Warm-antibody autoimmune hemolytic anemia developing after thrombotic thrombocytopenic purpura

Daniel Morgensztern, Mohamed A. Kharfan-Dabaja, Han Mou Tsai, Eric C.Y. Lian

Research output: Contribution to journalArticlepeer-review

9 Scopus citations


Thrombotic thrombocytopenic purpura (TTP) and warm-antibody autoimmune hemolytic anemia (AIHA) are uncommon diseases. Although TTP has been increasingly described in association with autoimmune antibodies, there are very few reports of the association with autoimmune hematological conditions, including idiopathic thrombocytopenic purpura and AIHA. Here we describe a patient with classic manifestations of TTP, who was successfully treated with plasma exchange. A few weeks later, she developed warm-antibody AIHA, which responded promptly to prednisone.

Original languageEnglish
Pages (from-to)154-156
Number of pages3
JournalActa Haematologica
Issue number3
StatePublished - Nov 23 2002


  • Autoimmune hemolytic anemia
  • Evans' syndrome
  • Thrombotic thrombocytopenic purpura


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