신이식 환자의 폐에서 발생한 평활근종의
The overall incidence of malignancy in a renal transplanted patient is 3 to 5 times higher compared with general population. We report a very rare case of multiple leiomyoma originated from lung after renal transplantation. 33-year-old male underwent renal transplantation in November, 1989. A 5 mm s...
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Veröffentlicht in: | Kidney research and clinical practice 2003-11, Vol.22 (6), p.767 |
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creator | 유선진 Yu Seon Jin 정성진 Jeong Seong Jin 김일 Kim Il 박환철 Park Hwan Cheol 윤여욱 Yun Yeo Ug 이창화 Lee Chang Hwa 강경원 Kang Gyeong Won 강종명 Kang Jong Myeong 박문향 Park Mun Hyang |
description | The overall incidence of malignancy in a renal transplanted patient is 3 to 5 times higher compared with general population. We report a very rare case of multiple leiomyoma originated from lung after renal transplantation. 33-year-old male underwent renal transplantation in November, 1989. A 5 mm sized pulmonary nodule was found in the left lower lobe incidentally in March, 2001. The size of pulmonary nodule increased and same lesion was found on the opposite side of the lung on chest roentgenogram after one year, so we proceeded with computed tomography of the chest. Variable sized multiple nodules in the whole lung field were noted, which were thought be metastatic lesions, and for detection of the primary site of malignancy, further study including esophagogastroduodenoscope, colon study, abdominal ultrasound, abdominal CT, bone scan and tumor marker were checked, but there was no evidence of primary cancer. After open lung biopsy low malignant potential smooth muscle tumor was noted, and Epstein-barr virus (EBV) DNA was detected. The patient had been maintained on immunosuppressive therapy with cyclosporine and mycophenolate mofetil (MMF), and after the diagnosis of leiomyoma administration of MMF was stoped, and cyclosporine dosage was reduced. With the reduction of immunosuppressants, intravenous immunoglobulin trial was done for the first cycle, but the efficacy of treatment is not clear. (Korean J Nephrol 2003;22(6):767-772) |
format | Article |
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We report a very rare case of multiple leiomyoma originated from lung after renal transplantation. 33-year-old male underwent renal transplantation in November, 1989. A 5 mm sized pulmonary nodule was found in the left lower lobe incidentally in March, 2001. The size of pulmonary nodule increased and same lesion was found on the opposite side of the lung on chest roentgenogram after one year, so we proceeded with computed tomography of the chest. Variable sized multiple nodules in the whole lung field were noted, which were thought be metastatic lesions, and for detection of the primary site of malignancy, further study including esophagogastroduodenoscope, colon study, abdominal ultrasound, abdominal CT, bone scan and tumor marker were checked, but there was no evidence of primary cancer. After open lung biopsy low malignant potential smooth muscle tumor was noted, and Epstein-barr virus (EBV) DNA was detected. The patient had been maintained on immunosuppressive therapy with cyclosporine and mycophenolate mofetil (MMF), and after the diagnosis of leiomyoma administration of MMF was stoped, and cyclosporine dosage was reduced. With the reduction of immunosuppressants, intravenous immunoglobulin trial was done for the first cycle, but the efficacy of treatment is not clear. (Korean J Nephrol 2003;22(6):767-772)</description><identifier>ISSN: 2211-9132</identifier><language>kor</language><publisher>대한신장학회</publisher><subject>EBV ; Epstein-barr virus ; Immunosuppressants ; Renal transplantation ; Smooth muscle tumor</subject><ispartof>Kidney research and clinical practice, 2003-11, Vol.22 (6), p.767</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,781,785</link.rule.ids></links><search><creatorcontrib>유선진</creatorcontrib><creatorcontrib>Yu Seon Jin</creatorcontrib><creatorcontrib>정성진</creatorcontrib><creatorcontrib>Jeong Seong Jin</creatorcontrib><creatorcontrib>김일</creatorcontrib><creatorcontrib>Kim Il</creatorcontrib><creatorcontrib>박환철</creatorcontrib><creatorcontrib>Park Hwan Cheol</creatorcontrib><creatorcontrib>윤여욱</creatorcontrib><creatorcontrib>Yun Yeo Ug</creatorcontrib><creatorcontrib>이창화</creatorcontrib><creatorcontrib>Lee Chang Hwa</creatorcontrib><creatorcontrib>강경원</creatorcontrib><creatorcontrib>Kang Gyeong Won</creatorcontrib><creatorcontrib>강종명</creatorcontrib><creatorcontrib>Kang Jong Myeong</creatorcontrib><creatorcontrib>박문향</creatorcontrib><creatorcontrib>Park Mun Hyang</creatorcontrib><title>신이식 환자의 폐에서 발생한 평활근종의</title><title>Kidney research and clinical practice</title><addtitle>Kidney Research and Clinical Practice(구 대한신장학회지)</addtitle><description>The overall incidence of malignancy in a renal transplanted patient is 3 to 5 times higher compared with general population. We report a very rare case of multiple leiomyoma originated from lung after renal transplantation. 33-year-old male underwent renal transplantation in November, 1989. A 5 mm sized pulmonary nodule was found in the left lower lobe incidentally in March, 2001. The size of pulmonary nodule increased and same lesion was found on the opposite side of the lung on chest roentgenogram after one year, so we proceeded with computed tomography of the chest. Variable sized multiple nodules in the whole lung field were noted, which were thought be metastatic lesions, and for detection of the primary site of malignancy, further study including esophagogastroduodenoscope, colon study, abdominal ultrasound, abdominal CT, bone scan and tumor marker were checked, but there was no evidence of primary cancer. After open lung biopsy low malignant potential smooth muscle tumor was noted, and Epstein-barr virus (EBV) DNA was detected. The patient had been maintained on immunosuppressive therapy with cyclosporine and mycophenolate mofetil (MMF), and after the diagnosis of leiomyoma administration of MMF was stoped, and cyclosporine dosage was reduced. With the reduction of immunosuppressants, intravenous immunoglobulin trial was done for the first cycle, but the efficacy of treatment is not clear. (Korean J Nephrol 2003;22(6):767-772)</description><subject>EBV</subject><subject>Epstein-barr virus</subject><subject>Immunosuppressants</subject><subject>Renal transplantation</subject><subject>Smooth muscle tumor</subject><issn>2211-9132</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><recordid>eNpjYeA0MjI01LU0NDbiYOAtLs5MMjA1MDc2MbOw4GQwf9O94M3cLW-65yq8nTnjzbwJb-bOUHjbP-HN9AlvWuYovN4w503z3LdT5wDFOt_OnPNq-543i1qBangYWNMSc4pTeaE0N4O0m2uIs4dudmZxcXxBUWZuYlFlvJGhgaGBibkxflkAPXRAAw</recordid><startdate>20031130</startdate><enddate>20031130</enddate><creator>유선진</creator><creator>Yu Seon Jin</creator><creator>정성진</creator><creator>Jeong Seong Jin</creator><creator>김일</creator><creator>Kim Il</creator><creator>박환철</creator><creator>Park Hwan Cheol</creator><creator>윤여욱</creator><creator>Yun Yeo Ug</creator><creator>이창화</creator><creator>Lee Chang Hwa</creator><creator>강경원</creator><creator>Kang Gyeong Won</creator><creator>강종명</creator><creator>Kang Jong Myeong</creator><creator>박문향</creator><creator>Park Mun Hyang</creator><general>대한신장학회</general><scope>HZB</scope><scope>Q5X</scope></search><sort><creationdate>20031130</creationdate><title>신이식 환자의 폐에서 발생한 평활근종의</title><author>유선진 ; Yu Seon Jin ; 정성진 ; Jeong Seong Jin ; 김일 ; Kim Il ; 박환철 ; Park Hwan Cheol ; 윤여욱 ; Yun Yeo Ug ; 이창화 ; Lee Chang Hwa ; 강경원 ; Kang Gyeong Won ; 강종명 ; Kang Jong Myeong ; 박문향 ; Park Mun Hyang</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-kiss_primary_21010473</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>kor</language><creationdate>2003</creationdate><topic>EBV</topic><topic>Epstein-barr virus</topic><topic>Immunosuppressants</topic><topic>Renal transplantation</topic><topic>Smooth muscle tumor</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>유선진</creatorcontrib><creatorcontrib>Yu Seon Jin</creatorcontrib><creatorcontrib>정성진</creatorcontrib><creatorcontrib>Jeong Seong Jin</creatorcontrib><creatorcontrib>김일</creatorcontrib><creatorcontrib>Kim Il</creatorcontrib><creatorcontrib>박환철</creatorcontrib><creatorcontrib>Park Hwan Cheol</creatorcontrib><creatorcontrib>윤여욱</creatorcontrib><creatorcontrib>Yun Yeo Ug</creatorcontrib><creatorcontrib>이창화</creatorcontrib><creatorcontrib>Lee Chang Hwa</creatorcontrib><creatorcontrib>강경원</creatorcontrib><creatorcontrib>Kang Gyeong Won</creatorcontrib><creatorcontrib>강종명</creatorcontrib><creatorcontrib>Kang Jong Myeong</creatorcontrib><creatorcontrib>박문향</creatorcontrib><creatorcontrib>Park Mun Hyang</creatorcontrib><collection>Korean Studies Information Service System (KISS)</collection><collection>Korean Studies Information Service System (KISS) B-Type</collection><jtitle>Kidney research and clinical practice</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>유선진</au><au>Yu Seon Jin</au><au>정성진</au><au>Jeong Seong Jin</au><au>김일</au><au>Kim Il</au><au>박환철</au><au>Park Hwan Cheol</au><au>윤여욱</au><au>Yun Yeo Ug</au><au>이창화</au><au>Lee Chang Hwa</au><au>강경원</au><au>Kang Gyeong Won</au><au>강종명</au><au>Kang Jong Myeong</au><au>박문향</au><au>Park Mun Hyang</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>신이식 환자의 폐에서 발생한 평활근종의</atitle><jtitle>Kidney research and clinical practice</jtitle><addtitle>Kidney Research and Clinical Practice(구 대한신장학회지)</addtitle><date>2003-11-30</date><risdate>2003</risdate><volume>22</volume><issue>6</issue><spage>767</spage><pages>767-</pages><issn>2211-9132</issn><abstract>The overall incidence of malignancy in a renal transplanted patient is 3 to 5 times higher compared with general population. We report a very rare case of multiple leiomyoma originated from lung after renal transplantation. 33-year-old male underwent renal transplantation in November, 1989. A 5 mm sized pulmonary nodule was found in the left lower lobe incidentally in March, 2001. The size of pulmonary nodule increased and same lesion was found on the opposite side of the lung on chest roentgenogram after one year, so we proceeded with computed tomography of the chest. Variable sized multiple nodules in the whole lung field were noted, which were thought be metastatic lesions, and for detection of the primary site of malignancy, further study including esophagogastroduodenoscope, colon study, abdominal ultrasound, abdominal CT, bone scan and tumor marker were checked, but there was no evidence of primary cancer. After open lung biopsy low malignant potential smooth muscle tumor was noted, and Epstein-barr virus (EBV) DNA was detected. The patient had been maintained on immunosuppressive therapy with cyclosporine and mycophenolate mofetil (MMF), and after the diagnosis of leiomyoma administration of MMF was stoped, and cyclosporine dosage was reduced. With the reduction of immunosuppressants, intravenous immunoglobulin trial was done for the first cycle, but the efficacy of treatment is not clear. (Korean J Nephrol 2003;22(6):767-772)</abstract><pub>대한신장학회</pub><tpages>6</tpages></addata></record> |
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ispartof | Kidney research and clinical practice, 2003-11, Vol.22 (6), p.767 |
issn | 2211-9132 |
language | kor |
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source | DOAJ Directory of Open Access Journals |
subjects | EBV Epstein-barr virus Immunosuppressants Renal transplantation Smooth muscle tumor |
title | 신이식 환자의 폐에서 발생한 평활근종의 |
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