Thrombotic microangiopathy in acute kidney injury: Diagnostic and therapeutic challenges in a literature review
DOI:
https://doi.org/10.33448/rsd-v15i1.50572Keywords:
Thrombotic Microangiopathies, Acute Kidney Injury, Review Literature.Abstract
Thrombotic Microangiopathy (TMA) is an uncommon and life-threatening condition characterized by microangiopathic hemolytic anemia, thrombocytopenia, and endothelial injury, frequently associated with acute kidney injury (AKI). Early recognition remains clinically challenging due to overlapping manifestations with other nephrological and hematological disorders, as well as limited access to confirmatory diagnostic tests. This study aimed to critically analyze the available evidence regarding the main diagnostic and therapeutic challenges of TMA associated with AKI. This is a narrative literature review with a descriptive and qualitative approach. The literature search was conducted in November 2025 in the PubMed and LILACS databases using MeSH terms related to thrombotic microangiopathy, acute kidney injury, diagnosis, and treatment, combined with Boolean operators. Studies published between 2015 and 2025 in Portuguese, English, and Spanish were included, encompassing clinical guidelines, clinical trials, meta-analyses, reviews, and observational studies. The analyzed studies demonstrate relevant advances in the understanding of TMA pathophysiology, particularly regarding the role of the complement system and the use of biomarkers and genetic testing to refine diagnostic accuracy. Clinical benefits were observed with the early initiation of targeted therapies, such as plasma exchange and complement inhibitors, with favorable impact on morbidity, mortality, and preservation of renal function. In conclusion, timely identification and a multidisciplinary approach are essential to optimize clinical management and improve patient outcomes.
References
Bianchi, L., Palone, F., Vitali, R., De Angelis, P., & Cucchiara, S. (2018). Síndrome hemolítico-urêmica: Diagnóstico diferencial com o início de sintomas inflamatórios intestinais. Acta Bio Medica Atenei Parmensis, 89(Suppl. 9), 79–82. https://doi.org/10.23750/abm.v89i9-S.7911
Booth, K. K., Terrell, D. R., Vesely, S. K., & George, J. N. (2011). Systemic infections mimicking thrombotic thrombocytopenic purpura. American Journal of Hematology, 86(10), 743–751. https://doi.org/10.1002/ajh.22091
Brocklebank, V., Wood, K. M., & Kavanagh, D. (2018). Microangiopathy and the kidney. Clinical Journal of the American Society of Nephrology, 13(2), 300–317. https://doi.org/10.2215/CJN.00620117
Casarin, S. T., Porto, A. R., Gabatz, R. I. B., Bonow, C. A., Ribeiro, J. P. & Mota, M. S. (2020). Tipos de revisão de literatura. Journal of Nursing and Health.J. nurs. health. 10(n.esp.):e20104031.
Coelho Júnior, J. L., Farias, J. S. H., Araújo, N. C., Queiroz, R. M., Silva, L. S., & Daher, E. F. (2021). Thrombotic microangiopathy associated with arboviral infection: Report of three cases. PLoS Neglected Tropical Diseases, 15(10), e0009790. https://doi.org/10.1371/journal.pntd.0009790
Dong, G., Chen, J., Liu, Y., Gao, J., Chen, Y., Wang, Z., & Huang, S. (2024). Acute kidney injury associated with thrombotic microangiopathy: Characterization, prevalence, and prognosis. Medicine, 103(25), e39431. https://doi.org/10.1097/MD.0000000000039431
Farias, J. S. H., Daher, E. F., Marques, C. N., Menezes, F. R., Lima, L. L., & Mota, R. M. S. (2016). Renal recovery in atypical hemolytic uremic syndrome treated with eculizumab. Jornal Brasileiro de Nefrologia, 38(1), 137–141. https://doi.org/10.5935/0101-2800.20160021
Fenandes, J. M. B., Vieira, L. T. & Castelhano, M. V. C. (2023). Revisão narrativa enquanto metodologia científica significativa: reflexões técnico-formativas. REDES – Revista Educacional da Sucesso. 3(1), 1-7. ISSN: 2763-6704.
Gil, A. C. (2017). Como elaborar um projeto de pesquisa. Editora Atlas.
Hanna, R., Gibney, R., & Boysen-Osborn, M. (2025). Thrombotic microangiopathies. Emergency Medicine Clinics of North America, 43(3), 407–420. https://doi.org/10.1016/j.emc.2025.03.008
Java, A., Burwick, R., & Chang, A. (2024). Thrombotic microangiopathies and the kidney. Advances in Chronic Kidney Disease, 31(3), 255–264. https://doi.org/10.1053/j.ackd.2023.09.003
Joffre, J., Roux, S., Vardon-Bounes, F., Boyer, M., Chenevier-Gobeaux, C., Planquette, B., Azoulay, E., Darmon, M., & Galanaud, J.‑P. (2023). Reversible cutaneous microvascular hyporeactivity in immune-mediated thrombotic thrombocytopenic purpura. Critical Care, 27(1), 328. https://doi.org/10.1186/s13054-023-04405-w
Kaname, S., Miura, S., Matsumoto, M., Uemura, M., Isonishi, A., Kato, S., & Fujimura, Y. (2024). Outcomes in patients with trigger-associated thrombotic microangiopathy after plasma exchange: A systematic review. Transfusion and Apheresis Science, 63(1), 104048. https://doi.org/10.1016/j.transci.2024.104048
Martins, J. I. S., Barreto, A. G. M., Neto, M. C., Barros, R. T., & Sabbaga, E. (2019). Renal histological findings in a patient with acute renal injury associated with purpura fulminans: A case report. Jornal Brasileiro de Nefrologia, 41(2), 296–299. https://doi.org/10.1590/2175-8239-JBN-2018-0090
McFarlane, P. A., Kim, S. J., Robinson, L. A., McCaw, R., Hou, S., Copland, M., & Scholey, J. (2021). Making the correct diagnosis in thrombotic microangiopathy: A narrative review. Therapeutic Advances in Rare Disease, 2, 1–18. https://doi.org/10.1177/2633004021108707
Moake, J. L. (2002). Thrombotic microangiopathies. The New England Journal of Medicine, 347(8), 589–600. https://doi.org/10.1056/NEJMra020528
Noris, M., & Remuzzi, G. (2009). Atypical hemolytic–uremic syndrome. The New England Journal of Medicine, 361(17), 1676–1687. https://doi.org/10.1056/NEJMra0902814
Pereira, A. S. et al. (2018). Metodologia da pesquisa científica. [free ebook]. Santa Maria. Editora da UFSM.
Pugh, D., Barlas, R. S., Kavanagh, D., & Bastin, A. J. (2021). Interventions for atypical haemolytic uraemic syndrome. Cochrane Database of Systematic Reviews, 2021(3), CD012862. https://doi.org/10.1002/14651858.CD012862.pub2
Rother, E. T. (2007). Revisão sistematica x revisão narrativa. Acta Paulista de Enfermagem. 20(2), 5-6.
Shen, Y. M. (2016). Clinical assessment of thrombotic microangiopathy: Identifying patients with suspected atypical hemolytic uremic syndrome. Thrombosis Journal, 14(Suppl. 1), 19. https://doi.org/10.1186/s12959-016-0114-0
Thoreau, B., Gay, J., Fakhouri, F., Presne, C., Fakhouri, R., & Frimat, L. (2022). Infection in patients with suspected thrombotic microangiopathy based on clinical presentation. Clinical Journal of the American Society of Nephrology, 17(1), 58–67. https://doi.org/10.2215/CJN.17511120
Tseng, M. H., Lin, J. J., Lee, C. Y., Tsai, I. J., Hsu, C. N., & Lin, Y. J. (2022). Atypical hemolytic uremic syndrome: Consensus on diagnosis and treatment in Taiwan. Journal of the Formosan Medical Association, 122(12), 1065–1076. https://doi.org/10.1016/j.jfma.2022.10.006
Vaisbich, M. H., Koch, V. H. K., Fujimura, M. D., & Sociedade Brasileira de Nefrologia. (2024). Recommendations for the diagnosis and treatment of atypical hemolytic uremic syndrome: Brazilian consensus. Jornal Brasileiro de Nefrologia, 46(4), e20240087. https://doi.org/10.1590/2175-8239-JBN-2024-0087
Van Doorn, D. P. C., Tobal, R., Abdul-Hamid, M. A., Van Paassen, P., & Timmermans, S. A. M. E. G. (2025). Etiology and outcomes of kidney-limited and systemic thrombotic microangiopathy. Modern Pathology, 38(4), 100690. https://doi.org/10.1016/j.modpat.2024.1
Downloads
Published
Issue
Section
License
Copyright (c) 2026 Vitória Florentino Santana, Márcia Cristina Coutinho Razuk Jorge, Raquel Luciana Angela Marques Tauro

This work is licensed under a Creative Commons Attribution 4.0 International License.
Authors who publish with this journal agree to the following terms:
1) Authors retain copyright and grant the journal right of first publication with the work simultaneously licensed under a Creative Commons Attribution License that allows others to share the work with an acknowledgement of the work's authorship and initial publication in this journal.
2) Authors are able to enter into separate, additional contractual arrangements for the non-exclusive distribution of the journal's published version of the work (e.g., post it to an institutional repository or publish it in a book), with an acknowledgement of its initial publication in this journal.
3) Authors are permitted and encouraged to post their work online (e.g., in institutional repositories or on their website) prior to and during the submission process, as it can lead to productive exchanges, as well as earlier and greater citation of published work.
