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Conclusion                                         10.  Tsai H. Advances in the pathogenesis, diagnosis, and treat-
                                                                      ment of thrombotic thrombocytopenic purpura.  J Am Soc
               TMA syndromes represent a group of disorders defined   Nephrol. 2003;14:1072–1081.
               by shared characteristics of microangiopathic hemo-  11.  Veyradier A, Obert B, Houllier A, et al. Specific von Will-
               lytic anemia, thrombocytopenia, and organ injury from   ebrand factor cleaving protease in thrombotic microangio-
                                                                      pathies: a study of 111 cases. Blood 2001;98:1765–1772.
               pathologic small-vessel thrombosis.  Evaluation and   12.  Vesely SK, George JN, Lämmle B, et al. ADAMTS13 activity
               management in the field require astute clinical judg-  in thrombotic thrombocytopenic  purpura-hemolytic uremic
               ment and empiric supportive treatment until evacuation   syndrome: relation to presenting features and clinical out-
               occurs. In the hospital setting, empiric treatment with   comes in a prospective cohort of 142 patients. Blood. 2003;
               plasma exchange is critical because of the significant   102:60–68.
               reduction in morbidity and mortality in treatment of   13.  Cataland S, Wu H. How I treat: the clinical differentiation
                                                                      and initial treatment of adult patients with atypical hemolytic
               TTP. Laboratory testing is then pursued to differentiate   uremic syndrome. Blood. 2014;123:2478–2484.
               the TMA syndromes. TTP is often associated with an   14.  Legendre CM, Licht C, Muus P, et al. Terminal complement
               ADAMTS13 deficiency. HUS usually occurs in the pres-   inhibitor eculizumab in atypical hemolytic-uremic syndrome.
               ence of Shiga toxin. In the absence of these syndromes,   N Engl J Med. 2013;368:2169–2181.
               advanced laboratory testing must be pursued to define
               a specific TMA syndrome, which may have a different
               treatment, prognosis, and long-term management.    LT Croom, MC, USN, is currently an Undersea Medical Of-
                                                                  ficer assigned to the Naval Special Warfare Center, San  Diego,
                                                                  California. He previously was stationed at Naval Medical
               Acknowledgment
                                                                  Center San Diego, where he completed internship in internal
                                                                  medicine. He is a graduate of the Uniformed Services Univer-
               This case was presented in a poster at the Navy chapter   sity of the Health Sciences. E-mail: daniel.croom@socom.mil.
               of the American College of Physicians annual confer-
               ence at the Walter Reed National Military Medical Cen-  CDR Tracy, MC, USN, is with the Department of Hematol-
               ter, Bethesda, Maryland, on 4 December 2015.       ogy Oncology, Naval Medical Center San Diego, California.


               Disclosures
               The authors have indicated they have no financial rela-
               tionship relevant to this article to disclose.             Association of Police Officer
                                                                        Paramedics of the United States

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