Evangelidis Paschalis, Gavriilaki Eleni, Kotsiou Nikolaos, Ntova Zacharo, Kalmoukos Panagiotis, Papadopoulou Theodosia, Chissan Sofia, Vakalopoulou Sofia
Second Propaedeutic Department of Internal Medicine, Aristotle University of Thessaloniki, Hippocration Hospital, 54642 Thessaloniki, Greece.
Hematol Rep. 2025 Mar 21;17(2):15. doi: 10.3390/hematolrep17020015.
: Antiphospholipid syndrome (APS) is a systemic autoimmune disease characterized by thrombosis or obstetric complications and the laboratory detection of antiphospholipid antibodies. Although vascular thrombosis is the main manifestation of the disease, other rarer complications have also been described. Avascular necrosis (AN) is considered a rare manifestation of APS. The aim of our case series is to study patients with APS and AN. : A retrospective study was performed on 80 patients diagnosed with APS. : AN was observed in 3 patients out of 80 diagnosed with APS. AN of the femoral head was observed in all cases. Case (1): A 54-year-old woman presented due to multiple ischemic infarctions in the brain, as detected in magnetic resonance imaging of the brain, Raynaud's phenomenon, and AN of the femoral head. In laboratory testing, a prolongation of activated partial thromboplastin time was recorded. A heterozygous mutation was also found in the gene MTHFR C677T, and the patients was positive for lupus anticoagulant (LA). The patient was given clopidogrel and acenocoumarol. Case (2): A 52-year-old man was diagnosed with APS, based on the clinical presentation (stroke) and positivity for LA and anti-β2GPI (anti-β2 glycoprotein I antibody). In his medical history, episodes of vertigo and an episode of AN of the femoral head 2 years ago were described. Case (3): A woman aged 43 years presented due to AN of the femoral head. Due to suspected APS, immunological testing was performed, and positivity for LA and IgM anticardiolipin antibodies was detected. She was treated with acenocoumarol. : AN is a rare clinical manifestation of APS, which may precede the diagnosis of APS for many years.
抗磷脂综合征(APS)是一种全身性自身免疫性疾病,其特征为血栓形成或产科并发症以及抗磷脂抗体的实验室检测阳性。尽管血管血栓形成是该疾病的主要表现,但也有其他较罕见的并发症的报道。无血管性坏死(AN)被认为是APS的一种罕见表现。我们这个病例系列的目的是研究患有APS和AN的患者。:对80例诊断为APS的患者进行了回顾性研究。:在80例诊断为APS的患者中,有3例观察到AN。所有病例均观察到股骨头的AN。病例(1):一名54岁女性因脑部磁共振成像检测到的多发性脑缺血性梗死、雷诺现象和股骨头AN而就诊。实验室检查中,活化部分凝血活酶时间延长。在MTHFR C677T基因中还发现了杂合突变,且患者狼疮抗凝物(LA)阳性。该患者接受了氯吡格雷和醋硝香豆素治疗。病例(2):一名52岁男性根据临床表现(中风)以及LA和抗β2GPI(抗β2糖蛋白I抗体)阳性被诊断为APS。在其病史中,描述了眩晕发作以及2年前的一次股骨头AN发作。病例(3):一名43岁女性因股骨头AN就诊。由于怀疑患有APS,进行了免疫学检测,检测到LA和IgM抗心磷脂抗体阳性。她接受了醋硝香豆素治疗。:AN是APS的一种罕见临床表现,可能在APS诊断前多年就已出现。