Kim Ho Hyun, Park Eun Kyu, Seoung Jin Shick, Hur Young Hoe, Koh Yang Seok, Kim Jung Chul, Cho Chol Kyoon, Kim Hyun Jong
Division of Hepato-Biliary-Pancreatic Surgery, Department of Surgery, Chonnam National University Medical School, Gwangju, Korea.
J Korean Surg Soc. 2011 Jun;80 Suppl 1(Suppl 1):S55-8. doi: 10.4174/jkss.2011.80.Suppl1.S55. Epub 2011 Jun 17.
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.
淋巴管瘤是一种罕见的先天性良性肿瘤,起源于淋巴系统,多见于小儿患者的颈部和腋窝区域(95%)。胰腺淋巴管瘤极为罕见,占这些肿瘤的比例不到1%。我们在此报告一例胰腺囊性淋巴管瘤。一名54岁女性出现间歇性餐后腹部不适并伴有背部放射痛。腹部计算机断层扫描显示胰腺尾部有一个8×6.5厘米的低密度囊性肿块,无分隔或实性成分。初步诊断为胰腺假性囊肿。患者接受了远端胰腺切除术加脾切除术。组织病理学和免疫组织化学研究有助于诊断胰腺囊性淋巴管瘤。在此,我们报告一例酷似胰腺假性囊肿的胰腺囊性淋巴管瘤病例,并复习相关医学文献。