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      A Morphometric Analysis of Platelet Dense Granules of Patients with Unexplained Bleeding: A New Entity of Delta-Microgranular Storage Pool Deficiency

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          Abstract

          One thousand and eighty patients, having prolonged bleeding times, frequent epistaxis, menorrhagia or easy bruising or other bleeding manifestations, and excluding those with von Willebrand’s disease, were evaluated for platelet dense granule deficiency. The mean diameter of platelet dense granules was determined for all patients using image analysis. Four hundred and ninety-nine had “classic” dense (delta) granule storage pool deficiency (δ-SPD). Five hundred and eighty-one individuals (53.8%) were found to have a normal mean number of dense granules, but for some of these patients, the dense granules were smaller than for the controls. Of the patients having a normal number of dense granules, 165 (28.4%) were found to have significantly smaller granules than the platelets obtained from the control subjects. Their average granule diameter was 123.35 ± 0.86 nm, that is more than three standard deviations below the mean of the control data. Total δ-granule storage pool volumes (TDGV)/platelet were calculated using these measurements. Individuals with δ-SPD had half the number of granules (2.25 ± 0.04 DG/PL) and storage pool volume (3.88 ± 1.06 × 10 6 nm 3) when compared to our control data (4.64 ± 0.11 DG/PL; 10.79 × 10 6 nm 3 ± 0.42). Individuals having a bleeding history but a normal average of small dense granules had a calculated storage pool volume statistically different than controls and essentially the same storage pool volume as patients with δ-SPD. We have identified a sub-classification of δ-SPD that we have defined as micro-granular storage pool deficiency (δ-MGSPD).

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          A low-viscosity epoxy resin embedding medium for electron microscopy.

          A R Spurr (1969)
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            The platelet release reaction: granules' constituents, secretion and functions.

            Although anucleated, blood platelets are highly organized cells rich in different types of organelles. Three specific granule populations store different types of constituents, some of which are at high concentrations. Platelets thus transport some specific compounds through the whole body. During circulation, platelets are reactive to various stimuli and release the materials stored in the specific granules. This 'release reaction' is an important step of primary haemostasis. Energy and messengers required for platelet reactivity are provided by mitochondria and the dense tubular system. Each granule population has specific properties concerning both the structure and the role played by the released constituents. Dense granules contain small non-protein molecules that are secreted to recruit other platelets. alpha-Granules contain large adhesive and healing proteins. Lysosomes contain hydrolases able to eliminate the circulating platelet aggregate. The extrusion of storage granules' content to the platelet's environment occurs according to regulated secretion events: movements of granules, apposition and fusion of granule and plasma membranes. Typical platelet disorders resulting from a storage granule abnormality are referred to as a storage pool defect and are characterized by a prolonged bleeding time.
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              Reliability of absent platelet dense bodies as a diagnostic criterion for Hermansky-Pudlak syndrome.

              The clinical, pigmentary, and ceroid storage manifestations of the Hermansky-Pudlak syndrome (HPS) triad of albinism, hemorrhagic diathesis, and ceroid storage disease are variable. Therefore, a rapid and accurate method of diagnosing HPS is needed. Platelets of 66 albinos were examined by electron microscopy for the presence or absence of dense bodies. Results show that patients reexamined over a period of 1 year had consistent findings. Those lacking dense bodies (15) when first examined also lacked dense bodies when reexamined a year later, and they had evidence of ceroid storage. Those with dense bodies when first examined (8) also had dense bodies when reexamined, did not have evidence of storage disease, and had types of albinism other than HPS. Of 20 propositi lacking dense bodies, all 32 albino relatives also lacked dense bodies, while 6 albino relatives of 6 propositi with dense bodies also had dense bodies in their platelets. The evidence supports the concept that HPS is a distinct genetic and biochemical disease in which the components of the triad are the result of a single genetic defect, either a point mutation or a small deletion. Comparison of whole mount preparations with thin section preparations of 13 albinos shows that whole mount preparations are an accurate and rapid method for diagnosing HPS. The most consistent diagnostic feature of HPS is lack of platelet dense bodies.
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                Author and article information

                Journal
                J Clin Med
                J Clin Med
                jcm
                Journal of Clinical Medicine
                MDPI
                2077-0383
                04 June 2020
                June 2020
                : 9
                : 6
                : 1734
                Affiliations
                [1 ]Department of Pathology, University of Ohio, Toledo, OH 43614, USA; edward.calomeni@ 123456osumc.edu
                [2 ]Kansas City University of Medicine and Biosciences, Kansas City, MO 64106, USA; mraghavan@ 123456kcumb.edu
                [3 ]New York State Department of Health, Albany, NY 12203, USA; jturner@ 123456binghamton.edu
                [4 ]Department of Electrical and Computer Engineering, University of Houston, Houston, TX 77204, USA; broysam@ 123456central.uh.edu
                [5 ]Independent Researcher, Houston, TX 77002, USA; shantala.roysam@ 123456gmail.com
                [6 ]Department of Medicine, University of Toledo, Toledo, OH 43614, USA; maryrsmith@ 123456utoledo.edu
                [7 ]Mary Gooley Hemophilia Center, Rochester General Hospital, Rochester, NY 14621, USA; peter.kouides@ 123456rochesterregional.org
                [8 ]Wilmot Cancer Institute, University of Rochester Medical Center, Rochester, NY 14642, USA; Neil_Lachant@ 123456URMC.Rochester.edu
                Author notes
                Author information
                https://orcid.org/0000-0002-4190-2479
                https://orcid.org/0000-0002-6664-0479
                https://orcid.org/0000-0003-4637-4211
                Article
                jcm-09-01734
                10.3390/jcm9061734
                7356033
                32512725
                95dde5a9-4057-4480-a6d2-0c8b37c5c2eb
                © 2020 by the authors.

                Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license ( http://creativecommons.org/licenses/by/4.0/).

                History
                : 05 March 2020
                : 01 June 2020
                Categories
                Article

                unexplained bleeding,platelet storage pool deficiency,platelet dense granules

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