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Recipient-derived EBV-positive Monomorphic Plasmacytoma Type Posttransplant Lymphoproliferative Disorder After Allogeneic Stem Cell Transplant for Severe Aplastic Anemia: A Case Report.

作者信息

Carden Marcus A, Caltharp Shelley, Yee Marianne E, Haight Ann E, Westblade Lars F, Park Sunita

机构信息

*Aflac Cancer and Blood Disorders Center ‡Department of Pathology, Children's Healthcare of Atlanta †Department of Pediatrics, Emory University School of Medicine, Atlanta, GA §Department of Pathology and Laboratory Medicine, Weill Cornell Medical College, New York, NY.

出版信息

J Pediatr Hematol Oncol. 2016 Nov;38(8):e310-e314. doi: 10.1097/MPH.0000000000000613.

DOI:10.1097/MPH.0000000000000613
PMID:27403771
Abstract

Monomorphic plasmacytoma-type posttransplant lymphoproliferative disorder (PTLD) has not been reported after pediatric hematopoietic stem cell transplantation. We present a child with hepatitis-associated severe aplastic anemia who underwent an unrelated allogeneic hematopoietic stem cell transplantation and subsequently developed graft failure and an Epstein-Barr virus-positive monomorphic plasmacytoma-type PTLD of recipient origin. Despite broad-spectrum antimicrobials, weaning immunosuppression, rituximab administration, and a stem cell boost she died from complications of PTLD and a fungal pulmonary infection on day +78.

摘要

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