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The Chromosomes in Polycythaemia Vera
Author(s) -
Kay H. E. M.,
Lawler Sylvia D.,
Millard Rosemary E.
Publication year - 1966
Publication title -
british journal of haematology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.907
H-Index - 186
eISSN - 1365-2141
pISSN - 0007-1048
DOI - 10.1111/j.1365-2141.1966.tb00134.x
Subject(s) - polycythaemia , bone marrow , medicine , clone (java method) , polycythemia vera , gastroenterology , pathology , immunology , biology , genetics , dna
T here have been few previous cytogenetic studies of patients with polycythaemia vera (P.V.). Nowell and Hungerford (1962) and Nowell (1965) investigated the chromosomes of the bone marrow and peripheral blood in five patients with polycythaemia who had been treated with radio‐phosphorus ( 32 P). They found abnormal cell lines in four patients, one of whom had developed leukaemia. Kemp, Stafford and Tanner (1961) examining the bone marrow by the short‐term culture method, found that seven out of nine cases of polycythaemia were normal, one patient had a cell line of 48 chromosomes, and one patient (who subsequently developed frank chronic granulocytic leukaemia) showed Ph 1 ‐positive cells. Both these patients had been treated with 32 P. An abnormal clone having a deletion of one of the C group chromosomes was present in the bone marrow of a patient with P.V. (Solari, Sverdlick and Viola, 1962): this patient had received X‐rays and 32 P. Levan, Nichols, Hall, Löw, Nilsson and Nordén (1964), using the blood leucocyte culture method, found hyperdiploid cell lines in a male patient with P.V. who had received 32 P. He had a few features of chronic granulocytic leukaemia. In all these previous studies, it is not known to what extent the chromosomal abnormalities are due to the disease or are secondary to treatment. It is clearly established that 32 P produces typical radiation damage of the chromosomes of blood leucocytes (MacDiarmid, 1965). A few cases of P.V. have been investigated in the terminal stages of the disease, after the development of a leukaemic state (Ford, Jacobs and Lajtha, 1958: one case; Baikie, Jacobs, McBride and Tough, 1961: two cases). In each case, short‐term bone‐marrow culture showed hypodiploid counts. The primary aim of the present study has been to give a general description of the chromosomal abnormalities in the bone marrow cells of 43 cases of P.V. Secondly we have attempted to relate these abnormalities to the stage and duration of the disease, including the development of leukaemia and bone‐marrow failure, and to the dose schedule and total amount of 32 P received. A search was made for phenotypic alterations in certain of the genetically defined characters of the blood cells. We have also made some comparisons between the chromosomal changes attributable to radiation in the bone‐marrow cells and the blood lymphocytes.