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자료유형
학술저널
저자정보
Kim Min Hye (Department of Pediatrics Seoul National University Children’s Hospital Seoul Korea) Cho Myung Hyun (Department of Pediatrics Hallym University Sacred Heart Hospital Anyang Korea) Ahn Yo Han (Department of Pediatrics Seoul National University Children’s Hospital Seoul Korea) Bae Jeong Mo (Department of Pathology Seoul National University College of Medicine Seoul Korea) Moon Jin Soo (Department of Pediatrics Seoul National University Children’s Hospital Seoul Korea) Kang Hee Gyung (College of Medicine and Seoul National University Children’s Hospital)
저널정보
대한이식학회 Clinical Transplantation and Research Korean Journal of Transplantation Vol.35 No.4
발행연도
2021.12
수록면
262 - 267 (6page)
DOI
10.4285/kjt.21.0017

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Atypical hemolytic uremic syndrome (aHUS) is a rare disease caused by complement dysregulation that may involve the extra-renal system. Without appropriate prophylactic treatment, aHUS commonly recur after kidney transplantation (KT). In contrast, cytomegalovirus (CMV) infection is common in KT recipients and may affect various organ systems. Herein, we report a case of recurrent aHUS complicated by CMV enteritis. This 17-year-old KT recipient with aHUS having a CFH mutation was admitted to the hospital for gastric pain and vomiting. With worsening hemogram, recurrence of aHUS involving the gastrointestinal (GI) system was suspected. Upon treatment with anti-C5 antibody, the patient’s blood counts soon improved, but her GI symptoms did not. Esophagogastroduodenoscopy revealed multiple ulcers in the duodenum with pathologic findings consistent with aHUS and CMV enteritis; however, she did not have CMV antigenemia despite these findings. Treatment with ganciclovir resolved GI symptoms within 7 days. This case shows that recurrence of aHUS is often induced by intercurrent infection, and common infections after allograft transplantation, such as CMV, should always be suspected and confirmed for a proper treatment, particularly because CMV enteritis may not accompany CMV antigenemia.

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