Abstract
Central diabetes insipidus (DI) is a rare complication in patients with acute myeloid leukemia (AML), typically occurring in patients with abnormalities of chromosomes 3 or 7. The association between AML with monosomy 7 and DI has been described in a number of studies; however, DI has been rarely reported in cases of ectopic virus integration site‑1 (EVI1)‑positive AML with monosomy 7. The current study reports a case of AML with monosomy 7 and EVI1 overexpression, with central DI as the initial symptom. The patient was an 18‑year‑old female who presented with polyuria and polydipsia. Bone marrow aspiration revealed 83.5% myeloperoxidase‑positive blasts without trilineage myelodysplasia. The karyotype was 45,XX,‑7, and the patient presented monosomy 7 and EVI1 overexpression (‑7/EVI1+) without 3q aberration. Treatment with induction therapy was unsuccessful. To the best of our knowledge, this is the second case of DI‑AML with ‑7/EVI1+ and without a 3q aberration. The possible mechanisms associated with EVI1, monosomy 7 and DI were investigated.
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Ma, H., Yang, J., Xiang, B., & Jia, Y. (2015). Acute myeloid leukemia with monosomy 7, ectopic virus integration site-1 overexpression and central diabetes insipidus: A case report. Oncology Letters, 9(6), 2459–2462. https://doi.org/10.3892/ol.2015.3139
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