Published online Jul 16, 2013. doi: 10.12998/wjcc.v1.i4.152
Revised: June 4, 2013
Accepted: June 8, 2013
Published online: July 16, 2013
A hepatic lymphangioma is a rare benign neoplasm and is usually associated with lymphangiomas of other viscera. A hepatic lymphangioma can be solitary, cystic or associated with multiple liver lesions and is characterized by cystic dilatation of lymphatic vessels in the hepatic parenchyma. A solitary lymphangioma is unusual. Here we report a rare case of a solitary huge primary hepatic cystic lymphangioma in a 42-year-old woman. It was discovered on routine physical examination and the patient had no obvious symptoms. Ultrasonography and computed tomography (CT) showed a giant “hepatic neoplasm” that occupied the right liver lobe. The lesion was approximately 20.0 cm × 15.0 cm × 10.0 cm in size and contained cystic and solid components. There were multiple septa inside the tumor, with some calcifications in the septa. Surgical resection was performed. Histological examination revealed multiple cystic structures lined with epithelial cells on the inner walls, accompanied by interstitial swelling and necrosis. The patient has now been followed up for nearly two years after surgery, with no recurrence to date.
Core tip: Lymphangiomas are congenital malformations of the lymphatic system. A hepatic lymphangioma is a rare benign neoplasm that is usually associated with lymphangiomas of other viscera. A solitary lymphangioma is unusual. Here, we report a rare case of a solitary huge primary hepatic cystic lymphangioma. It was discovered on routine physical examination and the patient had no obvious symptoms. The diagnosis was confirmed by histological examination. The patient has now been followed up for nearly two years after surgery and has had no recurrence.