Thrombotic microangiopathy after kidney transplantation: Expanding etiologic and pathogenetic spectra

doi:10.5500/wjt.v14.i1.90277

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Mar 18, 2024 (publication date) through Mar 10, 2025

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World Journal of Transplantation

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2220-3230

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Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA

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World J Transplant. Mar 18, 2024; 14(1): 90277
Published online Mar 18, 2024. doi: 10.5500/wjt.v14.i1.90277

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Figure 4 An algorithmic approach to diagnosis, classification and treatment of posttransplant thrombotic microangiopathy. ADAMTS13: A disintegrin-like and metalloprotease with thrombospondin type 1 motif, 13; AMR: Antibody-mediated rejection; IMS: Immunosuppression; LDH: Lactate dehydrogenase; MCP: Membrane cofactor protein; PT-TMA: Posttransplant thrombotic microangiopathy; SPEP: Serum protein electrophoresis; TMA: Thrombotic microangiopathy; UPEP: Urine protein electrophoresis; VUS: Variant of unknown significance.

Citation: Mubarak M, Raza A, Rashid R, Sapna F, Shakeel S. Thrombotic microangiopathy after kidney transplantation: Expanding etiologic and pathogenetic spectra. World J Transplant 2024; 14(1): 90277
URL: https://www.wjgnet.com/2220-3230/full/v14/i1/90277.htm
DOI: https://dx.doi.org/10.5500/wjt.v14.i1.90277