Thromb Haemost 1989; 62(03): 846-849
DOI: 10.1055/s-0038-1651015
Original Article
Schattauer GmbH Stuttgart

Arterial Thrombosis Associated with Immune Thrombocytopenia: Presence of a Platelet Aggregating IgG Synergistic with Thrombin and Adrenalin

Shaun P Jackson
The Department of Medicine, Monash Medical School, Commercial Road, Prahran, Victoria, Australia
,
Stephen M Jane
The Department of Medicine, Monash Medical School, Commercial Road, Prahran, Victoria, Australia
,
Christina A Mitchell
The Department of Medicine, Monash Medical School, Commercial Road, Prahran, Victoria, Australia
,
W Fernando Cortizo
The Department of Medicine, Monash Medical School, Commercial Road, Prahran, Victoria, Australia
,
Lena Hau
The Department of Medicine, Monash Medical School, Commercial Road, Prahran, Victoria, Australia
,
Sharron L Pfueller
The Department of Medicine, Monash Medical School, Commercial Road, Prahran, Victoria, Australia
,
Hatem H Salem
The Department of Medicine, Monash Medical School, Commercial Road, Prahran, Victoria, Australia
› Author Affiliations
Further Information

Publication History

Received 01 March 1988

Accepted after revision 28 July 1989

Publication Date:
30 June 2018 (online)

Summary

We report the case of a 50-year-old lady who presented with arterial thrombosis in the setting of thrombocytopenia. Investigations confirmed the diagnosis of idiopathic thrombocytopenic purpura. A spontaneous platelet aggregating factor (SPAF) was isolated from the immunoglobulin fraction of the patient's plasma. The isolated IgG irreversibly aggregated platelet-rich plasma and washed platelets, an effect abolished by pretreating the platelets with aspirin. The activity of the IgG was greatly enhanced by subaggregatory concentrations of thrombin and adrenalin and was localized to the F(ab')2 of the molecule. Plasmapheresis in combination with anti-platelet therapy resulted in an increase in the patient's platelet count, reduced platelet aggregating activity of plasma and significant clinical improvement.

We suggest that the presence of this platelet aggregating IgG contributed to the development of thrombosis in our patient and postulate that a similar factor may explain the paradox of thrombosis observed in a select group of thrombocytopenic patients.

 
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