Erythraemic Myelosis Terminating in Erythroleukaemia
نویسندگان
چکیده
منابع مشابه
Biochemical abnormalities in chronic erythraemic myelosis.
For a number of years, considerable interest and much investigation has been directed at a group of disordcrs characterized by refractory niacrocytic anaemia, monocytosis, leukopenia, nicgaloblastoid erythroid liyperplasia of the bone marrow, ineffective erythropoiesis with increased serum iron and decreased plasma iron turnover, and in some instances transformation into acute niyeloblastic or ...
متن کاملChronic lymphatic leukaemia terminating as erythroleukaemia.
Case report A 67-year-old man presented in May 1978 with malaise and splenomegaly. Initial blood count showed haemoglobin 12-1 g/dl, total white cell count 25 7 x 10'/1 (polymorphs 5 %, lymphocytes 93 %, eosinophils 2 %), platelet count 98 x 10'/1. Bone marrow examination showed a 66% infiltration by mature lymphocytes. Haematopoiesis otherwise was morphologically normal. A diagnosis of chronic...
متن کاملMyelosis involving the granulocytic and erythrocytic systems.
There are several syndromes in which an erythriblastic reaction, comparable with the granulocytic reaction of granulocytic leukaemia, is prominent. One is the "leukanaemia" of von Leube (1900) defined by Foy, Kondi, and Murray (1946) as " a haematological condition in which there co-exist a pernicious anaemia-like and a leukaemia-like blood picture with corresponding marrow disorder of the eryt...
متن کاملAcute erythremic myelosis (true erythroleukaemia): a variant of AML FAB-M6.
AIMS Classic erythroleukaemia (acute myeloid leukaemia M6, or M6 AML) is defined as an excess of myeloblasts in an erythroid predominant background. Leukaemia variants in which the primitive blast cells are demonstrably erythroid are extremely rare and poorly characterised. Variably referred to as "true erythroleukaemia" or "acute erythremic myelosis", they are often included within the M6 AML ...
متن کاملA case of systemic lupus erythematosus with sideroblastic anaemia terminating in erythroleukaemia.
A case of systemic lupus erythematosus is described in which for 10 years the only significant findings were erythema multiforme and vasculitis. Gross hepatosplenomegaly with persistent pancytopenia developed, and bone marrow examination revealed the presence of sideroblasts. The patient's condition deteriorated, and subsequently she developed a severe bleeding tendency, terminating in erythrol...
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ژورنال
عنوان ژورنال: BMJ
سال: 1955
ISSN: 0959-8138,1468-5833
DOI: 10.1136/bmj.1.4922.1124