A Rare Case of Microgranular Acute Promyelocytic Leukemia Associated with ider(17)(q10)t(15;17) in an Old-age Patient

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참고문헌 (18)

1. Swerdlow SH, "WHO classification of tumours of haematopoietic and lymphoid tissues. 4th ed", pp.112~114 (2008), IARC
2. Lengfelder E, "Treatment concepts of acute promyelocytic leukemia", Crit Rev Oncol Hematol, 56, pp.261~274 (2005)
3. Sirulnik LA, "Acute promyelocytic leukemia: current strategies for the treatment of newly diagnosed disease", Clin Adv Hematol Oncol, 3, pp.391~429 (2005)
4. Xu L, "Molecular cytogenetic characterization and clinical relevance of additional, complex and", or variant chromosome abnormalities in acute promyelocytic leukemia, 2001, pp.15, 1359~1368
5. Hiorns LR, "Additional chromosome abnormalities confer worse prognosis in acute promyelocytic leukaemia", Br J Haematol, 96, pp.314~321 (1997)
6. Cervera J, "Additional chromosome abnormalities in patients with acute promyelocytic leukemia treated with all-trans retinoic acid and chemotherapy", Haematologica, 95, pp.424~431 (2010)
7. Hernández JM, "Additional cytogenetic changes do not influence the outcome of patients with newly diagnosed acute promyelocytic leukemia treated with an ATRA plus anthracyclin based protocol. A report of the Spanish group PETHEMA", Haematologica, 86, pp.807~813 (2001)
8. Chou WC, "Clinical and biological characteristics of acute promyelocytic leukemia in Taiwan: a high relapse rate in patients with high initial and peak white blood cell counts during all-trans retinoic acid treatment", Leukemia, 11, pp.921~928 (1997)
9. Kaleem Z, "Acute promyelocytic leukemia with additional chromosomal abnormalities and absence of Auer rods", Am J Clin Pathol, 112, pp.113~118 (1999)
10. Manola KN, "Isochromosome der(17)(q10)t(15;17) in acute promyelocytic leukemia resulting in an additional copy of the RARA-PML fusion gene: report of 4 cases and review of the literature", Acta Haematol, 123, pp.162~170 (2010)
11. Kim M, "Two distinct clonal populations in acute promyelocytic leukemia, one involving chromosome 17 and the other involving an isochromosome 17", CANCER GENETICS AND CYTOGENETICS, 197, pp.185~188 (2010), ELSEVIER
12. Sainty D, "A new morphologic classification system for acute promyelocytic leukemia distinguishes cases with underlying PLZF", RARA gene rearrangements. Group Français de Cytogénétique Hématologique, UK Cancer Cytogenetics Group and BIOMED 1 European Coomunity-Concerted Acion “Molecular Cytogenetic Diagnosis in Haematological Malignancies.”, 2000, pp.96, 1287~1296
13. Kim MJ, "ider(17)(q10)t(15;17) associated with relapse and poor prognosis in a pediatric patient with acute promyelocytic leukemia", CANCER GENETICS AND CYTOGENETICS, 201(2), pp.116~121 (2010), elsevier
14. Simmers RN, "Localization of the G-CSF gene on chromosome 17 proximal to the breakpoint in the t(15;17) in acute promyelocytic leukemia", Blood, 70, pp.330~332 (1987)
15. Prigogina EL, "Chromosomes in acute nonlymphocytic leukemia", Hum Genet, 73, pp.137~146 (1986)
16. Schoch C, "Incidence and implication of additional chromosome aberrations in acute promyelocytic leukaemia with translocation t(15;17)(q22;q21): a report on 50 patients", Br J Haematol, 94, pp.493~500 (1996)
17. Qiu HR, "Clinical and laboratory studies of an acute promyelocytic leukemia patient with double ider(17q) chromosome aberration", Cancer Genet Cytogenet, 184, pp.74~75 (2008)
18. Kim MJ, "ABL1 gene deletion without BCR", ABL1 rearrangement in a young adolescent with precursor B-cell acute lymphoblastic leukemia: clinical study and literature review, 2010, pp.196(2), 184~188[DOI]

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