来历不明的发热——难以捉摸的诊断

Sreekumar H, Gopinath M, Sasidharan S, Joseph Pp
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引用次数: 0

摘要

巨细胞动脉炎(GCA)是一种影响大血管的系统性炎症性疾病。在这里,我们提出的情况下,59岁的男性谁提出了我们的投诉发烧和全身疲劳的6周持续时间。他接受了2个疗程的抗生素治疗,没有任何喘息。外部检查显示红细胞沉降率(ESR)和前列腺特异性抗原(PSA)升高。他被详细评估为FUO。尽管服用了最大剂量的退烧药,他仍持续发烧,高度怀疑是恶性肿瘤。然而,调查没有提示任何恶性肿瘤。入院第3天,患者主诉咀嚼疼痛。检查显示颞动脉突出,脉搏正常,无压痛。眼底检查正常。对颞动脉进行活检,诊断为巨细胞性动脉炎。虽然GCA通常表现为头痛、视觉改变、咀嚼跛行和风湿性多肌痛症状,但在极少数情况下,GCA可能以发烧为唯一的主要症状。没有头痛的GCA是一种罕见的表现,发生在近20%的患者中。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pyrexia of Unknown Origin- An elusive diagnosis
Giant cell arteritis (GCA) is a systemic inflammatory disorder that affects large vessels. Here we present the case of a 59 year old male who presented to us with complaints of fever and generalised tiredness of 6 weeks duration. He had received 2 courses of antibiotics with no respite. Investigations from outside showed elevated erythrocyte sedimentation rate (ESR) and prostate specific antigen (PSA). He was evaluated in detail as FUO. His fever persisted despite maximal dose of antipyretics, leading to high suspicion of malignancy. However, investigations were not suggestive of any malignancy. On day 3 of admission, he complained of pain on mastication. Examination revealed prominent temporal arteries, with normal pulsations without any tenderness. Fundus examination was normal. With high index of suspicion, temporal artery was biopsied and was diagnostic of giant cell arteritis. Though GCA classically presents with headache, visual changes, masticatory claudication, and symptoms of polymyalgia rheumatica, on rare occasion, GCA may present with fever as the only dominant symptom. GCA without headache is an uncommon presentation, which occurs in nearly 20% of patients.
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