Abstract

BackgroundThrombotic microangiopathy is caused by various conditions, but few cases secondary to trauma have been reported. We present the rare case of a patient with thrombotic microangiopathy-induced high-impact trauma with hemorrhagic shock.Case presentationAn 86-year-old Japanese woman was transferred to our hospital after a traffic accident. A whole-body computed tomography scan revealed pelvic fractures with massive extravasation. She received a blood transfusion and emergency angiographic embolization. On post-traumatic day 1, she showed unexplained severe hemolysis, thrombocytopenia, and renal failure despite her stable condition. Disseminated intravascular coagulation was excluded because her activated partial thromboplastin time and prothrombin time-international normalized ratio were normal. Her fragmented red blood cell concentration was 28.8%. We suspected clinical thrombotic thrombocytopenic purpura and started plasma exchange. She recovered fully after the plasma exchange and was discharged on day 31. We eventually diagnosed thrombotic microangiopathy because her ADAMTS13 activity was not reduced.ConclusionsIt is important to recognize the possibility that thrombotic microangiopathy may occur after severe trauma. In the critical care setting, unexplained thrombocytopenia and hemolytic anemia should be investigated to eliminate the possibility of thrombotic microangiopathy. Early plasma exchange may help to prevent unfortunate outcomes in patients with thrombotic microangiopathy following trauma.

Highlights

  • Thrombotic microangiopathy is caused by various conditions, but few cases secondary to trauma have been reported

  • It is important to recognize the possibility that thrombotic microangiopathy may occur after severe trauma

  • In the critical care setting, unexplained thrombocytopenia and hemolytic anemia should be investigated to eliminate the possibility of thrombotic microangiopathy

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Summary

Conclusions

In the critical care setting, unexplained thrombocytopenia and hemolytic anemia should be investigated to eliminate the possibility of TMA. Availability of data and materials Please contact author for data requests. All authors read and approved the final manuscript. Ethics approval and consent to participate This case report has been approved by the research ethics committee of our hospital. A copy of the written consent is available for review by the Editor-in-Chief of this journal. Author details 1The Department of Emergency and Critical Care Medicine, Niigata City General Hospital, 463-7 Shumoku, Chuo-ku, Niigata, Niigata 950-1197, Japan.

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