Multiple Myeloma as the Underlying Cause of Thrombotic Microangiopathy Leading to Acute Kidney Injury: Revisiting a Very Rare Entity

Savneek Chugh, Asim Kichloo, Firas Jafri, Liga Yusvirazi, Robert Lerner

Research output: Contribution to journalArticlepeer-review

4 Scopus citations

Abstract

Thrombotic microangiopathy (TMA) describes a pathological process of microvascular thrombosis, consumptive thrombocytopenia, and microangiopathic hemolytic anemia, leading to end-organ ischemia and infarction, affecting particularly the kidney and brain. TMA is a pathological feature of a number of clinical disorders including thrombotic thrombocytopenic purpura, hemolytic uremic syndrome, and atypical hemolytic uremic syndrome. Rare but important, TMA may also occur in malignancy, connective tissue disease, malignant hypertension, and renal transplantation (rejection or drug toxicity). We present a very rare case where the patient developed acute kidney injury from TMA but found to have multiple myeloma as the possible underlying etiology.

Original languageEnglish
JournalJournal of Investigative Medicine High Impact Case Reports
Volume5
Issue number3
DOIs
StatePublished - Sep 1 2017

Keywords

  • hemolytic uremic syndrome
  • microangiopathic hemolytic anemia
  • multiple myeloma
  • thrombotic microangiopathy
  • thrombotic thrombocytopenic purpura

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