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      Central diabetes insipidus and partial anterior pituitary dysfunction in acute myeloid leukemia

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          Abstract

          Summary

          Central diabetes insipidus (CDI) is a rare manifestation of acute myeloid leukemia (AML) with unclear etiology. When present, CDI in AML has most often been described in patients with chromosome 3 or 7 aberrations and no abnormalities on brain imaging. In this case, we present a woman with newly diagnosed AML t(12;14)(p12;q13) found to have diabetes insipidus (DI) with partial anterior pituitary dysfunction and abnormal brain imaging. While in hospital, the patient developed an elevated serum sodium of 151 mmol/L with a serum osmolality of 323 mmol/kg and urine osmolality of 154 mmol/kg. On history, she reported polyuria and polydipsia for 5 months preceding hospitalization. Based on her clinical symptoms and biochemistry, she was diagnosed with DI and treated using intravenous desmopressin with good effect; sodium improved to 144 mmol/L with a serum osmolality of 302 mmol/kg and urine osmolality of 501 mmol/kg. An MRI of the brain done for the assessment of neurologic involvement revealed symmetric high-T2 signal within the hypothalamus extending into the mamillary bodies bilaterally, a partially empty sella, and loss of the pituitary bright spot. A pituitary panel was completed which suggested partial anterior pituitary dysfunction. The patient’s robust improvement with low-dose desmopressin therapy along with her imaging findings indicated a central rather than nephrogenic cause for her DI. Given the time course of her presentation with respect to her AML diagnosis, MRI findings, and investigations excluding other causes, her CDI and partial anterior pituitary dysfunction were suspected to be secondary to hypothalamic leukemic infiltration.

          Learning points
          • Leukemic infiltration of the pituitary gland is a rare cause of central diabetes insipidus (CDI) in patients with acute myeloid leukemia (AML).

          • Patients with AML and CDI may compensate for polyuria and prevent hypernatremia with increased water intake.

          • AML-associated CDI can require long-term desmopressin treatment, independent of AML response to treatment.

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          Most cited references9

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          Diabetes insipidus

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            Acute myeloid leukemia with central diabetes insipidus

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              Monosomy 7 predisposes to diabetes insipidus in leukaemia and myelodysplastic syndrome.

              We studied the chromosomes in the bone marrow of 4 patients who had both diabetes insipidus (DI) and acute non-lymphocytic leukaemia. Clinical findings suggested that, in each case, myelodysplastic syndrome had preceded the onset of acute leukaemia. Two other such patients described in the literature had had a banded karyotype study of bone marrow cells. All 6 patients had deletions of chromosome 7. 3 had monosomy 7 as the sole cytogenetic abnormality, 2 had monosomy 7 associated with other clonal abnormalities and 1 had del(7)(q22) in association with other abnormalities. These data suggest that monosomy 7 or perhaps monosomy for 7q22-qter predisposes to DI. The mechanism by which the proposed predisposition is produced remains to be clarified.

                Author and article information

                Journal
                Endocrinol Diabetes Metab Case Rep
                Endocrinol Diabetes Metab Case Rep
                EDM
                Endocrinology, Diabetes & Metabolism Case Reports
                Bioscientifica Ltd (Bristol )
                2052-0573
                27 June 2022
                2022
                : 2022
                : 21-0153
                Affiliations
                [1 ]Department of Medicine , University of Toronto, Toronto, Ontario, Canada
                [2 ]Division of Endocrinology and Metabolism , Department of Medicine, University of Toronto, Toronto, Ontario, Canada
                [3 ]Banting and Best Diabetes Centre , University Health Network, University of Toronto, Toronto, Ontario, Canada
                Author notes
                Correspondence should be addressed to R Arya; Email: rigya.arya@ 123456mail.utoronto.ca
                Author information
                http://orcid.org/0000-0003-0762-6148
                Article
                EDM210153
                10.1530/EDM-21-0153
                9346312
                01d9c7d9-13f6-4e13-bf4a-08991b5f4621
                © The authors

                This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License..

                History
                : 30 May 2022
                : 27 June 2022
                Categories
                Geriatric
                Female
                White
                Canada
                Hypothalamus
                Pituitary
                Pituitary
                Haematology
                Insight into Disease Pathogenesis or Mechanism of Therapy
                Insight into Disease Pathogenesis or Mechanism of Therapy

                geriatric,female,white,canada,hypothalamus,pituitary,haematology,insight into disease pathogenesis or mechanism of therapy,july,2022

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