H. Kim, S. Han, H. Park, Hyun-woo Kim, R. Hong, N. Choi, M. Shin, N. Yoon, Hyun Lee Kim, J. Chung, B. Shin
{"title":"Successful Treatment of Invasive Gastric Mucormycosis in a Kidney Transplant Recipient","authors":"H. Kim, S. Han, H. Park, Hyun-woo Kim, R. Hong, N. Choi, M. Shin, N. Yoon, Hyun Lee Kim, J. Chung, B. Shin","doi":"10.4285/JKSTN.2018.32.4.104","DOIUrl":null,"url":null,"abstract":"Type : Poster Presentation No. : PTL 031 Successful treatment of invasive gastric mucormycosis in kidney transplant recipient Hyun Woo Kim, Ha Yeol Park, Hyun Lee Kim, Jong Hoon Chung, Byung Chul Shin Department of Internal Medicine-Nephrology, Chosun University Hospital, Korea, Republic of Case Study: Mucormycosis is an extremely rare, but potentially life-threatening fungal infection. Gastrointestinal (GI) mucormycosis is rare and occurs primarily in the extremely malnourished patients especially infants or children. A 55-year-old man with end-stage renal disease due to diabetic nephropathy underwent deceased donor kidney transplantation on 2years ago. He complained of abdominal pain and distension on 3days ago at admission. A computed tomography (CT) scan revealed diffuse gastric wall thickening. A gastrointestinal (GI) endoscopy showed huge grey colored elevated necrotic debris surrounded by erythematous erosive mucosa at antrum to upper body. Microscopic examination obtained from a GI endoscopic specimen demonstrated peptic detritus with numerous nonseptate mucor hyphae was noted in the mucosa and submucosa. Mucormycosis was diagnosed according to the clinical findings and morphological features. A total gastrectomy was performed and antifungal agent was supplied. Microscopic examination obtained from a surgical specimen demonstrated invasive mucormycosis with numerous fungal hyphae with invasion into mucosa to subserosa. The patient and graft successfully treated to the infection with total gastrectomy and antifungal therapy. GI endocscopy showed gastric mucormycosis","PeriodicalId":420886,"journal":{"name":"The Journal of The Korean Society for Transplantation","volume":"89 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2018-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Journal of The Korean Society for Transplantation","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4285/JKSTN.2018.32.4.104","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1
Abstract
Type : Poster Presentation No. : PTL 031 Successful treatment of invasive gastric mucormycosis in kidney transplant recipient Hyun Woo Kim, Ha Yeol Park, Hyun Lee Kim, Jong Hoon Chung, Byung Chul Shin Department of Internal Medicine-Nephrology, Chosun University Hospital, Korea, Republic of Case Study: Mucormycosis is an extremely rare, but potentially life-threatening fungal infection. Gastrointestinal (GI) mucormycosis is rare and occurs primarily in the extremely malnourished patients especially infants or children. A 55-year-old man with end-stage renal disease due to diabetic nephropathy underwent deceased donor kidney transplantation on 2years ago. He complained of abdominal pain and distension on 3days ago at admission. A computed tomography (CT) scan revealed diffuse gastric wall thickening. A gastrointestinal (GI) endoscopy showed huge grey colored elevated necrotic debris surrounded by erythematous erosive mucosa at antrum to upper body. Microscopic examination obtained from a GI endoscopic specimen demonstrated peptic detritus with numerous nonseptate mucor hyphae was noted in the mucosa and submucosa. Mucormycosis was diagnosed according to the clinical findings and morphological features. A total gastrectomy was performed and antifungal agent was supplied. Microscopic examination obtained from a surgical specimen demonstrated invasive mucormycosis with numerous fungal hyphae with invasion into mucosa to subserosa. The patient and graft successfully treated to the infection with total gastrectomy and antifungal therapy. GI endocscopy showed gastric mucormycosis