scholarly journals Platelet Function, Ultrastructure and Management in Glanzmann’s Thrombasthenia

1977 ◽  
Author(s):  
J.M. Lusher ◽  
M.I. Barnhart ◽  
J. Pullen ◽  
A.I. Warrier

This exhibit will demonstrate laboratory abnormalities found in longitudinal studies on six patients with Glanzmann’s thrombasthenia. All have had mucous membrane bleeding (predominantly epistaxis) since infancy. In addition to prolonged bleeding times, absent clot retraction and little or no platelet retention in a glass bead column, all six have defective platelet factor 3 release with Kaolin and their platelets do not aggregate with ADP, epinephrine or collagen. The platelets of all six do aggregate with ristocetin, however. Transmission electron microscopy (TEM) of thin sectioned platelets revealed normal ultrastructure. However, in the TEM platelet function test (Thromb. Diath. Haemorrh., Suppl. 42:321-344, 1970) there was difficulty in capturing the thrombasthenic platelets even on the formvar surface. Those platelets which did adhere to the formvar exhibited normal percentages of dendritic and spread forms although pseudopod detail was unusual. Inspection by scanning electron microscopy (SEM) of surfaces of platelets responding to contact activation and captured on companion formvar coverslips revealed surface membrane features consistent with inhibition of membrane activation. Platelets were swollen with convoluted membranes while pseudopod outgrowth from discrete regions was not prominent. Suppression of membrane activation was also noted by SEM of platelets obtained by cytocentrifugation of buffy coat preparations. Upon exposure to collagen platelet adhesion and morphologic features of aggregation were abnormal under our test conditions.In addition to local measures, recommended management of severe bleeding episodes is infusion of single donor platelet concentrates, obtained from an HLA matched donor by plateletpheresis.

1987 ◽  
Author(s):  
R M Hardisty ◽  
A Pannocchia ◽  
N Mahmood ◽  
T J C Nokes ◽  
D Pidard ◽  
...  

A 17-year-old Italian boy has had a lifelong bleeding tendency, with frequent epistaxes and gum bleeding. The bleeding time is prolonged and the platelet count low normal. Electron microscopy showed a wide diversity of platelet size with many giant forms. In citrated PRP, ADP and other agonists induce slow and incomplete aggregation. The response of washed platelets varied with the agonist but ranged from subnormal to almost normal. Fibrinogen binding to washed platelets occurred slowly in response to ADP but eventually approached normal levels. No significant abnormality was observed of 5HT uptake, adenine nucleotide content, platelet factor-3 availability, β-thromboglobulin content or release, or malonyldialdehyde production. Clot retraction was normal. SDS-PAGE showed reduced amounts of GPIIb and GPU Ia. Crossed immunoelectrophoresis of Triton X-100 extracts of washed platelets showed the presence of GPIIb/IIIa complexes at 25-50% of normal levels. SDS-PAGE combined with an immunoblot procedure confirmed unchanged mobilities of GPIIb and GPIIIa and a normal proportion of GPIIb to GPIIIa. However, binding studies with radiolabelled monoclonal antibodies showed that intact washed platelets expressed only 12-20% of the normal binding sites for M148, AP-2 and Tab. These antibodies recognize different epitopes on GPIIb/lIIa complexes. Similar levels of these glycoproteins were detected by autoradiography after SDS-PAGE of radio-iodinated patient's platelets. GP lb was normally present. A possible defect in the exposure of fibrinogen binding sites might contribute to the altered platelet function. Meanwhile, the patient appears to be a unique variant of Glanzmann's thrombasthenia with GP IIb/IIIa complexes at the borderline of those able to support platelet aggregation.


1983 ◽  
Vol 49 (03) ◽  
pp. 182-186
Author(s):  
G T E Zonneveld ◽  
E F van Leeuwen ◽  
A Sturk ◽  
J W ten Cate

SummaryQuantitative glycoprotein (GP) analysis of whole platelets or platelet membranes was performed by SDS-polyacrylamide gelelectrophoresis (SDS-PAGE) and periodic acid Schiff staining in the families of two unrelated Glanzmann’s thrombasthenia (GT) patients. Each family consisted of two symptom free parents, a symptom free daughter and a GT daughter. All symptom free members had a normal bleeding time, clot retraction and platelet aggregation response to adenosine 5’-diphosphate (ADP), collagen and adrenalin. Platelet Zw* antigen was normally expressed in these subjects. GT patiens, classified as a type I and II subject, showed reduced amounts of GP lib and of GP nia. Analysis of isolated membranes in the non-reduced state, however, showed that the amount of GP Ilia was also reduced in three of the four parents, whereas one parent (of the GT type I patient) and the two unaffected daughters had normal amounts of GP Ilia. Quantitative SDS-PAGE may therefore provide a method for the detection of asymptomatic carriers in GT type I and II.


2018 ◽  
Vol 2 (02) ◽  
pp. 59-60
Author(s):  
Farida Yasmin ◽  
Md. Anwarul Karim ◽  
Chowdhury Yakub Jamal ◽  
Mamtaz Begum ◽  
Ferdousi Begum

Epistaxis in children is one of the important presenting symptoms for attending emergency department in paediatric patients. Recurrent epistaxis is common in children. Although epistaxis in children usually occurred due to different benign conditions, it may be one of the important presenting symptoms of some inherited bleeding disorder. Whereas most bleeding disorders can be diagnosed through different standard hematologic assessments, diagnosing rare platelet function disorders may be challenging. In this article we describe one case report of platelet function disorders on Glanzmann’s thrombasthenia (GT). Our patient was a 10-year old girl who presented to us with history of recurrent severe epistaxis. She had a bruise on her abdomen and many scattered petechiae in different parts of the body. Her previous investigations revealed no demonstrable haemostatic anomalies. After performing platelet aggregation test, she was diagnosed as GT.


1979 ◽  
Author(s):  
E.F. von Leeuwen ◽  
G.T.E. Zonneveld ◽  
L.E. von Riesz ◽  
C.S.P Jenkins ◽  
J.A. van Mourik ◽  
...  

The expression of the platelet-speciftc alloantigens on the platelets from 6 patients with Glanzmann’s Thrombasthenia (G.T.) and their nearest relatives was studied. The alloantigens Zwa (PIAl) and Zwb(PIA2) were found to be completely absent from thrombasthenic platelets while the alloantigens of the Ko-system were found to be normally expressed. The alloantigen Baka(phenotypefrequency 90.2%) was absent on the platelets from 4 studied G.T. patients. The platelets of all the family members reacted positively with anti-Zwa, negatively with antt-Zwb serum. SDS-PA gel electrophoresis of G.T. platelet membranes demonstrated a marked deficiency of the glycoproteins IIb and IIIa. Glycoprotein analysis of the platelet membranes from the family members of 3 of the 6 patients reveoled no apparent abnormalities.Pre-incubation with anti-Zwa containing plasma strongly inhibits ADP-and collagen induced aggregation of platelets from normal Zwa homozygous individuols with a slight inhibition of the aggregation induced by ristocetin. Zwa antibodies did not affect the functions of platelets from ZWb homozygous individuals. Thus binding of Zwa antibodies induces a thrombosthenis-like state.


Blood ◽  
1971 ◽  
Vol 37 (2) ◽  
pp. 163-171 ◽  
Author(s):  
CHRISTINE A. JOHNSON ◽  
CHARLES F. ABILDGAARD ◽  
IRVING SCHULMAN

Abstract Results of a comparative study of the functional capacity of young versus old platelets are presented. A girl with thrombopoietin deficiency, who predictably produced platelets in response to plasma transfusion, was used as platelet donor. Her platelets obtained 4 days after infusion were used as young test cells. Platelets obtained at 18 or 21 days after infusion were used as old cells. Young platelets were found to be associated with normal bleeding times, normal clot retraction, normal or increased platelet adhesiveness, normal aggregation to ADP and collagen, and normal platelet factor 3 availability. Old platelets were found to be associated with long bleeding times, decreased platelet adhesiveness in vivo and in vitro, and deficient platelet factor 3 availability. The clot retraction and aggregation to ADP and collagen of old platelets, however, was normal. No differences between young and old platelets were observed by electron microscopy.


1999 ◽  
Vol 56 (9) ◽  
pp. 495-498
Author(s):  
Alberio ◽  
Hirt

Der Fall eines Patienten mit einer seit Geburt vorhandenen mukokutanen Blutungsneigung wird vorgestellt. Es wurde eine Thrombasthenie Glanzmann diagnostiziert. An diesem Beispiel werden wichtige Aspekte der Diagnostik und Therapie von Thrombozytenfunktionsstörungen beschrieben. Zudem wer-den die Thrombozytenbeteiligung im Blutstillungsvorgang sowie die Rolle des thrombozytären Fibrinogen-Rezeptors Glykoprotein IIb–IIIa im Rahmen der primären Hämostase dargestellt.


Blood ◽  
2012 ◽  
Vol 120 (21) ◽  
pp. 3341-3341
Author(s):  
Rainer Zotz ◽  
Giovanni di Minno ◽  
Roseline d'Oiron ◽  
Man-Chiu Poon

Abstract Abstract 3341 Background. Glanzmann's thrombasthenia (GT) is a severe inherited bleeding disorder with defective platelet membrane αIIbβ3. Until now there have been only limited data regarding treatment of GT with platelets (P), NovoSeven (rFVIIa), and antifibrinolytics (AF) in children. Methods. The GTR is an international prospective multicenter registry on the efficacy and safety of rFVIIa as well as platelets and AF for non-surgical and surgical bleedings in GT patients. From 2004 to 2011, 218 GT patients from 45 sites in 15 countries from 4 continents were enrolled in the GTR, including 106 children. In the following the terms “rFVIIa”, “P”, and “rFVIIa+P” may include use of AF. “AF” means AF only. Results for surgical bleedings. Of the 96 patients with surgical procedures (n=204), 27 (28%) were children (21 < 12 yrs, 6 adolescents 12–17 yrs) with 42 procedures (21%). Dental procedures were the most frequent intervention (n=26, 62%), followed by nasal procedures (n=4, 10%), and gastrointestinal surgery and excision (each n=3, 7%). The majority of surgeries were treated equally often with rFVIIa (n= 14, 33%) and P (n=12, 29%), followed by rFVIIa+P (n=9, 21%) and AF (n=7, 17%). In major surgical procedures (n=8, 19%), children were mostly treated with rFVIIa (n=3, 38%) or with rFVIIa+P (n=3, 38%), while P (n=1, 13%) or AF (n=1, 13%) was used less often. In minor procedures (n=34), P or rFVIIa were administered about twice as often as rFVIIa+P, or AF, respectively (P: n=11, 26%, rFVIIa: n=11, rFVIIa+P: n=6, 14%, AF: n=6). rFVIIa (7/26, 27%), P (8/26, 31%) and AF (7/26, 27%) were used equally often in dental procedures (rFVIIa+P 4/26, 15%). When children were treated with AF in surgery, it was always in dental procedures (7/7). The median dose was 93μg/kg. Regarding the efficacy of the different treatments, rFVIIa was 100% successful (14/14), as well as P (12/12). The efficacy of rFVIIa+P was 56% (5/9), that of AF 43% (3/7). There were no rebleedings. The numbers of minor and major procedures stratified according to the presence of antibodies and/or refractoriness are too low to allow for a separate analysis. Results for non-surgical bleedings. Out of 184 GT patients with non-surgical bleeding, 105 were < 18 years old. No history of antibodies (AB) and/or refractoriness (REF) was present in 86 of these patients (82%). AB were documented in 11 (10.5%); REF in 3 (2.9%); and REF + AB in 5 (4.8%). Bleeding (n=628) was moderate in 483 (77%) and severe in 145 (23%) episodes. Among moderate bleedings, 286/483 (59%) were spontaneous; among severe bleedings, 130/145 (90%) were spontaneous. In moderate bleedings, rFVIIa was used in 175 (36%) episodes; P in 153 (32%); AF in 130 (27%); and rFVIIa+P in 25 (5.2%). In severe bleedings, rFVIIa was used in 22 (15%) episodes; P in 62 (43%); rFVIIa+P in 22 (15%); and AF in 39 (27%). The median dose of rFVIIa was 90μg/kg. The proportion of successful treatments (bleeding stopped within 6 h of starting treatment) for rFVIIa was 78% for spontaneous and 87% for traumatic bleeding. These figures were 74% and 79%, respectively, with P; 71% and 43%, respectively, with rFVIIa+P; and 82% and 89%, respectively, with AF only. The numbers were too low to allow for a stratification for presence of AB and/or REF. Treatment failure was documented in only 13 episodes (2% of 628), 8 having received only AF. Out of 628 bleedings, 37 re-bleedings (bleedings re-starting within 6–24 h after having stopped) were registered: 6/197 after treatment with rFVIIa (3%), 20/215 with P (9.3%), 8/47 with rFVIIa+P (17%) and 3/169 with AF (1.8%). Thromboembolic events were not reported. Allergic reactions were reported following treatment with P (3/215, 1.4%). Conclusions. The GTR results for children show that the efficacy of rFVIIa was as good as that of P. rFVIIa was safe. In non-surgical bleedings, P were preferred in all cases but traumatic moderate bleeding (preference for rFVIIa); surgical bleedings were treated equally often with rFVIIa and P. Overall, the efficacy was high for all treatment options. The re-bleeding rate was higher after P only than after rFVIIa only in non-surgical bleedings. The merit of the combined use of rFVIIa and platelets could not be assessed in this non-randomized study since the combined treatment is usually applicated in cases of severe bleeding with insufficient success of single treatment options. Disclosures: Zotz: Novo Nordisk: Honoraria. Off Label Use: Recombinant actived FVII. di Minno:Novo Nordisk: Honoraria. d'Oiron:NovoNordisk: Honoraria. Poon:Novo Nordisk: Honoraria.


1996 ◽  
Vol 33 (5) ◽  
pp. 503-511 ◽  
Author(s):  
M. K. Boudreaux ◽  
K. Kvam ◽  
A. R. Dillon ◽  
C. Bourne ◽  
M. Scott ◽  
...  

An 8-month-old female Great Pyrenees dog with chronic epistaxis and a history of gingival bleeding during shedding of deciduous teeth was evaluated for platelet function. Platelet morphology was normal at both the light and electron microscopic level. Platelet number and mean platelet volume were also normal. Platelet aggregation responses to adenosine diphosphate, collagen, platelet activating factor, and thrombin were markedly reduced, although shape change responses were normal. Clot retraction was markedly impaired. Monoclonal antibody (MoAb) Y2/51, a murine anti-human platelet β3 antibody that cross-reacts with canine platelet β3 , and MoAb 5G11, a murine anti-dog platelet αIIbβ3 antibody, bound minimally to affected dog platelets, as demonstrated by flow cytometry. Binding of MoAb Y2/51 was not detectable by immunoblot. MoAb CAP1, a murine anti-dog fibrinogen receptor-induced binding site antibody, failed to bind to affected dog platelets, as demonstrated by flow cytometry. A reduction in glycoproteins αIIb and β3 was demonstrated by two-dimensional protein electrophoresis. This is the first reported case of type I Glanzmann's thrombasthenia in the dog that closely resembles the clinical syndrome and the platelet morphology described in type I Glanzmann's thrombasthenia of human beings.


1972 ◽  
Vol 48 (2) ◽  
pp. 116-124 ◽  
Author(s):  
A.K. Saraya ◽  
Jaya Kasturi ◽  
Ram Kishan

Sign in / Sign up

Export Citation Format

Share Document