移植相关卡波西氏肉瘤的肾脏移植:1例报告。

Jae Jun Lee, Jin-Myung Kim, Youngmin Ko, Hye Eun Kwon, Joo Hee Jung, Hyunwook Kwon, Young Hoon Kim, Sung Shin
{"title":"移植相关卡波西氏肉瘤的肾脏移植:1例报告。","authors":"Jae Jun Lee,&nbsp;Jin-Myung Kim,&nbsp;Youngmin Ko,&nbsp;Hye Eun Kwon,&nbsp;Joo Hee Jung,&nbsp;Hyunwook Kwon,&nbsp;Young Hoon Kim,&nbsp;Sung Shin","doi":"10.4285/kjt.23.0001","DOIUrl":null,"url":null,"abstract":"<p><p>Kaposi's sarcoma (KS) is a disease that is not widely known among the general public, but has a high prevalence among organ transplant recipients. Here, we present a rare case of intragraft KS after kidney transplantation. A 53-year-old woman who had been on hemodialysis due to diabetic nephropathy underwent deceased-donor kidney transplantation on December 7, 2021. Approximately 10 weeks after kidney transplantation, her creatinine level increased to 2.99 mg/dL. Upon examination, ureter kinking was confirmed between the ureter orifices and the transplanted kidney. As a result, percutaneous nephrostomy was performed, and a ureteral stent was inserted. During the procedure, bleeding occurred due to a renal artery branch injury, and embolization was performed immediately. Subsequently, kidney necrosis and uncontrolled fever developed, leading to graftectomy. Surgical findings revealed that the kidney parenchyma was necrotic as a whole, and lymphoproliferative lesions had formed diffusely around the iliac artery. These lesions were removed during graftectomy, and a histological examination was performed. The kidney graft and lymphoproliferative lesions were diagnosed as KS based on a histological examination. We report a rare case in which a recipient developed KS in the kidney allograft as well as in adjacent lymph nodes.</p>","PeriodicalId":33357,"journal":{"name":"Korean Journal of Transplantation","volume":"37 2","pages":"135-140"},"PeriodicalIF":0.0000,"publicationDate":"2023-06-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/63/bb/kjt-37-2-135.PMC10332279.pdf","citationCount":"0","resultStr":"{\"title\":\"Transplant-associated Kaposi's sarcoma in a kidney allograft: a case report.\",\"authors\":\"Jae Jun Lee,&nbsp;Jin-Myung Kim,&nbsp;Youngmin Ko,&nbsp;Hye Eun Kwon,&nbsp;Joo Hee Jung,&nbsp;Hyunwook Kwon,&nbsp;Young Hoon Kim,&nbsp;Sung Shin\",\"doi\":\"10.4285/kjt.23.0001\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Kaposi's sarcoma (KS) is a disease that is not widely known among the general public, but has a high prevalence among organ transplant recipients. Here, we present a rare case of intragraft KS after kidney transplantation. A 53-year-old woman who had been on hemodialysis due to diabetic nephropathy underwent deceased-donor kidney transplantation on December 7, 2021. Approximately 10 weeks after kidney transplantation, her creatinine level increased to 2.99 mg/dL. Upon examination, ureter kinking was confirmed between the ureter orifices and the transplanted kidney. As a result, percutaneous nephrostomy was performed, and a ureteral stent was inserted. During the procedure, bleeding occurred due to a renal artery branch injury, and embolization was performed immediately. Subsequently, kidney necrosis and uncontrolled fever developed, leading to graftectomy. Surgical findings revealed that the kidney parenchyma was necrotic as a whole, and lymphoproliferative lesions had formed diffusely around the iliac artery. These lesions were removed during graftectomy, and a histological examination was performed. The kidney graft and lymphoproliferative lesions were diagnosed as KS based on a histological examination. We report a rare case in which a recipient developed KS in the kidney allograft as well as in adjacent lymph nodes.</p>\",\"PeriodicalId\":33357,\"journal\":{\"name\":\"Korean Journal of Transplantation\",\"volume\":\"37 2\",\"pages\":\"135-140\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2023-06-30\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/63/bb/kjt-37-2-135.PMC10332279.pdf\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Korean Journal of Transplantation\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.4285/kjt.23.0001\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"Medicine\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Korean Journal of Transplantation","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4285/kjt.23.0001","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 0

摘要

卡波西肉瘤(KS)是一种在普通公众中并不广为人知的疾病,但在器官移植受者中发病率很高。在此,我们报告一例罕见的肾移植后体内KS。一名因糖尿病肾病接受血液透析的53岁女性于2021年12月7日接受了已故供者肾移植。肾移植后约10周,她的肌酐水平上升至2.99 mg/dL。经检查,确认输尿管口与移植肾之间有输尿管扭结。结果,经皮肾造口术,并插入输尿管支架。在手术过程中,由于肾动脉分支损伤导致出血,立即进行了栓塞术。随后出现肾坏死和不受控制的发热,导致移植物切除术。手术结果显示肾实质整体坏死,髂动脉周围弥漫淋巴增生性病变。这些病变在移植物切除术中被移除,并进行组织学检查。根据组织学检查,肾移植和淋巴增生性病变被诊断为KS。我们报告一个罕见的情况下,受者发展KS在肾移植以及邻近的淋巴结。
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
Transplant-associated Kaposi's sarcoma in a kidney allograft: a case report.

Kaposi's sarcoma (KS) is a disease that is not widely known among the general public, but has a high prevalence among organ transplant recipients. Here, we present a rare case of intragraft KS after kidney transplantation. A 53-year-old woman who had been on hemodialysis due to diabetic nephropathy underwent deceased-donor kidney transplantation on December 7, 2021. Approximately 10 weeks after kidney transplantation, her creatinine level increased to 2.99 mg/dL. Upon examination, ureter kinking was confirmed between the ureter orifices and the transplanted kidney. As a result, percutaneous nephrostomy was performed, and a ureteral stent was inserted. During the procedure, bleeding occurred due to a renal artery branch injury, and embolization was performed immediately. Subsequently, kidney necrosis and uncontrolled fever developed, leading to graftectomy. Surgical findings revealed that the kidney parenchyma was necrotic as a whole, and lymphoproliferative lesions had formed diffusely around the iliac artery. These lesions were removed during graftectomy, and a histological examination was performed. The kidney graft and lymphoproliferative lesions were diagnosed as KS based on a histological examination. We report a rare case in which a recipient developed KS in the kidney allograft as well as in adjacent lymph nodes.

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
Korean Journal of Transplantation
Korean Journal of Transplantation Medicine-Transplantation
CiteScore
0.80
自引率
0.00%
发文量
32
审稿时长
24 weeks
期刊最新文献
Inferior polar nephrectomy and vesicocalicostomy for complete ureteric stricture following antibody-mediated rejection in ABO-incompatible living donor kidney transplant: a report of a rare case. Overcoming the longest cold ischemia time yet seen in Korea using hypothermic machine perfusion in deceased donor kidney transplantation: a case report. Patient management for thoracic organ donor candidates: the lung transplantation team's view. Surgical techniques for robotic right donor hepatectomy, part 2: robotic parenchymal transection and bile duct division. Surgical techniques for robotic right donor hepatectomy, part 1: robotic hilar dissection and right lobe mobilization.
×
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