Congenital Solitary Nonparasitic Cyst of the Liver in Infancy and Childhood

1995 ◽  
Vol 21 (4) ◽  
pp. 461-462 ◽  
Author(s):  
Nuran Pul ◽  
Mehmet Pul
1986 ◽  
Vol 5 (10) ◽  
pp. 585-587 ◽  
Author(s):  
P A Athey ◽  
J A Lauderman ◽  
D E King

2005 ◽  
Vol 40 (12) ◽  
pp. e27-e30 ◽  
Author(s):  
Yushi Otani ◽  
Hajime Takayasu ◽  
Yuki Ishimaru ◽  
Kaori Okamura ◽  
Junko Yamagishi ◽  
...  

2007 ◽  
Vol 23 (10) ◽  
pp. 1007-1009
Author(s):  
Takeshi Aoyagi ◽  
Fumiaki Sasaki ◽  
Tadao Okada ◽  
Toshiya Kamiyama ◽  
Tomoo Itoh ◽  
...  

1953 ◽  
Vol 137 (3) ◽  
pp. 410-415 ◽  
Author(s):  
LEON H. MANHEIMEB

2003 ◽  
Vol 6 (3) ◽  
pp. 265-269 ◽  
Author(s):  
Georgia M. Azar ◽  
N. Kutin ◽  
Ellen Kahn

We report a hepatic tumor in an adolescent that does not fit into any of the described categories of liver tumors. The patient presented with hepatomegaly, abdominal pain, and normal liver function test; the tumor was cystic in imaging studies. The resected specimen, result of a partial hepatectomy, measured 21 cm and was multicystic with solid areas. Microscopically, the cysts were lined by a mucous-producing or intestinal-type epithelium, associated with smooth muscle and small mucous-producing glands. The solid component contained fibrous and adipose tissue, smooth muscle and thick-walled vessels. Aneuploidy was demonstrated by flow cytometry. We interpreted the tumor as having features of a mesenchymal hamartoma and congenital solitary nonparasitic cyst. It is conceivable that the lesions originated with small peribiliary glands with dilatation and intestinal metaplasia.


1992 ◽  
Vol 22 (7) ◽  
pp. 543-544 ◽  
Author(s):  
S. P. Quillin ◽  
W. H. McAlister

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