Athrombocytopenic thrombotic microangiopathy: diagnosis not performed with the present criteria

  • Lorenzo Marovelli Servicio de Nefrología, Sanatorio La Trinidad Mitre, Buenos Aires
  • Ignacio Larzábal Servicio de Nefrología, Sanatorio La Trinidad Mitre, Buenos Aires
  • Eugenia Zopi Servicio de Nefrología, Sanatorio La Trinidad Mitre, Buenos Aires
  • César Agost Carreño Servicio de Nefrología, Sanatorio La Trinidad Mitre, Buenos Aires
  • Martín Winkel Winkel Clínica Médica, Hospital General de Agudos Dr. Juan A. Fernández, Buenos Aires
  • Diana Miserendino Anatomía Patológica, Hospital General de Agudos José María Ramos Mejía, Buenos Aires
Keywords: athrombocytopenic thrombotic microangiopathy, thrombocytopenia, thrombotic thrombocytopenic purpura, hemolytic uremic syndrome, acute renal failure

Abstract

The disease category of thrombotic microangiopathy (TM) encompass different entities such as thrombocvtopenic thrombotic purpura (TTP) and uremic hemolytic syndrome (UHS), both strongly related and whose diagnosis relies on the presence of non immune hemolytic anemia and trombocytopenia, findings that should urge the caring physician to start plasmapheresis promptly. We report the case of a 51 year old woman admitted with acute-subacute renal failure of unknown etiology whose renal biopsy finding was thrombotic microangiopathy, in absence of thrombocytopenia and haemolytic anemia. This inusual case and according to published literature can not be diagnosed on standard accepted criteria and others markers like ADAMTS-13 should be considered.

References

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Published
2017-11-01
How to Cite
1.
Marovelli L, Larzábal I, Zopi E, Agost Carreño C, Winkel MW, Miserendino D. Athrombocytopenic thrombotic microangiopathy: diagnosis not performed with the present criteria. Rev Nefrol Dial Traspl. [Internet]. 2017Nov.1 [cited 2024Jul.16];32(1):47-0. Available from: http://revistarenal.org.ar/index.php/rndt/article/view/194
Section
Case Report