Secondary Acute Myeloid Leukemia after Polycythemia Vera: A Case Report

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Somchai Insiripong
Watcharin Yingsitsiri
Juree Boondumrongsagoon

Abstract

          Secondary acute myeloid leukemia (AML) can be found as the complication of polycythemiavera (PV) itself or the association with chemotherapy particularly hydroxyurea (HU). Herein we report a caseof 52-year old Thai woman who was diagnosed as PV based on the combination of the erythrocytosis, leukocytosis, thrombocytosis, huge splenomegaly and normal oxygen saturation. She has been treated with continual HU with occasional phlebotomy for nine years. The dose of HU has been adjusted according to the white blood cell count. Finally she develops chronic fever, weight loss, anemia, marked leukocytosis with predominant blasts in the peripheral blood and recurrent huge splenomegaly. The definite diagnosis of secondary AML after PV can be made by the bone marrow immunophenotyping and positive JAK2 mutation. She is treated with the combination of cytosine arabinoside and idarubicin regimen and she can tolerate it well. With this case report, the association of the incident of AML after PV and HU therapy is discussed.

Article Details

How to Cite
Insiripong, S. . ., Yingsitsiri, W. ., & Boondumrongsagoon, J. . (2024). Secondary Acute Myeloid Leukemia after Polycythemia Vera: A Case Report . Maharat Nakhon Ratchasima Hospital Journal, 38(2), 123–126. Retrieved from https://he04.tci-thaijo.org/index.php/MNRHJ/article/view/1592
Section
Case Report

References

Tefferi A. Polycythemia vera and essential throm bocythemia: 2012 update on diagnosis, risk

stratification, and management.Am J Hematol 2012;87:285-93.

Tefferi A, Rumi E, Finazzi G, Gisslinger H, Vannucchi AM, Rodeghiero F, et al. Chronic myeloproliferativeneoplasias: Survival and prognosis among 1545 patients with contemporary polycythemia vera: an international study. Leukemia 2013; 27:1874-81.

Nielsen I, Hasselbalch HC. Acute leukemia and myelodysplasia in patients with a Philadelphia

chromosome negative chronic myeloproliferative disorder treated with hydroxyurea alone or with hydroxyurea after busulphan. Am J Hematol 2003; 74: 26-31.

Fruchtman SM. Treatment paradigms in the management of myeloproliferative disorders. SeminHematol 2004; 41 (2 Suppl 3):18-22.

Sirhan S, Fairbanks VF, Tefferi A. Red cell mass and plasma volume measurements in polycythemia: evaluation of performance and practicalutility. Cancer 2005; 104: 213-5.

Tefferi A. Diagnostic approach to the patient with suspected polycythemia vera. In: UpToDate, Basow DS (Ed), UpToDate, Waltham, MA, 2008.

Camo´s M, Cervantes F, Montoto S,Herna´NdezBoluda JC, Villamor N,Montserrat E. Acute lymphoid leukemia following polycythemia vera. Leukemia & Lymphoma 1999; 32: 395-8.

Sonbol MB, BelalFirwana, Zarzour A, Morad M, Rana V, Tiu RV. Comprehensive review of JAK inhibitors in myeloproliferative neoplasms. TherAdvHematol 2013; 4: 15-35.

Finazzi G, Caruso V, Marchioli R, Capnist G, Chisesi T, Finelli C, et al. Acute leukemia in polycythemia vera: an analysis of 1638 patients enrolled in a prospective observational study. Blood 2005;105:2664-70.

Sterkers Y, Preudhomme C, Lai J-L, Demory J-L, Caulier M-T, E Wattel E, et al. Acute myeloid leukemia and myelodyslastic syndromes following essential thrombocythemia treated with hydroxyurea: high proportion of cases with 17p deletion. Blood 1998; 91:616-22.

Finazzi G, Barbui T. Hydroxyurea: the comparator in studies with new anti-JAK2 inhibitors. Hematology Meeting Reports 2009; 3: 108-14.

Swolin B, RÖdjer S, Westin J.Therapy-related patterns of cytogenetic abnormalities in acute myeloid leukemia and myelodysplastic syndrome post polycythemia vera: single center experience and review of literature. Ann Hematol 2008; 87: 467-74.