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Pediatric secondary CML in a patient with HLH carrying UNC13D , LYST and ITK variant
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  • chengshuang huang,
  • Pei Huang,
  • Xi Luo,
  • Zhixu He,
  • YAN CHEN
chengshuang huang
Affiliated Hospital of Zunyi Medical University

Corresponding Author:[email protected]

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Pei Huang
Affiliated Hospital of Zunyi Medical University
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Xi Luo
Affiliated Hospital of Zunyi Medical University
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Zhixu He
Affiliated Hospital of Zunyi Medical University
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YAN CHEN
Affiliated Hospital of Zunyi Medical University
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Abstract

Hemophagocytic lymphohistiocytosis (HLH) is a rare, life-threatening disease. This case report describes a secondary chronic myelogenous leukemia (CML) in a nine-year-old male after treatment with a combination of etoposide (VP16), steroids and cyclosporin for HLH. VP16 can potentially induce leukemia, and single nucleotide polymorphisms may be involved in the pathogenesis of CML. We speculate that genetic backgrounds combined with chemotherapeutic drugs lead to secondary CML. This case report alerts physicians to the importance of genetic screening and the rare side effects of VP16 in children with HLH.