Chronic myeloid leukemia (CML) is one of the most common hematologic malignancies and accounts for 15% of all cases of leukemia in adults (1). The incidence of CML is approximately 1.6/100,000. The cytogenetic marker of the disease is the presence of a distinctive Philadelphia chromosome (Ph) in more than 95% of the patients (2). It is a reciprocal translocation between the long arms of chromosomes 9 and 22. The translocation involves the transfer of the Abelson or ABL1 gene on chromosome 9 to the breakpoint cluster region, BCR, of chromosome 22, resulting in a fusion BCR/ABL gene. The fusion gene produces BCR/ABL, a tyrosine kinase with deregulated activity that plays a key role in the development of CML.

Our case is an 83-year old woman who is directed to the genetic laboratory for a cytogenetic and molecular-genetic analysis suspected to be Ph positive [(+)]. Her initial diagnosis is primary aplastic anemia with additional diagnosis of primary (essential) hypertonia. The anamnesis is taken both from medical documentation and the statements of patient's relatives. She is accepted for the first time in the clinic having leukocytosis with neutrophilia, moderate-to-severe anemic syndrome-microcytic, hypochromic anemia; the thrombocytes are in the reference ranges. She has a consuming syndrome accompanied with a preserved and/or increased appetite and sore throat. Fever and feverish night sweats are lacking, there is no bleeding.

High levels of leucocytes have been diagnosed February, 2018. The leucocyte numbers increase in the following several months up to 85G/l. The levels from March, 2005 are documented as follows: St 12%; Sg 17%; Мо 2%; Ly 10%; Eo 5%; Bl + ProM 25%; M 21%; Meta M 9%.

Upon her acceptance in the hematological ward she is adequate and orientated. Her skin and mucosal membranes are pale pink with isolated suffusions and hematomas; no icterus is present. Peripheral lymph nodes are not enlarged on palpation; breathing is clear vesicular, double-sided, without wheezing. Cardiovascular system-there is arrhythmic cardiac activity, clear tones, systolic noise at Ao and cardiac apex. Stomach-soft, painless; liver-1-2 cm below the ribs' arch; spleen-non-enlarged. There are no swellings of the limbs.

At the Clinic of Hematology the patient is subjected to routine diagnostic procedures: Whole blood count test and biochemical analysis (Table I), morphological analysis of the blood cells, restriction analysis for V617F in JAK2 gene (Fig. 1), quantitative molecular-biological analysis (Real-time PCR) at the time of her first visit and three months after treatment (Fig. 2), and karyotyping (Fig. 3). For all procedures and tests the patient has provided a written informed consent.

The morphological analysis of cells' populations shows hypercellular bone marrow with an altered ratio between the neutrophil, granulocyte and erythroblast clones up to 12.1:1 (granulocytes 0.90; erythroblasts 0.07); hyperplasia of the neutrophil population with sustained maturation, increase of myelocytes and promyelocytes. Index of maturation 1.3 (reference values 0.5–0.8). Cytological features of gigantism in a part of the metamyelocytes. Substantially reduced erythroblast population with single representatives of all maturation forms. Well-presented megakaryocyte apparatus with a dominating population of polyploidic granulated megakaryocytes. The conclusion of the morphological analysis is ‘Chronic myeloproliferative process’. The ratio of different cell populations in the bone marrow is as follows: 1.5% lymphocytes, 87.9% granulocytes, 0.1% myeloblasts, 6.2% mature monocytes, 4.2% promonocytes. The whole blood count test of the patient and the biochemical analysis result at the time of her acceptance in the haematological ward of ‘St. Ivan Rilski’ Hospital is presented in Table I.

Based on the myelography the patient is directed for molecular-biological analysis for JAK2 mutation and Ph chromosome. The result of the restriction analysis is presented in Fig. 1 showing the genotype status of the patient (homozygous carrier of two wild type alleles for V617F JAK2 gene mutation).

Quantitative Real-time PCR analysis of the patient is performed (May, 2018) to confirm the presence of the molecular marker of CML-fusion gene BCR/ABL. The graph clearly shows the positive result of the amplification for both ABL (endogenous control) and BCR-ABL genes. The software estimates automatically the level of the fusion gene of 120% (IS) on the International Standardized Scale (Fig. 2A). Real-time analysis is performed second time (September, 2018) after four months' treatment with Tasigna (Nilotinitib) to monitor the molecular improvement of the patient. The result demonstrates 0,0019% (IS) (Fig. 2B) level which is much less compared to the patient's earlier data.

Karyotyping is performed after 24-h cultivation time of stimulated bone marrow specimen. Chromosomes are obtained, stained following Giemsa standard protocol and subsequently analyzed under light microscope (5). The cytogenetic analysis shows two different clones of cells: Hyperdiploid with additional chromosomes 8, 10 and 12 and Ph chromosome; and second clone which is Ph(+) with no hyperdiploidy (Fig. 3).

Hyperdiploidy is a phenomenon of having additional chromosomes rather than the diploid chromosome number in the karyotype. According to Onodera et al, hyperdiploid karyotype arises by a simultaneous gain of multiple chromosomes from a diploid karyotype during a single abnormal cell division (6). Generally hyperdiploidy is not a common event in CML patients (7). Other chromosome changes, such as chromosomal translocations, are more common, especially at the time of blast transformation (8). Hyperdiploidy could be a bad prognostic factor in CML (7,9). Further investigation on the topic shows that the existing statements about hyperdiploidy are ambiguous.

A case report (10) presents a Ph(+) CML case with hyperdiploidic karyotype and an additional T315I kinase domain (KD) mutation in the BCR-ABL gene. The patient responded well after therapy with Nilotinib. Though T315I mutation remained after the treatment, targeted drug eliminated the hyperdiploid clone (10).

In a study on acute lymphoblastic leukemia (ALL) in children high hyperdiploidy is characterized by a favourable prognosis (11). A paper studying chromosomal aberrations in pediatric and adult ALL defines high hyperdiploidy as present in 25–30% of children with favorable prognosis and 7–8% in adults with favorable/intermediate prognostic value (12). In multiple myeloma patients hypоdiploidy but not hyperdiploidy, is a poor indicator for the disease's development (13). According to some authors (14–16) hypodiploid DNA content is related to a poor response to chemotherapy and a very short survival time; according to others (17) hyperdiploid karyotype is associated with a better prognosis. The chromosomes which usually appear in addition in ALL karyotypes are 21, X, 14, 6, 18, 4, 17 and 10 which tend to be gained in blasts (18). The acquisition of chromosome 21 is seen in 95% of hyperdiploid cases.

There are only few reports about hyperdiploid karyotypes in CML cases. Rojas et al analyzes 63 cases with CML and not even one additional chromosome is found (19). There is only one case with i(17q); and one case with 21q deletion (19). Roland and Blahey reported a case of a patient with breast cancer who developed hyperdiploidy at the accelerated phase of the disease, near blast crisis, presenting with seven additional chromosomes besides Ph chromosome (+6, +8, +11, +18, +19, +20, +21) (8). Gains of chromosomes 6 and 19 are common in CML hyperdiploic karyotypes (8). Other commonly reported chromosomes are 8 and 19 in Ph(+) cases of CML (20). In a study of 256 patients with CML only one is with 51 chromosomes and trisomy +6, +10, +13 and +19 (21). Chromosomes +7, +8, +9, +10, +12, +15, +19 are reported in a case with near triploid karyotype in pre-imatinib mesylate CML patient with T315I mutation in BCR-ABL kinase domain (10).

The reported case in this study has been diagnosed as CML as for of an absence of a blast infiltration in the bone marrow. The myelogram and the immunophenotyping characteristics of the cells reveal the percentage of myeloblasts in the bone marrow estimated at 0.1%. Besides being Ph(+), the patient shows a hyperdiploid karyotype with additional chromosomes 8, 10 and 12 (see ‘Results’). To our knowledge, this is the only report of chromosome 12 in a hyperdiploid CML patient.

The underlying mechanism of hyperdiploidy and how this phenomenon can potentially influence the expression profile of the genes is still unknown (22). The influence of hyperdiploidy in the course of CML remains a disputable question in literature. From clinical point of view, the chromosomal gain is associated with increased risk for blast crisis (23,24). To our knowledge, there is only one more report which presents higher percentage level of BCR-ABL transcript detected quantitatively and expressed in % (IS) (25). The detected level of the BCR-ABL transcript was measured to be 187% (IS) in bone marrow and 152% (IS) in peripheral blood of a 28-year-old patient.

As a whole the cytogenetic complexities play major role in the prognostic evaluation of CML. Along with the Ph chromosome, various chromosomal aberrations can be associated with CML. 5–10% of these cases showing complex translocation involving another chromosome in addition to the Ph chromosome. Our case is Ph(+) with an additional hyperdiploid clone with trisomy 8, 10, 12. Cases like this could sometimes present with higher results of BCR-ABL/ABL transcripts detected quantitatively.