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一名患有基础感染、免疫性血小板减少性紫癜(ITP)和多发性硬化症患者的血小板卫星现象

Platelet Satellitism in a Patient with Underlying Infection, Immune Thrombocytopenic Purpura (ITP) and Multiple Sclerosis.

作者信息

Liaskas Athanasios, El-Gkotmi Natali, Karapaschalidis Anestis, Tzanetakos Dimitrios, Valsami Serena

机构信息

Hematology Laboratory and Blood Bank, Aretaieion Hospital, National and Kapodistrian University of Athens, 11528 Athens, Greece.

Second Department of Neurology, "Attikon" University Hospital, School of Medicine, National and Kapodistrian University of Athens, 12461Athens, Greece.

出版信息

Diagnostics (Basel). 2025 May 24;15(11):1319. doi: 10.3390/diagnostics15111319.

Abstract

Platelet satellitism (PS) is an in vitro phenomenon of platelets adhering around white blood cells, especially in blood samples anticoagulated with KEDTA. This, in some cases, can lead to spurious thrombocytopenia, without platelet dysfunction or bleeding events. Diagnosis is made by peripheral blood smear examination. The potential mechanism for PS remains largely unknown; however, it possibly involves the formation of IgG antibodies against the platelet glycoprotein receptor IIb/IIIa (GPIIb/IIIa). PS has been observed in various medical conditions, including infectious, autoimmune, and lymphoproliferative disorders, without an obvious causative relationship. Here, we describe a case of PS in a patient who presented with infection in the setting of underlying Immune Thombocytopenic Purpura and Multiple Sclerosis.

摘要

血小板卫星现象(PS)是一种血小板在白细胞周围黏附的体外现象,尤其在使用乙二胺四乙酸钾(KEDTA)抗凝的血样中。在某些情况下,这可能导致假性血小板减少,而无血小板功能障碍或出血事件。通过外周血涂片检查进行诊断。PS的潜在机制在很大程度上仍不清楚;然而,它可能涉及针对血小板糖蛋白受体IIb/IIIa(GPIIb/IIIa)的IgG抗体的形成。PS已在各种医学病症中观察到,包括感染性、自身免疫性和淋巴增殖性疾病,但无明显因果关系。在此,我们描述一例血小板卫星现象病例,该患者在患有基础免疫性血小板减少性紫癜和多发性硬化症的情况下出现感染。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b0cb/12155310/f913e1e01a54/diagnostics-15-01319-g001.jpg

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