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Rare Case of Congenital Thrombotic Thrombocytopenic Purpura Presenting as Posttransplant Thrombotic Microangiopathy

Title: Rare Case of Congenital Thrombotic Thrombocytopenic Purpura Presenting as Posttransplant Thrombotic Microangiopathy
Authors: Akila Viswanathan; Vidyashankar Panchangam; Shashank Shetty; Govardhan Reddy; Sanjeev S. Tonshal; Prakash Doraiswamy; M. R. Shashank; Kiran Krishne Gowda; Parameswaran Anoop
Source: Indian Journal of Transplantation, Vol 18, Iss 4, Pp 453-455 (2024)
Publisher Information: Wolters Kluwer Medknow Publications, 2024.
Publication Year: 2024
Collection: LCC:Surgery
Subject Terms: plasmapheresis; posttransplant; thrombotic microangiopathy; Surgery; RD1-811
Description: Middle-aged female underwent transplantation with her mother as a donor after appropriate desensitization. The patient developed graft dysfunction with systemic features of thrombotic microangiopathy. Renal allograft biopsy was suggestive of antibody-mediated rejection. She was treated with plasmapheresis followed by intravenous immunoglobulin. However, due to lack of response, further workup was sent and the patient was found to have ADAMTS 13 levels
Document Type: article
File Description: electronic resource
Language: English
ISSN: 2212-0017; 2212-0025
Relation: https://journals.lww.com/10.4103/ijot.ijot_29_24; https://doaj.org/toc/2212-0017; https://doaj.org/toc/2212-0025
DOI: 10.4103/ijot.ijot_29_24
Access URL: https://doaj.org/article/7fc69dfd026346ba8d0833360e9acd3d
Accession Number: edsdoj.7fc69dfd026346ba8d0833360e9acd3d
Database: Directory of Open Access Journals