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Atypical hemolytic uremic syndrome during induction chemotherapy in neuroblastoma, a rare phenomenon or common congenital predisposition?

  • Meghan Davitt
  • , Rachel Offenbacher
  • , Michelle A. Lee
  • , David M. Loeb
  • , Deepa Manwani
  • , William Mitchell
  • , Daniel A. Weiser
    • Montefiore Health System

    Research output: Contribution to journal › Article › peer-review

    1 Scopus citations

    Abstract

    Atypical hemolytic uremic syndrome (aHUS) is a complement-mediated thrombotic microangiopathy sometimes associated with germline variants in genes of the complement system. Clinical findings of microangiopathic hemolytic anemia, thrombocytopenia, and acute kidney injury arise due to aberrant complement protein activation in the circulation. A 13-month-old boy with metastatic neuroblastoma (NB) developed aHUS during his first cycle of induction chemotherapy with germline testing revealing a complement factor H (CFH) gene mutation, currently classified as a variant of uncertain significance (VUS). Now he is in disease remission after successful complement blockade therapy, thus highlighting a unique presentation of aHUS in a patient with newly diagnosed NB.

    Original languageEnglish
    Article numbere31175
    Pages (from-to)e31175
    JournalPediatric Blood and Cancer
    Volume71
    Issue number9
    DOIs
    StatePublished - Sep 2024

    Keywords

    • Antineoplastic Combined Chemotherapy Protocols/adverse effects
    • Atypical Hemolytic Uremic Syndrome/drug therapy
    • Complement Factor H/genetics
    • Germ-Line Mutation
    • Humans
    • Induction Chemotherapy/adverse effects
    • Infant
    • Male
    • Neuroblastoma/drug therapy

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