Preceding Antiphospholipid Syndrome before the Onset of Systemic Lupus Erythematosus Presenting with Iliocaval Deep Vein Thrombosis: A Case Report and Literature Review.

IF 0.6 Q4 PERIPHERAL VASCULAR DISEASE
Annals of vascular diseases Pub Date : 2024-12-25 Epub Date: 2024-10-08 DOI:10.3400/avd.cr.24-00040
Masaya Nakashima, Masayoshi Kobayashi
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引用次数: 0

Abstract

Antiphospholipid syndrome (APS) and systemic lupus erythematosus (SLE) are similar to be characterized by thromboembolic events and various clinical manifestations. We experienced a 21-year-old man with acute iliocaval deep vein thrombosis (DVT). Primary APS was initially diagnosed on the criteria, and after multidisciplinary treatment, iliocaval DVT was gradually regressed. Six months later, the patient complained of acute enteritis, followed by peripheral neuropathy and butterfly lupus. SLE was diagnosed, which suggested that the onset of SLE was preceded by APS. This case raises the question of a present consensus that these two diseases are clearly different clinical entities, although these are closely related.

以髂腔深静脉血栓形成为表现的系统性红斑狼疮发病前的抗磷脂综合征1例报告及文献复习。
抗磷脂综合征(APS)和系统性红斑狼疮(SLE)相似,其特征是血栓栓塞事件和多种临床表现。我们经历了一个21岁的男性急性髂腔深静脉血栓形成(DVT)。原发性APS初步诊断符合标准,经多学科治疗,髂腔DVT逐渐消退。6个月后,患者主诉急性肠炎,接着是周围神经病变和蝴蝶狼疮。诊断为SLE,提示SLE发病前有APS。这个病例提出了一个问题,目前的共识,这两种疾病是明显不同的临床实体,尽管它们是密切相关的。
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来源期刊
Annals of vascular diseases
Annals of vascular diseases PERIPHERAL VASCULAR DISEASE-
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