| Literature DB >> 22066085 |
Ho Hyun Kim1, Eun Kyu Park, Jin Shick Seoung, Young Hoe Hur, Yang Seok Koh, Jung Chul Kim, Chol Kyoon Cho, Hyun Jong Kim.
Abstract
Lymphangiomas are rare congenital benign tumors arising from the lymphatic system, and are mostly encountered in the neck and axillary regions of pediatric patients (95%). Lymphangioma of the pancreas is extremely rare accounting for less than 1% of these tumors. We report here on a case of pancreatic cystic lymphangioma. A 54-year-old woman presented with intermittent postprandial abdominal discomfort and radiating back pain. Abdominal computed tomography scan revealed 8 × 6.5 cm hypodense cystic mass arising from the tail of the pancreas without septa or solid component. The initial impression was a pancreatic pseudocyst. The patient underwent distal pancreatectomy with splenectomy. The histopathologic and immunohistochemical study helped make the diagnosis of a pancreatic cystic lymphangioma. Herein, we report a case of pancreatic cystic lymphangioma mimicking pancreatic pseudocyst and review the relevant medical literature.Entities:
Keywords: Cystic lymphangioma; Pancreas; Pseudocyst; Surgical excision
Year: 2011 PMID: 22066085 PMCID: PMC3205361 DOI: 10.4174/jkss.2011.80.Suppl1.S55
Source DB: PubMed Journal: J Korean Surg Soc ISSN: 1226-0053