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2020, Number 3

Rev Hematol Mex 2020; 21 (3)

The clinical application of Della-Porta et al score in a Mexican patient with myelodysplastic syndrome

Marín-Corte JC, Olmedo-Gutiérrez E, Marín-Corte JA, Miranda RN, Bueso-Ramos CE, Cano-Jiménez O, Fuentes-Reyes AR, Hernández-Salamanca E, López-Trujillo MA, Marín-López RA, Ruiz-Delgado GJ, Ruiz-Argüelles GJ
Full text How to cite this article

Language: English
References: 12
Page: 158-171
PDF size: 497.55 Kb.


Key words:

Myelodysplastic syndrome, Bone marrow.

ABSTRACT

Background: The myelodysplastic syndromes are one of the most studied diseases in hematology in recent years. By definition and according to the World Health Organization Classification of Tumours of hematopoietic and Lymphoid Tissues 2017, myelodysplastic syndromes are a group of clonal hematopoietic stem cell diseases characterized by cytopenia, dysplasia in one or more of the major myeloid lineages, ineffective hematopoiesis, recurrent genetic abnormalities and increased risk of developing acute myeloid leukemia (AML). To identify in a quick way this disease, we designed a worksheet based on the article of Matteo Della-Porta et al to developed a systematic approach to assess the morphological features in the bone marrow smears of three cell lineages in patients with myelodysplastic syndromes and provide the basis to validate flow cytometric and immunohistochemistry data.
Clinical case: A 47-year-old male patient in whom we applied a worksheet that we designed based on Della-Porta score criteria to each cellularity lineage in the bone marrow smears and we obtained significant results according to the bone marrow biopsy final report.
Conclusions: If we apply the worksheet that we designed base on Della-Porta score in the bone marrow smears myelograms, we can identify in early stages myelodysplastic syndromes processes.


REFERENCES

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Rev Hematol Mex. 2020;21