Platelet Storage Pool Deficiency of [Alpha] and [Delta] Granules.
[Alpha] granules contain a number of different proteins, including fibrinogen, platelet-derived growth factor, von Willebrand factor, factor V, fibronectin, [Beta]-thromboglobulin, and heparin-neutralizing factor (platelet factor 4).[1,2] [Delta] Granules contain calcium, serotonin, pyrophosphate, adenosine diphosphate, and adenosine triphosphate.[1,2] Determination of storage pool organelles by transmission electron microscopy allows the identification of storage pool defects. On electron microscopy, [Delta] granules are electron opaque owing to their high calcium content.
Platelet storage pool deficiencies comprise a range of disorders with variable degrees of reduction in the numbers and contents of [Alpha] granules, [Delta] granules, or both types of granules.[1,3] The term [Delta]-SPD has been used to identify patients who show only a diminished number of [Delta] granules. Patients with normal numbers of [Delta] granules but decreased [Alpha] granules are designated [Alpha]-SPD. Patients with both [Alpha]- and [Delta]-granule defects are designated [Alpha][Delta]-SPD. Patients with [Alpha]-SPD were originally described as having a "gray platelet syndrome" because of the agranular appearance of their platelets on peripheral blood smears. However, platelets from patients with [Alpha][Delta]-SPD also appear "gray" on blood smear owing to [Alpha]-granule deficiency. Electron microscopic studies have shown that the large vacuoles commonly filling the cytoplasm of [Alpha]-SPD platelets are virtually absent from platelets with the combined [Alpha][Delta] defect.
In most patients with platelet SPD, the platelets aggregate initially to adenosine diphosphate or epinephrine, but second-phase aggregation is frequently markedly diminished. Collagen-induced aggregation is also decreased.
In many patients the storage pool defect is the only abnormality detected. However, the defect has also been observed in patients with other congenital abnormalities, including Hermansky-Pudlak syndrome, Chediak-Higashi syndrome, Wiskott-Aldrich syndrome, and the syndrome of thrombocytopenia with absent radius.[1-3]
[1.] Weiss HJ, Witte LD, Kaplan KL, et al. Heterogeneity in storage pool deficiency: studies on granule-bound substances in 18 patients including variants deficient in [Alpha]-granules, platelet factor 4, [Beta]-thromboglobulin, and platelet-derived growth factor. Blood. 1979;54:1296-1319.
[2.] White JG. Inherited abnormalities of the platelet membrane and secretory granules. Hum Pathol. 1987;18:123-139.
[3.] Weiss HJ, Lages 13, Vicic W, et al. Heterogenous abnormalities of platelet dense granule ultrastructure in 20 patients with congenital storage pool deficiency. Br J Haematol. 1992;83:282-295.
Accepted for publication February 1, 2001.
From the Department of Pathology, University of Texas Health Science Center at Houston, Houston, Tex.
Reprints: David A. Biddle, MD, Department of Pathology, University of Texas Health Science Center at Houston, 6431 Fannin, MSB 2.292, Houston, TX 77030 (e-mail: David.A.Biddle@uth.tmc.edu).
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|Author:||Biddle, David A.; Neto, Tony G.; Nguyen, Andy N. D.|
|Publication:||Archives of Pathology & Laboratory Medicine|
|Date:||Aug 1, 2001|
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