Antiphospholipid syndrome: a case report with an unusual wide spectrum of clinical manifestations.

Q1 Medicine
Auto-Immunity Highlights Pub Date : 2019-10-19 eCollection Date: 2019-12-01 DOI:10.1186/s13317-019-0119-3
Carmela Mazzoccoli, Domenico Comitangelo, Alessia D'Introno, Valeria Mastropierro, Carlo Sabbà, Antonio Perrone
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引用次数: 2

Abstract

Background: Antiphospholipid syndrome (APS) is an autoimmune disease characterized by the occurrence of venous and/or arterial thrombosis, and the detection of circulating antiphospholipid antibodies. The classification criteria for definite APS are actually met when at least one clinical criterion (thrombosis or pregnancy morbidity) is present in association of one laboratory criterion (LAC, aCL antibody or aβ2GPI antibody present on two or more occasions, at least 12 weeks a part), and thrombosis should be confirmed by objective validated criteria. The average age of primary APS patients has been reported to be about 35-40 years and the disease is more common in women than in men.

Case presentation: In this report, we described a rare case of an adult male who presented over a period of 9 years with a wide spectrum of clinical manifestations involving different organs that were not initially diagnosed as APS. Dizziness and syncope were his first clinical symptoms, and a non-bacterial thrombotic endocarditis (NBTE) involving the mitral valve was at first diagnosed. Subsequently, the patient also presented with generalized seizures and subsequent head injury. When the patient was admitted to our clinic with bilateral epistaxis and fever, thrombocytopenia was revealed. Moreover, laboratory examinations showed acute pancreatitis with an increase of levels of inflammation markers.

Conclusion: Based on the patient's medical history and all the examination results, it was possible to make a diagnosis of primary APS and, starting from diagnosis of thrombocytopenia, we were allowed to conclude that all of manifestation were epi-phenomena of a unique clinical entity, rather than unrelated diseases. Though APS is one of the most common thrombocytophilias, unfortunately, it is not recognized often enough. The lack of prevention in undiagnosed patients may cause severe complications which can in turn result in the death of those patients.

抗磷脂综合征:一个异常广泛的临床表现的病例报告。
背景:抗磷脂综合征(APS)是一种以静脉和/或动脉血栓形成和循环抗磷脂抗体检测为特征的自身免疫性疾病。当至少有一项临床标准(血栓形成或妊娠发病率)与一项实验室标准(LAC、aCL抗体或aβ 2gpi抗体出现两次或两次以上,每次至少12周)相关联,并且血栓形成应通过客观验证的标准确认时,才符合明确APS的分类标准。据报道,原发性APS患者的平均年龄约为35-40岁,女性比男性更常见。病例介绍:在本报告中,我们描述了一个罕见的成年男性病例,他在9年的时间里出现了广泛的临床表现,涉及不同的器官,最初并没有被诊断为APS。他的第一个临床症状是头晕和晕厥,最初诊断为累及二尖瓣的非细菌性血栓性心内膜炎(NBTE)。随后,患者还出现全身性癫痫发作和随后的头部损伤。当患者因双侧鼻出血和发热而入院时,发现血小板减少症。此外,实验室检查显示急性胰腺炎,炎症标志物水平升高。结论:根据患者的病史和所有的检查结果,可以诊断为原发性APS,从血小板减少的诊断开始,我们可以得出所有的表现都是一个独特的临床实体的外显现象,而不是不相关的疾病。虽然APS是最常见的血小板增多症之一,不幸的是,它不经常被认识到。对未确诊患者缺乏预防可能导致严重并发症,进而导致这些患者死亡。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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