachment and migration of buds from the esophageal and bronchial regions of the foregut which subsequently get entrapped by the liver during the early embryonic development of the foregut. CHFCs are mostly seen in adults and are rarely reported in children, with only about 10 case...

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ژورنال

عنوان ژورنال: Open Journal of Pathology

سال: 2012

ISSN: 2164-6775,2164-6783

DOI: 10.4236/ojpathology.2012.23010