A Case Report of a Ciliated Hepatic Foregut Cyst in the Liver

2008 ◽  
Vol 58 (1) ◽  
pp. 87 ◽  
Author(s):  
Kyu Chan Oh ◽  
Won Kyu Park ◽  
Jay Chun Jang ◽  
Joon Hyuk Choi ◽  
Dong Shik Lee ◽  
...  
HPB ◽  
2021 ◽  
Vol 23 ◽  
pp. S996
Author(s):  
C. Silva ◽  
J. Silva ◽  
C. Robalo ◽  
J. Oliveira ◽  
C. Branco ◽  
...  

2001 ◽  
Vol 26 (6) ◽  
pp. 594-596 ◽  
Author(s):  
M. Hirata ◽  
H. Ishida ◽  
K. Konno ◽  
S. Nishiura

2000 ◽  
Vol 43 (1) ◽  
pp. 77 ◽  
Author(s):  
Hyo Sung Kwak ◽  
Jeong Min Lee ◽  
In Hwan Kim ◽  
Woo Sung Moon

2015 ◽  
Vol 4 (4) ◽  
pp. 467-469 ◽  
Author(s):  
Nicholas E. Bruns ◽  
Sofya H. Asfaw ◽  
Kathryn A. Stackhouse ◽  
Gavin A. Falk ◽  
David K. Magnuson ◽  
...  

1999 ◽  
Vol 123 (11) ◽  
pp. 1115-1117 ◽  
Author(s):  
Dan J. Vick ◽  
Zachary D. Goodman ◽  
Kamal G. Ishak

Abstract Ciliated hepatic foregut cysts are rare congenital lesions derived from the embryologic foregut. They are considered benign, and a review of 64 published cases revealed no instances of malignant transformation. We report a case of squamous cell carcinoma arising in a ciliated hepatic foregut cyst in a 51-year-old man. The tumor was found during a routine cholecystectomy and involved the adjacent mesentery and duodenal wall. There was histologic evidence of perineural and perivascular involvement. Despite an en bloc resection of the tumor and contiguous areas of gross involvement, the patient died 2 months later. Although aspiration of cyst contents is an accepted treatment for asymptomatic lesions, this case suggests that most ciliated hepatic foregut cysts should be excised, especially when radiologic studies yield equivocal results.


2019 ◽  
Vol 2019 ◽  
pp. 1-4
Author(s):  
Thomas Enke ◽  
Wuttiporn Manatsathit ◽  
Shaheed Merani ◽  
Kurt Fisher

Ciliated hepatic foregut cyst (CHFC) is a rare benign cyst of the liver derived from an embryonic remnant of foregut epithelium. CHFC is typically asymptomatic and is found incidentally. Recent reports of malignant transformation may warrant surgical removal of CHFC. We present the case of a 54-year-old male who was discovered to have a CHFC while undergoing kidney transplant evaluation.


2006 ◽  
Vol 41 (6) ◽  
pp. 1180-1183 ◽  
Author(s):  
Mark D. Stringer ◽  
Matthew O. Jones ◽  
Helen Woodley ◽  
Judy Wyatt

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