Tu Jia-Jie, Wang Jian-Xiong, Xu Sheng-Qian
Key Laboratory of Anti-Inflammatory and Immune Medicine, Ministry of Education, Institute of Clinical Pharmacology, Anhui Collaborative Innovation Center of Anti-Inflammatory and Immune Medicine, Anhui Medical University, Hefei, China.
Department of Rheumatology & Immunology, The First Affiliated Hospital of Anhui Medical University, Hefei, China.
SAGE Open Med Case Rep. 2025 Jun 20;13:2050313X251351769. doi: 10.1177/2050313X251351769. eCollection 2025.
Gout rarely affects the axial joints, and sacroiliac joint involvement is exceptionally uncommon. This report describes the case of a 30-year-old female with a family history of gout who had recurrent knee swelling and low back pain for 2 years, initially misdiagnosed with ankylosing spondylitis. Laboratory findings showed episodic hyperuricemia and elevated inflammatory markers, while MRI revealed bilateral sacroiliitis and bone island in the right sacroiliac joint. HLA-B27 was negative, and no family history of psoriasis or ankylosing spondylitis was noted. The atypical presentation of inflammatory low back pain, along with episodic joint redness, swelling, and pain, prompted further investigation. Dual-energy computed tomography confirmed urate crystal deposition in the sacroiliac joint and knees, accompanied by bone erosion, leading to a final diagnosis of primary sacroiliac joint gout. The patient's symptoms improved significantly after being treated with diclofenac and benzbromarone. This case emphasizes dual-energy computed tomography's diagnostic utility in differentiating gouty arthritis from inflammatory sacroiliitis, especially in patients with atypical presentations, family history of gout, or hyperuricemia. Although rare, axial joint gout should be considered a differential diagnosis for axial and large joint pain. Dual-energy computed tomography provides critical insights, allowing the accurate localization of urate deposits and preventing misdiagnosis or delayed treatment. This case highlights the need for increased clinical awareness and appropriate imaging for rare presentations of gout.
痛风很少累及中轴关节,骶髂关节受累极为罕见。本报告描述了一名30岁女性病例,该患者有痛风家族史,反复出现膝关节肿胀和腰痛2年,最初被误诊为强直性脊柱炎。实验室检查结果显示间歇性高尿酸血症和炎症标志物升高,而磁共振成像(MRI)显示双侧骶髂关节炎以及右侧骶髂关节骨岛形成。人类白细胞抗原B27(HLA-B27)阴性,且无银屑病或强直性脊柱炎家族史。炎性腰痛的非典型表现,以及间歇性关节红肿、疼痛,促使进一步检查。双能计算机断层扫描(双能CT)证实骶髂关节和膝关节有尿酸盐结晶沉积,并伴有骨质侵蚀,最终诊断为原发性骶髂关节痛风。患者接受双氯芬酸和苯溴马隆治疗后症状明显改善。该病例强调了双能CT在鉴别痛风性关节炎与炎性骶髂关节炎方面的诊断效用,尤其是对于非典型表现、有痛风家族史或高尿酸血症的患者。虽然罕见,但中轴关节痛风应被视为中轴关节和大关节疼痛的鉴别诊断之一。双能CT提供了关键的诊断依据,能够准确确定尿酸盐沉积的位置,避免误诊或延误治疗。该病例凸显了提高对痛风罕见表现的临床认识并进行适当影像学检查的必要性。