Suppr超能文献

酷似胰腺假性囊肿的胰腺囊性淋巴管瘤。

Cystic lymphangioma of the pancreas mimicking pancreatic pseudocyst.

作者信息

Kim Ho Hyun, Park Eun Kyu, Seoung Jin Shick, Hur Young Hoe, Koh Yang Seok, Kim Jung Chul, Cho Chol Kyoon, Kim Hyun Jong

机构信息

Division of Hepato-Biliary-Pancreatic Surgery, Department of Surgery, Chonnam National University Medical School, Gwangju, Korea.

出版信息

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.

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.

摘要

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。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验