Crowned Dens Syndrome Mimicking Atlantoaxial Infection in a Patient With Systemic Sclerosis: A Case Report.

Case Reports in Rheumatology Pub Date : 2026-02-22 eCollection Date: 2026-01-01 DOI:10.1155/crrh/3673141
Tarun Selvarajan, Lavanya Kannekanti, Shravya Balmuri, Samina Hayat
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Abstract

Objective: Crowned dens syndrome (CDS), caused by calcium pyrophosphate or hydroxyapatite deposition around the odontoid process, is an under-recognized cause of acute severe neck pain and headache. It can closely mimic septic arthritis, osteomyelitis, giant cell arteritis (GCA), polymyalgia rheumatica (PMR), or cervical spondylitis. We report a case of CDS in a patient with diffuse systemic sclerosis initially managed for presumed infection.

Methods: A 55-year-old man with diffuse cutaneous systemic sclerosis on mycophenolate mofetil and methotrexate presented with severe throbbing headache, facial tenderness, and diffuse pain. CT/CTA of the head and neck were negative for vascular events; MRI revealed inflammatory changes at the atlantoaxial and atlanto-occipital joints concerning for septic arthritis/osteomyelitis with abscess formation. Broad-spectrum antibiotics were initiated.

Results: The patient's symptoms persisted despite antibiotics, prompting repeat imaging. CT demonstrated calcifications surrounding the odontoid process, raising suspicion for CDS. Colchicine and low-dose prednisone were introduced while antibiotics were continued, given ongoing concern for occult infection in an immunosuppressed host. Within 1 week, the patient experienced near-complete resolution of pain. At follow-up, he remained symptom-free, allowing reintroduction of methotrexate while mycophenolate was held.

Conclusion: CDS should be considered in the differential diagnosis of severe headache and neck pain in rheumatology patients, particularly when imaging shows craniocervical inflammation and calcifications. CT of the odontoid is diagnostic, but MRI findings may mimic infection. Awareness of CDS is critical to avoid misdiagnosis, unnecessary procedures, or prolonged inappropriate therapy. Prompt recognition and anti-inflammatory treatment can be rapidly effective and permit safe reintroduction of disease-modifying therapy.

冠齿综合征在系统性硬化症患者中模拟寰枢关节感染:一例报告。
目的:冠状突综合征(CDS)是由齿状突周围焦磷酸钙或羟基磷灰石沉积引起的,是急性严重颈部疼痛和头痛的一个未被充分认识的原因。它可以近似模拟脓毒性关节炎、骨髓炎、巨细胞动脉炎(GCA)、风湿性多肌痛(PMR)或颈椎炎。我们报告一例弥漫性系统性硬化症患者的CDS,最初因假定感染而进行治疗。方法:一名55岁男性,因服用霉酚酸酯和甲氨蝶呤导致弥漫性皮肤系统性硬化症,表现为剧烈的搏动性头痛、面部压痛和弥漫性疼痛。头颈部CT/CTA未见血管事件;MRI显示寰枢关节和寰枕关节的炎症改变与脓毒性关节炎/骨髓炎伴脓肿形成有关。开始使用广谱抗生素。结果:尽管使用抗生素,患者的症状仍持续存在,促使患者重复影像学检查。CT显示齿状突周围有钙化,怀疑为CDS。在继续使用抗生素的同时,引入秋水仙碱和低剂量强的松,考虑到免疫抑制宿主的隐性感染。在1周内,患者经历了几乎完全的疼痛缓解。在随访中,他仍然没有症状,允许重新引入甲氨蝶呤,同时保留麦考酚酸酯。结论:在风湿病患者严重头痛和颈部疼痛的鉴别诊断中应考虑CDS,特别是当影像学显示颅颈炎症和钙化时。齿状突的CT是诊断性的,但MRI的结果可能模拟感染。意识到CDS对于避免误诊、不必要的程序或延长不适当的治疗是至关重要的。及时识别和抗炎治疗可迅速有效,并允许安全重新引入疾病改善治疗。
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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