Journal Logo



Savchuk, A.1; Cabrera, W.2; Sola, E.1; Cornago, J.3; Del Campo, J. F.4; López-Pereira, P.1; Orfao, A.5; Álvarez-Twose, I.6; Steegmann, J. L.1

doi: 10.1097/01.HS9.0000566336.28751.9f
Publication Only: Chronic myeloid leukemia - Clinical

1Hematology, Hospital La Princesa, Madrid, Spain

2Hematology, Hospital Materno Infantil, Caja Nacional de Salud, Universidad Mayor de San Andres, La Paz, Bolivia, Plurinational State Of

3Hematology, Hospital Fundación Jiménez Díaz

4Hematology, Hospital del Henares, Madrid

5Servicio General de Citometría (NUCLEUS), Departamento de Medicina, Centro de Investigación del Cáncer (IBMCC-CSIC/USAL and IBSAL, Universidad de Salamanca, Salamanca

6Instituto de Estudios de Mastocitosis de Castilla La Mancha (CLMast), Hospital Virgen del Valle, Toledo, Spain

Back to Top | Article Outline


We present here the case of a 52 year old male patient who was diagnosed of D816 V + indolent systemic mastocytosis in 2006. The patient received only symptomatic treatment with fexofenadine, sodium cromoglycate, and ranitidine. In November 7th 2016, mild leukocytosis was detected in one of the screenings. The patient had not symptoms or signs of CML or mastocytosis. WBC was 14.04 x 109/L, Hb: 15,5 g/dl; Platelet 832 x 109/L. Serum tryptase was normal (5.4 ng/ml). led to the diagnosis of Ph1+, BCR-ABL, e14a2 positive CML. Cytologic exam of the bone marrow (BM) disclosed a typical picture of chronic phase of CML and 0.2% mastocytes. Karyotyping disclosed typical t(9;22) in 95% of the BM metaphases. Mutational analysis. Mastocytes and CD34+ cells were sorted by FACSAria. The mutation D816 V (pAsp816/Val) was assessed by PNA-PCR and NGS, and was not detected either in CD34+ cells, or in mastocytes (this last result being not conclusive, because of the low number of mastocytes present in the BM (675 cells). Jak2V617F was not present.BCR-ABL detection. RT-PCR in BM disclosed e14a2 transcript. FISH analysis was performed in the sorted populations, and was detected in CD34+ (84%), Monocytes (61%), neutrophils (88%), eosinophils (73%), and mesenchymal cells (16%). It was negative in lymphocytes, and although 8 out of 18 mastocytes were positive, this percentage was inconclusive.

Back to Top | Article Outline


To describe an extremely rare case of Chronic myeloid leukemia developing after systemic mastocytosis.

Back to Top | Article Outline



Back to Top | Article Outline


Hydrea was used from January 10 th to April 21 st 2017, and Imatinib 400 QD was started four days later.Table 1 depicts the evolution of molecular response. The treatment obtained major molecular response, MR4, and MR5 in 3, 6 and 9 months respectively.MR5 was sustained at 18 months of imatinib treatment. Serum tryptase diminished, probably because of the effect of imatinib on wild-type c-Kit.AEs were all of grade 1, and included eye-lid edema, weight gain, and vomiting.



Back to Top | Article Outline


The case here described is the second case reported of CML arising in a patient with D816 V mastocytosis. In 2005, Agis et al reported one case of typical CML with concurrent systemic, D816 V mastocytosis. In that case Imatinib treatment resulted in complete cytogenetic response 1. In our case, in spite of the presence of mastocytes in BM, we did not detect either the D816 V mutation, or the BCR-ABL signal in the mastocytes. The absence of D816 V in CD34 cells support the notion that BCR-ABL translocation is independent to the previous existence of SM. This independence is also sustained by the extreme rarity of this association. From the clinical point of view, our case shows that Imatinib treatment could induce in a very fast deep molecular response, with mild adverse effects, in this extremely rare association.

Copyright © 2019 The Authors. Published by Wolters Kluwer Health Inc., on behalf of the European Hematology Association.