多形核白细胞吞噬血小板导致假性血小板减少症

IF 10.1 1区 医学 Q1 HEMATOLOGY American Journal of Hematology Pub Date : 2024-12-16 DOI:10.1002/ajh.27562
Iliana Stamatiou, Zoe Bezirgiannidou, Evangelia Charitaki, Ioannis Kotsianidis, Konstantinos Liapis
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Of 200 neutrophils examined, 161 (80%) contained between one and six platelets (Figure 1). These findings indicated spurious thrombocytopenia. The emergency department staff were notified by the laboratory that the patient's platelet count was normal. Subsequently, she underwent internal jugular-vein catheterization for fluid resuscitation without oozing or hematoma. Pseudomembranous colitis was diagnosed on the basis of a positive <i>Clostridioides difficile</i> stool test. She was treated with metronidazole and vancomycin, but her course was complicated by renal failure necessitating hemodialysis. Eventually, she made a full recovery. During hospitalization, multiple routinely prepared films from EDTA-anticoagulated blood consistently demonstrated platelet phagocytosis but with the resolution of the colitis, the phenomenon became progressively less pronounced. The automated platelet count became normal within 30 days.</p>\n<figure><picture>\n<source media=\"(min-width: 1650px)\" srcset=\"/cms/asset/43ba7b26-cdb9-4a52-851b-76e271182229/ajh27562-fig-0001-m.jpg\"/><img alt=\"Details are in the caption following the image\" data-lg-src=\"/cms/asset/43ba7b26-cdb9-4a52-851b-76e271182229/ajh27562-fig-0001-m.jpg\" loading=\"lazy\" src=\"/cms/asset/533e4fe2-c86d-4138-a00c-28ff5b938961/ajh27562-fig-0001-m.png\" title=\"Details are in the caption following the image\"/></picture><figcaption>\n<div><strong>FIGURE 1<span style=\"font-weight:normal\"></span></strong><div>Open in figure viewer<i aria-hidden=\"true\"></i><span>PowerPoint</span></div>\n</div>\n<div>Four fields of the peripheral-blood smear, showing ingestion of platelets by neutrophilic granulocytes (May-Grünwald-Giemsa stain, ×1000).</div>\n</figcaption>\n</figure>\n<p>A peripheral-blood smear should always be examined in new cases of thrombocytopenia or whenever the platelet count is unexpectedly low, in order to confirm the thrombocytopenia. The blood smear may be requested by physicians or initiated by laboratory staff [<span>1</span>]. As seen here, a laboratory-initiated blood smear, is particularly valuable because it may permit earlier recognition of pseudothrombocytopenia. The incidence of pseudothrombocytopenia is 1.9% among hospitalized patients and 0.15% in the outpatient setting [<span>2</span>]. Falsely low counts may be the result of small clots, platelet clumping, platelet satellitism, or abnormally large platelets. Phagocytosis of platelets by neutrophilic granulocytes is a rare cause of pseudothrombocytopenia, often seen in association with platelet satellitism [<span>2</span>]. Ordinarily, “flags” produced by automated blood-count analyzers are very useful for detecting errors in platelet enumeration. In this patient, however, the flagging system did not detect an error, suggesting that phagocytosis of platelets by neutrophils cannot be detected by the automated flagging systems.</p>\n<p>Phagocytosis of platelets by neutrophilic granulocytes is an in vitro phenomenon occurring only in EDTA-anticoagulated blood [<span>2, 3</span>]. It is not reproduced if blood is drawn into a citrated tube or smears are made directly from capillary blood. The underlying mechanism is not fully understood, but might be related to IgG autoantibodies directed against the glycoprotein IIb/IIIa complex of platelets and the Fcγ-receptor III of neutrophils. The working hypothesis is that at room temperature, the chelation of calcium ions by EDTA alters the glycoprotein IIb/IIIa molecule and the neutrophil Fcγ-receptor exposing epitopes for the IgG autoantibody, which forms a bridge between platelets and neutrophils. Neutrophil–platelet adherence is followed by platelet phagocytosis [<span>2, 3</span>]. 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On evaluation, she was in clinical shock, with blood pressure 88/58 mmHg and heart rate 122 beats per minute. A complete blood count provided by the Sysmex XN-1000 analyzer showed leukocytosis (13.8 × 10<sup>9</sup>/L, 95% neutrophils) and thrombocytopenia (22 × 10<sup>9</sup>/L). She had acidosis, renal impairment, coagulopathy, and elevated C-reactive protein level. Because of the thrombocytopenia, an examination of a peripheral-blood smear was performed in the hematology laboratory, which showed vacuolated neutrophils that contained phagocytized platelets. Of 200 neutrophils examined, 161 (80%) contained between one and six platelets (Figure 1). These findings indicated spurious thrombocytopenia. The emergency department staff were notified by the laboratory that the patient's platelet count was normal. Subsequently, she underwent internal jugular-vein catheterization for fluid resuscitation without oozing or hematoma. Pseudomembranous colitis was diagnosed on the basis of a positive <i>Clostridioides difficile</i> stool test. She was treated with metronidazole and vancomycin, but her course was complicated by renal failure necessitating hemodialysis. Eventually, she made a full recovery. During hospitalization, multiple routinely prepared films from EDTA-anticoagulated blood consistently demonstrated platelet phagocytosis but with the resolution of the colitis, the phenomenon became progressively less pronounced. 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引用次数: 0

摘要

一名75岁女性因呼吸道感染服用左氧氟沙星后出现进行性腹痛、发热和腹泻,被送往急诊科。经评估,她处于临床休克状态,血压88/58 mmHg,心率每分钟122次。Sysmex XN-1000分析仪提供的全血细胞计数显示白细胞增多(13.8 × 109/L, 95%中性粒细胞)和血小板减少(22 × 109/L)。她有酸中毒、肾功能损害、凝血功能障碍和c反应蛋白水平升高。由于血小板减少,在血液学实验室进行外周血涂片检查,显示空泡中性粒细胞含有被吞噬的血小板。在检测的200个中性粒细胞中,161个(80%)含有1 - 6个血小板(图1)。这些结果提示假性血小板减少症。急诊科的工作人员接到化验室的通知,病人的血小板计数正常。随后,她接受颈内静脉置管进行液体复苏,无渗出或血肿。假膜性结肠炎是在艰难梭菌粪便试验阳性的基础上诊断的。她接受了甲硝唑和万古霉素的治疗,但她的病程因肾功能衰竭而复杂化,需要进行血液透析。最后,她完全康复了。住院期间,多次常规制备的edta抗凝血片一致显示血小板吞噬,但随着结肠炎的消退,这种现象逐渐不明显。自动血小板计数在30天内恢复正常。图1打开图形查看器powerpoint4场外周血涂片,显示嗜中性粒细胞摄取血小板(may - gr nwald- giemsa染色,×1000)。在血小板减少的新病例或血小板计数异常低的情况下,外周血涂片应经常检查,以确认血小板减少。血液涂片可由医生要求或由实验室工作人员发起。如图所示,实验室发起的血液涂片特别有价值,因为它可以早期识别假性血小板减少症。假性血小板减少症的发生率在住院患者中为1.9%,在门诊患者中为0.15%。虚低计数可能是小血块、血小板结块、血小板卫星化或血小板异常大的结果。嗜中性粒细胞吞噬血小板是一种罕见的假性血小板减少症的病因,通常与血小板卫星性[2]有关。通常,自动血液计数分析仪产生的“标志”对于检测血小板计数错误非常有用。然而,在这个病人中,标记系统没有检测到错误,这表明中性粒细胞对血小板的吞噬不能被自动标记系统检测到。嗜中性粒细胞吞噬血小板是一种体外现象,仅发生在edta抗凝血中[2,3]。如果将血液抽入柠檬酸管或直接从毛细血管血液中涂片,则无法复制。其潜在机制尚不完全清楚,但可能与针对血小板糖蛋白IIb/IIIa复合物和中性粒细胞fc γ-受体III的IgG自身抗体有关。工作假设是,在室温下,EDTA对钙离子的螯合作用改变了糖蛋白IIb/IIIa分子和暴露IgG自身抗体的中性粒细胞fc γ-受体表位,从而在血小板和中性粒细胞之间形成了一座桥梁。中性粒细胞-血小板粘附之后是血小板吞噬[2,3]。血小板活化也可能起一定作用。在炎症触发的激活下,血小板在其表面表达p -选择素,这有助于血小板粘附中性粒细胞[4]。与常规血球计数中经常发生的血小板聚集相反,血小板吞噬主要见于严重疾病,如感染、血栓形成和恶性高血压[3]。我们的病人的情况下,据我们所知,假性血小板减少发生在假性膜性结肠炎的第一份报告。这个病例说明了急性病人的假性血小板减少症的一个重要原因。认识到这一现象可以防止不必要的措施,如血小板输注、推迟侵入性干预或停药。
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Pseudothrombocytopenia due to Phagocytosis of Platelets by Polymorphonuclear Leukocytes

A 75-year-old woman presented to the emergency department with progressive abdominal pain, fever, and diarrhea after taking levofloxacin for a respiratory tract infection. On evaluation, she was in clinical shock, with blood pressure 88/58 mmHg and heart rate 122 beats per minute. A complete blood count provided by the Sysmex XN-1000 analyzer showed leukocytosis (13.8 × 109/L, 95% neutrophils) and thrombocytopenia (22 × 109/L). She had acidosis, renal impairment, coagulopathy, and elevated C-reactive protein level. Because of the thrombocytopenia, an examination of a peripheral-blood smear was performed in the hematology laboratory, which showed vacuolated neutrophils that contained phagocytized platelets. Of 200 neutrophils examined, 161 (80%) contained between one and six platelets (Figure 1). These findings indicated spurious thrombocytopenia. The emergency department staff were notified by the laboratory that the patient's platelet count was normal. Subsequently, she underwent internal jugular-vein catheterization for fluid resuscitation without oozing or hematoma. Pseudomembranous colitis was diagnosed on the basis of a positive Clostridioides difficile stool test. She was treated with metronidazole and vancomycin, but her course was complicated by renal failure necessitating hemodialysis. Eventually, she made a full recovery. During hospitalization, multiple routinely prepared films from EDTA-anticoagulated blood consistently demonstrated platelet phagocytosis but with the resolution of the colitis, the phenomenon became progressively less pronounced. The automated platelet count became normal within 30 days.

Details are in the caption following the image
FIGURE 1
Open in figure viewerPowerPoint
Four fields of the peripheral-blood smear, showing ingestion of platelets by neutrophilic granulocytes (May-Grünwald-Giemsa stain, ×1000).

A peripheral-blood smear should always be examined in new cases of thrombocytopenia or whenever the platelet count is unexpectedly low, in order to confirm the thrombocytopenia. The blood smear may be requested by physicians or initiated by laboratory staff [1]. As seen here, a laboratory-initiated blood smear, is particularly valuable because it may permit earlier recognition of pseudothrombocytopenia. The incidence of pseudothrombocytopenia is 1.9% among hospitalized patients and 0.15% in the outpatient setting [2]. Falsely low counts may be the result of small clots, platelet clumping, platelet satellitism, or abnormally large platelets. Phagocytosis of platelets by neutrophilic granulocytes is a rare cause of pseudothrombocytopenia, often seen in association with platelet satellitism [2]. Ordinarily, “flags” produced by automated blood-count analyzers are very useful for detecting errors in platelet enumeration. In this patient, however, the flagging system did not detect an error, suggesting that phagocytosis of platelets by neutrophils cannot be detected by the automated flagging systems.

Phagocytosis of platelets by neutrophilic granulocytes is an in vitro phenomenon occurring only in EDTA-anticoagulated blood [2, 3]. It is not reproduced if blood is drawn into a citrated tube or smears are made directly from capillary blood. The underlying mechanism is not fully understood, but might be related to IgG autoantibodies directed against the glycoprotein IIb/IIIa complex of platelets and the Fcγ-receptor III of neutrophils. The working hypothesis is that at room temperature, the chelation of calcium ions by EDTA alters the glycoprotein IIb/IIIa molecule and the neutrophil Fcγ-receptor exposing epitopes for the IgG autoantibody, which forms a bridge between platelets and neutrophils. Neutrophil–platelet adherence is followed by platelet phagocytosis [2, 3]. Platelet activation may also play a part. On activation by inflammatory triggers, platelets express P-selectin on their surfaces, which facilitates platelet adherence to neutrophils [4].

In contrast to platelet clumping which frequently occurs in routine blood counts, platelet phagocytosis is seen mainly during severe illness such as infection, thrombosis, and malignant hypertension [3]. Our patient's case is, to our knowledge, the first report of pseudothrombocytopenia occurring in pseudomembranous colitis.

This case illustrates an important cause of spurious thrombocytopenia in the acutely ill patient. Awareness of this phenomenon can prevent unnecessary measures such as platelet transfusions, postponement of invasive interventions, or discontinuation of medications.

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来源期刊
CiteScore
15.70
自引率
3.90%
发文量
363
审稿时长
3-6 weeks
期刊介绍: The American Journal of Hematology offers extensive coverage of experimental and clinical aspects of blood diseases in humans and animal models. The journal publishes original contributions in both non-malignant and malignant hematological diseases, encompassing clinical and basic studies in areas such as hemostasis, thrombosis, immunology, blood banking, and stem cell biology. Clinical translational reports highlighting innovative therapeutic approaches for the diagnosis and treatment of hematological diseases are actively encouraged.The American Journal of Hematology features regular original laboratory and clinical research articles, brief research reports, critical reviews, images in hematology, as well as letters and correspondence.
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