Die megakaryozytäre Myelose — Klinik, Morphologie und Plättchenfunktion
- 1 January 1989
- journal article
- research article
- Published by Springer Nature in Journal of Molecular Medicine
- Vol. 67 (2) , 51-59
- https://doi.org/10.1007/bf01735652
Abstract
The study reviews 22 patients, aged between 19 to 73 years, with megakaryocytic myelosis. In the course of the disease 11 patients presented haemorrhagic manifestations, 12 patients thrombotic complications, and 6 patients the association of haemorrhage and thrombosis. The maximum platelet counts ranged from 524 to 2700×109/l. The bone marrow showed a conspicuous megakaryocytic proliferation with polyploidy of the nuclei, giant forms and clusters. Marked alterations of erythro- and granulopoiesis were excluded. There was no evidence for a reactive thrombocytosis in any case. Patients with thrombocythaemia due to megakaryocytic myelosis (n=14), with secondary thrombocytosis of various origin (n=16), and a control group of healthy donors (n=20) were investigated with respect to the aggregation behaviour and the total calcium content of blood platelets. In 9 of 14 patients with megakaryocytic myelosis platelet rich plasma did not respond to epinephrine (15 µmol/l), a concentration which induced at least weak aggregation in 14 of 16 patients with secondary thrombocytosis and also in healthy subjects. In patients with megakaryocytic myelosis the mean extent of aggregation induced by epinephrine, collagen or adenosine diphosphate was significant lower as compared to controls whereas in patients with secondary thrombocytosis in most cases this parameter did not differ significantly from that of controls. The total calcium content of platelets was significantly lower in both groups of patients as compared to controls. In 14 patients with megakaryocytic myelosis the concentration of the glycoprotein (GP) IIb-IIIa complex was estimated by crossed- and rocket-immunoelectrophoresis and found to be decreased in 8 of them. The amount of GP IIb-IIIa correlated inversely with the platelet count (r=−0,66). The results may contribute to better pathophysiological understanding of the megakaryocytic myelosis, thrombocythaemias in myeloproliferative disorders and their complications.Keywords
This publication has 46 references indexed in Scilit:
- Acute leukemia following treatment of polycythemia vera and essential thrombocythemia with uracil mustardAmerican Journal of Hematology, 1988
- Platelet function in myeloproliferative disorders: Characterization and sequential studies show multiple platelet abnormalities, and change with timeEuropean Journal of Haematology, 1988
- Essential thrombocythemias. Clinical evolutionary and biological dataCancer, 1986
- PLATELET MEMBRANE GLYCOPROTEIN ABNORMALITIES IN MYELOPROLIFERATIVE DISEASEBritish Journal of Haematology, 1986
- Working classification of chronic myeloproliferative disorders based on histological, haematological, and clinical findings.Journal of Clinical Pathology, 1986
- Dissociation of the glycoprotein IIb-IIIa complex in isolated human platelet membranesBiochimica et Biophysica Acta (BBA) - Biomembranes, 1982
- Protein and Glycoprotein Abnormalities in an Unusual Subtype of Glanzmann’s ThrombastheniaPathophysiology of Haemostasis and Thrombosis, 1982
- Platelets in Myeloproliferative Disorders. III: Glycoprotein Profile in Relation to Platelet Function and Platelet DensityScandinavian Journal of Haematology, 1981
- Platelet Function in Essential ThrombocythemiaNew England Journal of Medicine, 1978
- General Remarks on Principles, Equipment, Reagents and ProceduresScandinavian Journal of Immunology, 1973