超声内镜引导下细针穿刺诊断11岁男童胰腺囊性淋巴管瘤1例

IF 0.2 Q4 GASTROENTEROLOGY & HEPATOLOGY International Journal of Hepatobiliary and Pancreatic Diseases Pub Date : 2016-12-23 DOI:10.5348/IJHPD-2016-64-CR-20
Qian Chen, Yun Wang, Jinglin Wang, W. Hou, B. Zou, Bin Cheng
{"title":"超声内镜引导下细针穿刺诊断11岁男童胰腺囊性淋巴管瘤1例","authors":"Qian Chen, Yun Wang, Jinglin Wang, W. Hou, B. Zou, Bin Cheng","doi":"10.5348/IJHPD-2016-64-CR-20","DOIUrl":null,"url":null,"abstract":"\n \n Introduction: Pancreatic cystic lymphangioma (PCL) is an extremely rare benign tumor of lymphatic origin. Traditionally, it is diagnosed at surgery performed on a patient with a retroperitoneal cyst of unclear etiology. However, recently a few single case reports showed PCL was successfully diagnosed by endoscopic ultrasound with fine-needle aspiration (EUS-FNA).\n Case Report: We present a new case of PCL in an 11-year-old boy who came to our hospital for swelling of the body. A contrast-enhanced computed tomography scan revealed a 7.7×4.5 cm cystic lesion involving head and neck of the pancreas. EUS-FNA was subsequently performed and diagnosis of PCL was made based on result of cytological examination and measurement of aspirate.\n Conclusion: In agreement with previous reports, we show that EUS-FNA confirmed the cystic lesion in pancreas and further provided the gross, biochemical and cytological features supporting accurate diagnosis of PCL.\n","PeriodicalId":40532,"journal":{"name":"International Journal of Hepatobiliary and Pancreatic Diseases","volume":"1 1","pages":""},"PeriodicalIF":0.2000,"publicationDate":"2016-12-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Diagnosis of pancreatic cystic lymphangioma in an 11-year-old boy with endoscopic ultrasound-guided fine needle aspiration: A case report\",\"authors\":\"Qian Chen, Yun Wang, Jinglin Wang, W. Hou, B. Zou, Bin Cheng\",\"doi\":\"10.5348/IJHPD-2016-64-CR-20\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"\\n \\n Introduction: Pancreatic cystic lymphangioma (PCL) is an extremely rare benign tumor of lymphatic origin. Traditionally, it is diagnosed at surgery performed on a patient with a retroperitoneal cyst of unclear etiology. However, recently a few single case reports showed PCL was successfully diagnosed by endoscopic ultrasound with fine-needle aspiration (EUS-FNA).\\n Case Report: We present a new case of PCL in an 11-year-old boy who came to our hospital for swelling of the body. A contrast-enhanced computed tomography scan revealed a 7.7×4.5 cm cystic lesion involving head and neck of the pancreas. EUS-FNA was subsequently performed and diagnosis of PCL was made based on result of cytological examination and measurement of aspirate.\\n Conclusion: In agreement with previous reports, we show that EUS-FNA confirmed the cystic lesion in pancreas and further provided the gross, biochemical and cytological features supporting accurate diagnosis of PCL.\\n\",\"PeriodicalId\":40532,\"journal\":{\"name\":\"International Journal of Hepatobiliary and Pancreatic Diseases\",\"volume\":\"1 1\",\"pages\":\"\"},\"PeriodicalIF\":0.2000,\"publicationDate\":\"2016-12-23\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"International Journal of Hepatobiliary and Pancreatic Diseases\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.5348/IJHPD-2016-64-CR-20\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"GASTROENTEROLOGY & HEPATOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Journal of Hepatobiliary and Pancreatic Diseases","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.5348/IJHPD-2016-64-CR-20","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"GASTROENTEROLOGY & HEPATOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

简介:胰腺囊性淋巴管瘤是一种极其罕见的淋巴源性良性肿瘤。传统上,它是在手术中诊断的病人腹膜后囊肿病因不明。然而,最近的一些个案报告显示,PCL是成功诊断的内镜超声细针抽吸(EUS-FNA)。病例报告:我们提出一个新的病例PCL在一个11岁的男孩谁来到我们医院肿胀的身体。增强计算机断层扫描显示7.7×4.5厘米囊性病变累及胰腺头颈部。随后行EUS-FNA检查,根据细胞学检查结果和抽吸量测定诊断PCL。结论:与以往报道一致,EUS-FNA证实了胰腺囊性病变,并进一步提供了支持PCL准确诊断的大体、生化和细胞学特征。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Diagnosis of pancreatic cystic lymphangioma in an 11-year-old boy with endoscopic ultrasound-guided fine needle aspiration: A case report
Introduction: Pancreatic cystic lymphangioma (PCL) is an extremely rare benign tumor of lymphatic origin. Traditionally, it is diagnosed at surgery performed on a patient with a retroperitoneal cyst of unclear etiology. However, recently a few single case reports showed PCL was successfully diagnosed by endoscopic ultrasound with fine-needle aspiration (EUS-FNA). Case Report: We present a new case of PCL in an 11-year-old boy who came to our hospital for swelling of the body. A contrast-enhanced computed tomography scan revealed a 7.7×4.5 cm cystic lesion involving head and neck of the pancreas. EUS-FNA was subsequently performed and diagnosis of PCL was made based on result of cytological examination and measurement of aspirate. Conclusion: In agreement with previous reports, we show that EUS-FNA confirmed the cystic lesion in pancreas and further provided the gross, biochemical and cytological features supporting accurate diagnosis of PCL.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
2
期刊最新文献
A unique presentation of peliosis hepatis: A case report and comprehensive review of the literature Multicenter retrospective cohort study: Using trends in liver function tests to predict spontaneous passage of common bile duct stones in choledocholithiasis Multicenter retrospective cohort study: Using trends in liver function tests to predict spontaneous passage of common bile duct stones in choledocholithiasis IgG4-related inflammatory pseudotumor of the liver presenting as an incidental solitary liver mass Bile duct injury in laparoscopic cholecystectomy with a posterior infundibular approach
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1