Sekayan Tro, Allen Elizabeth S, Kopko Patricia, Stephens Laura D, Zhao Mitchell, Curtis Brian R, Sullivan Mia J, Trapp-Stamborski Valerie, von Drygalski Annette
Department of Medicine, Division of Hematology/Oncology, University of California San Diego, San Diego, California, USA.
Department of Pathology, Division of Laboratory and Genomic Medicine, University of California San Diego, San Diego, California, USA.
Transfusion. 2025 Apr;65(4):767-772. doi: 10.1111/trf.18176. Epub 2025 Mar 3.
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.
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.
引言/背景:血小板膜糖蛋白(GPs)具有多种功能,其中最重要的是它们在初级止血中的作用。其中,GP IIb/IIIa是主要的纤维蛋白原受体,对血小板聚集至关重要。其缺乏或功能障碍会损害血小板聚集,导致Glanzmann血小板无力症,这是一种罕见的常染色体隐性出血性疾病。相比之下,血小板GP IV(CD36)在初级止血中的作用有限。虽然也很罕见,但CD36缺乏症在东亚、非洲和阿拉伯血统的个体中患病率相对较高。血小板GP缺乏症患者可产生针对缺失GPs的抗体,导致免疫介导的血小板输注无效(PTR)。因此,他们在最需要血小板输血时无反应。
在此,我们报告一例埃及男性病例,该患者有终身未完全明确的出血性疾病病史,前来接受术前评估。我们诊断该患者为I型Glanzmann血小板无力症。进一步评估发现抗CD36抗体,从而发现同时存在血小板CD36缺乏症。双重GP缺乏症使他的治疗显著复杂化,因为在美国,由于CD36缺乏的献血者罕见,找到交叉配型相容的血小板具有挑战性。
讨论/结论:对并存的血小板疾病及其后果的认识有限,主要是因为这些疾病随机发生且极为罕见(本病例约为一亿分之一)。该病例强调了全面评估血小板糖蛋白缺乏症的重要性,特别是对于患有严重出血性疾病以及来自易患特定血小板疾病种族背景的个体。这种方法可以预防未来血小板抗体的形成,或降低已有抗体时的出血风险。