| 摘要 |
A method for differential diagnostics of true polycythemia and secondary erytrocytosis comprises screening of peripheral blood for the presence of mutation V617F of the gene JAK2 by polymerase chain reaction. The presence of splenomegaly, dermal itch after “hydrotherapeutic procedures”, parameters of general blood test – number of erythrocytes, leucocytes, blood plates, neutrophils, the level of lactate dehydrogenase and serum erythropoietin, the presence of three-germ marrow hyperplasia according to trepanobiopsy data are determined with subsequent determination of probability of disease presence. |
