Case report of solitary giant hepatic lymphangioma.
10.14701/kjhbps.2016.20.2.71
- Author:
Hwan Hyo LEE
1
;
Seon Youl LEE
Author Information
1. Department of Surgery, Gimpo Woori Hospital, Gimpo, Korea.
- Publication Type:Case Report
- Keywords:
Lymphangioma;
Liver
- MeSH:
Abdominal Pain;
Adult;
Cystadenocarcinoma;
Cystadenoma;
Diagnosis;
Emergency Service, Hospital;
Female;
Hepatectomy;
Humans;
Liver;
Lymphangioma*;
Lymphangioma, Cystic;
Prognosis;
Recurrence
- From:Korean Journal of Hepato-Biliary-Pancreatic Surgery
2016;20(2):71-74
- CountryRepublic of Korea
- Language:English
-
Abstract:
A hepatic lymphangioma is a rare benign neoplasm that is usually associated with systemic lymphangiomatosis. A solitary hepatic lymphangioma is extremely rare. Therefore, we present a rare case of a female patient who underwent right hepatectomy for solitary giant hepatic lymphangioma. A 42-year-old female presented to the emergency department with complaint of severe abdominal pain of the right upper quadrant. Abdominal computed tomography showed an approximately 23×30-cm sized, giant, relatively well-defined, homogenous cystic mass with few septa in the right liver (segments VII and VIII). The preoperative diagnosis was a giant hepatic cystadenoma or cystadenocarcinoma. We performed right hepatectomy. The permanent histopathological report revealed cystic lymphangioma of the liver. Although the prognosis of solitary hepatic lymphangioma after surgical resection is favorable, recurrence has been reported in literature.
