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Transformation of CMML to AML presenting with acute kidney injury

Characterized by bone marrow dysplasia and peripheral blood monocytosis, chronic myelomonocytic leukemia (CMML) is one of the most aggressive chronic leukemias and has a propensity for progression to acute myeloid leukemia (AML). Patients with newly diagnosed AML generally present with symptoms rela...

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Autores principales: DeBoer, Rebecca, Garrahy, Ian, Rettew, Andrew, Libera, Robert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7427458/
https://www.ncbi.nlm.nih.gov/pubmed/32850097
http://dx.doi.org/10.1080/20009666.2020.1774271
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author DeBoer, Rebecca
Garrahy, Ian
Rettew, Andrew
Libera, Robert
author_facet DeBoer, Rebecca
Garrahy, Ian
Rettew, Andrew
Libera, Robert
author_sort DeBoer, Rebecca
collection PubMed
description Characterized by bone marrow dysplasia and peripheral blood monocytosis, chronic myelomonocytic leukemia (CMML) is one of the most aggressive chronic leukemias and has a propensity for progression to acute myeloid leukemia (AML). Patients with newly diagnosed AML generally present with symptoms related to complications of pancytopenia but can also present with renal insufficiency. We present a 79-year-old male with a past medical history of CMML and chronic kidney disease stage 3 (baseline creatinine 1.8 mg/dL) who presented with one day of inability to urinate and 20-lb unintentional weight loss, fatigue, and bone pain over 3 months. Laboratory evaluation revealed leukocytosis of 88.5 x 10(3)/uL (normal 4.8–10.8 x 10(3)/uL) with 24.0% monocytes on differential, creatinine 2.94 mg/dL (baseline creatinine 1.7–1.9 mg/dL), uric acid 19.8 mg/dL, potassium 4.0 mmol/L, phosphorus 4.0 mg/dL, calcium 9.2 mg/dL, and albumin 3.2 g/dL. Urinalysis was significant for protein 200 mg/dL, 20/LPF granular casts, and 7/LPF hyaline casts. Bone marrow biopsy revealed 20–30% blasts with monocytic features of differentiation consistent with acute myeloid leukemia. Computed tomography (CT) of the abdomen and pelvis appreciated splenomegaly with retroperitoneal, and pelvic lymphadenopathy. Kidney failure can complicate the presentation of AML but can be rapidly reversible with treatment. In patients with CMML who have progressive renal insufficiency and hyperuricemia, there should be a high index of suspicion for progression to AML.
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spelling pubmed-74274582020-08-25 Transformation of CMML to AML presenting with acute kidney injury DeBoer, Rebecca Garrahy, Ian Rettew, Andrew Libera, Robert J Community Hosp Intern Med Perspect Case Report Characterized by bone marrow dysplasia and peripheral blood monocytosis, chronic myelomonocytic leukemia (CMML) is one of the most aggressive chronic leukemias and has a propensity for progression to acute myeloid leukemia (AML). Patients with newly diagnosed AML generally present with symptoms related to complications of pancytopenia but can also present with renal insufficiency. We present a 79-year-old male with a past medical history of CMML and chronic kidney disease stage 3 (baseline creatinine 1.8 mg/dL) who presented with one day of inability to urinate and 20-lb unintentional weight loss, fatigue, and bone pain over 3 months. Laboratory evaluation revealed leukocytosis of 88.5 x 10(3)/uL (normal 4.8–10.8 x 10(3)/uL) with 24.0% monocytes on differential, creatinine 2.94 mg/dL (baseline creatinine 1.7–1.9 mg/dL), uric acid 19.8 mg/dL, potassium 4.0 mmol/L, phosphorus 4.0 mg/dL, calcium 9.2 mg/dL, and albumin 3.2 g/dL. Urinalysis was significant for protein 200 mg/dL, 20/LPF granular casts, and 7/LPF hyaline casts. Bone marrow biopsy revealed 20–30% blasts with monocytic features of differentiation consistent with acute myeloid leukemia. Computed tomography (CT) of the abdomen and pelvis appreciated splenomegaly with retroperitoneal, and pelvic lymphadenopathy. Kidney failure can complicate the presentation of AML but can be rapidly reversible with treatment. In patients with CMML who have progressive renal insufficiency and hyperuricemia, there should be a high index of suspicion for progression to AML. Taylor & Francis 2020-08-02 /pmc/articles/PMC7427458/ /pubmed/32850097 http://dx.doi.org/10.1080/20009666.2020.1774271 Text en © 2020 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group on behalf of Greater Baltimore Medical Center. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
DeBoer, Rebecca
Garrahy, Ian
Rettew, Andrew
Libera, Robert
Transformation of CMML to AML presenting with acute kidney injury
title Transformation of CMML to AML presenting with acute kidney injury
title_full Transformation of CMML to AML presenting with acute kidney injury
title_fullStr Transformation of CMML to AML presenting with acute kidney injury
title_full_unstemmed Transformation of CMML to AML presenting with acute kidney injury
title_short Transformation of CMML to AML presenting with acute kidney injury
title_sort transformation of cmml to aml presenting with acute kidney injury
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7427458/
https://www.ncbi.nlm.nih.gov/pubmed/32850097
http://dx.doi.org/10.1080/20009666.2020.1774271
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