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Introduction/background: Platelet membrane glycoproteins (GPs) serve several functions, the most significant of which is their role in primary hemostasis. Among these, GP IIb/IIIa is the primary fibrinogen receptor and is essential for platelet aggregation. Its deficiency or dysfunction impairs platelet aggregation, leading to Glanzmann thrombasthenia, a rare autosomal recessive bleeding disorder. In contrast, platelet GP IV (CD36) has a limited role in primary hemostasis. While also rare, CD36 deficiency has a disproportionately higher prevalence in individuals of East Asian, African, and Arabian descent. Patients with platelet GP deficiencies can develop antibodies against the missing GPs, leading to immune-mediated platelet transfusion refractoriness (PTR). Consequently, they are unresponsive to platelet transfusions when mostly needed.
Case Presentation: Here we present the case of an Egyptian male with a lifelong history of an incompletely characterized bleeding disorder who presented for pre-surgical evaluation. We diagnosed the patient with Type I Glanzmann thrombasthenia. Further evaluation revealed anti-CD36 antibodies, leading to the discovery of a concurrent platelet CD36 deficiency. The dual GP deficiency significantly complicated his management, as finding crossmatch-compatible platelets was challenging due to the rarity of CD36-deficient blood donors in the United States.
Discussion/conclusion: Awareness of coexisting platelet disorders and their ramifications is limited, mostly because these are stochastically rare (~1 in 100 million for the present case). This case highlights the importance of thoroughly evaluating platelet glycoprotein deficiencies, particularly in individuals with severe bleeding disorders and from ethnic backgrounds with a predisposition to specific platelet disorders. Such an approach can prevent future platelet antibody formation or reduce bleeding risk with pre-existing antibodies.
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http://dx.doi.org/10.1111/trf.18176 | DOI Listing |
Zhong Nan Da Xue Xue Bao Yi Xue Ban
May 2025
Department of Cardiovascular Medicine, Affiliated Changsha Hospital of Xiangya School of Medicine, Central South University, Changsha 410005.
Objectives: The Charlson comorbidity index reflects overall comorbidity burden and has been applied in cardiovascular medicine. However, its role in predicting in-hospital mortality in patients with acute myocardial infarction (AMI) complicated by ventricular arrhythmias (VA) remains unclear. This study aims to evaluate the predictive value of the Charlson comorbidity index in this setting and to construct a nomogram model for early risk identification and individualized management to improve outcomes.
View Article and Find Full Text PDFAnal Methods
September 2025
Department of Pharmaceutical Chemistry, College of Pharmacy, King Saud University, P.O. Box 2457, Riyadh 11451, Saudi Arabia.
Avapritinib (Ayvakit™) is a highly selective inhibitor of the platelet-derived growth factor receptor alpha (PDGFRA), including D842V mutations. Avapritinib (APB) is authorized in the United States for individuals with metastatic or unresectable gastrointestinal stromal tumors (GISTs). APB is considered the exclusive therapy for adults with indolent systemic mastocytosis.
View Article and Find Full Text PDFInt J Environ Health Res
September 2025
Department of Research, Unidad Médica de Alta Especialidad, Hospital de Especialidades, Instituto Mexicano del Seguro Social (IMSS), Veracruz, Mexico.
Little is known about the biomarkers of mortality in SARS-CoV-2-infected patients without a previous diagnosis of diabetes. Thus, this study aimed to assess the fibrinogen-to-platelet ratio (FPR) and compare its predictive value with the main biomarkers for COVID-19 mortality, such as neutrophil-to-lymphocyte ratio (NLR), platelet-to-lymphocyte ratio (PLR), leukocyte glucose index (LGI), and lactate dehydrogenase (LDH)/lymphocyte ratio. This retrospective cohort study in a population of Mexico included 70 non-diabetic patients with COVID-19 from 1 May 2020 to 30 September 2020.
View Article and Find Full Text PDFNurs Stand
September 2025
Herefordshire and Worcestershire Health and Care Trust, Worcester, England.
Bleeding disorders are rare congenital conditions where a person's blood does not clot correctly. The most common of these disorders is von Willebrand disease and the most well-known is haemophilia. However, less is known about rare bleeding disorders (RBDs), which collectively comprise a significant proportion of all bleeding disorders.
View Article and Find Full Text PDFBiomaterials
September 2025
Institute of Breast Health Medicine, State Key Laboratory of Biotherapy, West China Hospital, Sichuan University and Collaborative Innovation Center, Chengdu, Sichuan, 610041, PR China. Electronic address:
Host immune elimination largely limits the application of oncolytic viruses in clinics. Here, we rationally design a bioactive platelet-based oncolytic adenovirus delivery system. Upon loading adenoviruses, platelets are transformed to a pro-endocytosis status, which facilitates their internalization by circulating tumor cells (CTCs).
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