Painful unilateral facial swelling due to superficial temporal artery thrombosis: a rare presentation of Antiphospholipid Syndrome

Helena da Cunha Lopes de Lima, Ana Clara Dias Pereira, Naiara Cunha de Moura, V. L. Silva, Hilton Mariano da Silva Júnior
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Abstract

Introduction Persistent painful unilateral temporal swelling is rarely seen in clinical practice. Antiphospholipid syndrome (APS) is an autoimmune and systemic disorder that causes changes in blood clotting homeostasis, marked by arterial or venous thrombosis, gestational morbidity, and high and persistently positive serum levels of antiphospholipid antibodies (aPL). APS is more common in young women and middle-aged adults, with no preference for race. Among its clinical features, temporal artery thrombosis, associated with headache and temporal and hemifacial edema is extremely rare, with few publications worldwide on this topic. Objective This report aims to present the case of a unilateral painful facial edema due to thrombosis of the superficial temporal artery as an unprecedented manifestation of Antiphospholipid Syndrome. Thus, the only record in the English-language literature surveyed in the Pubmed database in July 2022 highlights the rarity of this APS presentation and the consequent challenge in suspecting the correct diagnosis for adequate treatment. Methods  Case report. Data disclosure was authorized by the patient through an informed consent form. Results A 32-year-old woman was presented with pain in the right temporal region of her face. The pain was intense, daily and continuous, pulsating, without irradiation, which worsened with physical activity and presented partial relief with common analgesics. After 20 days, she developed a right pale temporal edema (Figure 1) associated with a significant worsening of pain and intense right unilateral headache attacks triggered by chewing and speaking. She has a history of deep vein thrombosis in the left lower limb. Physical examination and imaging tests showed significant cold edema of the right temporal region with asymmetry of the temporal muscles, which was extremely painful on palpation and made it difficult to open the mouth. There were no other changes in the general physical... (Too see the complete abstract, please, check out the PDF.)
由于颞浅动脉血栓形成引起的疼痛的单侧面部肿胀:抗磷脂综合征的罕见表现
在临床实践中,持续疼痛的单侧颞肿胀是罕见的。抗磷脂综合征(APS)是一种自身免疫性和全身性疾病,可引起血液凝血稳态的改变,其特征是动脉或静脉血栓形成、妊娠发病率、血清抗磷脂抗体(aPL)水平高且持续阳性。APS在年轻女性和中年人中更常见,没有种族偏好。在其临床特征中,颞动脉血栓形成与头痛、颞部和半面水肿相关极为罕见,世界范围内关于该主题的出版物很少。目的本报告的目的是提出一个病例单侧疼痛的面部水肿由于颞浅动脉血栓形成的一个前所未有的抗磷脂综合征的表现。因此,2022年7月在Pubmed数据库中调查的英语文献中唯一的记录突出了这种APS表现的罕见性以及随之而来的怀疑正确诊断以进行适当治疗的挑战。方法病例报告。数据披露由患者通过知情同意书授权。结果一名32岁女性患者表现为面部右侧颞区疼痛。疼痛剧烈,每日持续,搏动,无照射,随体力活动加重,常用镇痛药部分缓解。20天后,患者出现右侧浅颞水肿(图1),疼痛明显加重,咀嚼和说话引发右侧剧烈单侧头痛发作。她有左下肢深静脉血栓的病史。体格检查及影像学检查显示右侧颞区明显冷水肿,颞肌不对称,触诊极度疼痛,难以开口。总的身体没有其他变化……(也可以查看完整的摘要,请查看PDF。)
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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