Internal Medicine, Parkview Medical Center, Pueblo, Colorado, USA.
Internal Medicine, Parkview Medical Center, Pueblo, Colorado, USA
BMJ Case Rep. 2021 Mar 26;14(3):e239713. doi: 10.1136/bcr-2020-239713.
Fever of unknown origin (FUO) has a broad differential diagnosis, including infectious, inflammatory and malignant aetiologies. Granulomatosis with polyangiitis (GPA) can present with non-specific symptoms, including fever, lethargy and flu-like illness. While systemic vasculitis causing FUO has been well-documented, GPA as an underlying cause for FUO poses a diagnostic and therapeutic challenge for clinicians. We present the case of a 65-year-old man who presented to the emergency department with a report of fever, myalgia and night sweats for greater than 3 weeks. After an extensive workup, the patient was diagnosed with GPA and he eventually responded to corticosteroids and immunosuppressive therapy. This case aims to raise awareness of FUO secondary to GPA and serves as a reminder to clinicians that early recognition and prompt treatment of this syndrome improves patient outcomes.
不明原因发热(FUO)有广泛的鉴别诊断,包括感染性、炎症性和恶性病因。肉芽肿伴多血管炎(GPA)可表现为非特异性症状,包括发热、乏力和流感样疾病。虽然导致 FUO 的系统性血管炎已有充分记载,但 GPA 作为 FUO 的潜在原因对临床医生来说是一个诊断和治疗上的挑战。我们报告了一例 65 岁男性患者,他因发热、肌痛和盗汗超过 3 周而到急诊科就诊。经过广泛的检查,该患者被诊断为 GPA,最终对皮质类固醇和免疫抑制治疗有反应。本病例旨在提高对 GPA 引起的 FUO 的认识,并提醒临床医生,早期识别和及时治疗这种综合征可改善患者的预后。