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Polychondritis terminating in Eosinophilic Leukemia

  • Case Report
  • Published:
Pathology & Oncology Research

Abstract

We report here on a patient presenting with Relapsing Polychondritis (RP) two years before the diagnosis of Myelodysplasia (MDS) terminating in Eosinophilic Leukemia (EoL). The evolution of RP several years prior to the presentation of MDS does not support a paraneoplastic etiology of RP in this patient. The terminal development of EoL in our case is assumed to represent clonal evolution caused by a second mutagenic event. The existence of autoimmune skin disorders in both the patient and his offspring (vitiligo and subacute cutaneous lupus erythematosus, respectively) implies that the coexistence of MDS and RP may have been caused by a functional disturbance of the immune system.

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VÁrkonyi, J., Jakab, L., Zalatnay, A. et al. Polychondritis terminating in Eosinophilic Leukemia. Pathol. Oncol. Res. 3, 135–138 (1997). https://doi.org/10.1007/BF02907809

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  • DOI: https://doi.org/10.1007/BF02907809

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