Pseudothrombocytopenia: Manifestation of a New Type of Platelet Agglutinin

Author:

Shreiner David P.12,Bell William R.13

Affiliation:

1. Department of Medicine, The Johns Hopkins University School of Medicine and Hospital, Baltimore, Md. 21205; the Veterans Administration Hospital, Oakland Division, and the University of Pittsburgh Medical School, Pittsburgh, Pa. 15213.

2. Department of Medicine. University of Pittsburgh School of Medicine. Pittsburgh. Pa. 15213: Chief. Division of Nuclear Medicine. Veterans Administration Hospital. Oakland Division. Pittsburgh. Pa. 15240: formerly held a hematology fellowship at The Johns Hopkins University School of Medicine and Hospital. and was supported by a Graduate Training Grant. TI-AM-5260, from the National Institute of A

3. Department of Medicine. The Johns Hopkins University School of Medicine and Hospital. Baltimore. Md. 21205: Hubert E. and Anne E. Rogers Scholar in Academic Medicine.

Abstract

Abstract Spuriously low electronic platelet counts were obtained on blood collected in EDTA from six patients. Platelet numbers on blood smears and electronic counts performed on blood collected in other anticoagulants were normal. Plasma or sera from these patients agglutinated homologous, as well as autologous platelets, in the presence of EDTA or DTPA, but agglutination did not occur in blood or platelet-rich plasma anticoagulated with heparin, oxalate, or citrate. Agglutination in the presence of EDTA was not inhibited by heparin, α-tocopherol, or N-ethylmaleimide, but was inhibitied by excess EDTA or divalent cation. The agglutinin was temperature independent in five of the six patients and had the physical and immunologic characteristics of a gamma globulin. The clinical significance and mechanism of EDTA-dependent agglutination of platelets is unknown.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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