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27 August 2024: Articles  China

Acute Neck Pain from Crowned Dens Syndrome: A Case Report and Clinical Insights

Challenging differential diagnosis, Unusual or unexpected effect of treatment, Rare disease

Lin Xie ORCID logo1ABCDEFG*, Hanmo Fang1ACEF, Chenpeng Dong ORCID logo1ABCDE, Min Cui1ABCDE, Kangcheng Zhao1ABCDE, Cao Yang1ABCDEF, Xinghuo Wu1ABCDEFG

DOI: 10.12659/AJCR.944684

Am J Case Rep 2024; 25:e944684

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Abstract

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BACKGROUND: Crowned dens syndrome (CDS) is a rare condition characterized by deposition of calcium pyrophosphate crystals on the odontoid process of the second cervical vertebra, forming a calcified ‘crown’, with neck pain being a common symptom. The disorder exhibits unique clinical and radiological features, resembling manifestations of meningitis, such as acute headaches and cervical stiffness. There are few case reports and case series related to CDS. Patients generally respond well to treatment with nonsteroidal anti-inflammatory drugs (NSAIDs), although there is a certain rate of recurrence. Since there are few reports of CDS, we sought to publish this case report, aiming of increasing clinicians’ awareness and reducing misdiagnosis rates.

CASE REPORT: A 62-year-old man presented to the Emergency Department with “cutting-like” headaches and neck pain for 2 days, and was subsequently diagnosed with CDS by cervical computed tomography (CT) scan, and hematological tests revealed inflammatory manifestations. He was advised to take oral nonsteroidal anti-inflammatory drugs and to rest; his symptoms improved after 3 days and his neck pain had almost resolved after 2 months.

CONCLUSIONS: In older patients experiencing new headaches and neck pain, along with increased inflammatory markers, particularly those with a history of pseudogout, the possibility of CDS should be considered. Case reports suggest that oral NSAIDs and short courses of corticosteroids can generally alleviate symptoms. Further research is needed on CDS diagnosis and treatment.

Keywords: Calcium Pyrophosphate, Chondrocalcinosis 2, Neck Pain, Calcification, Physiologic

Introduction

Crowned dens syndrome, also known as calcium pyrophosphate deposition disease, has a reported prevalence of 15% among individuals aged 65–74 years, with no sex differences [1]. If calcification of the cartilage occurs in the ligaments around the odontoid process, it can result in either years of asymptomatic behavior or acute episodes of headaches and neck pain, mimicking the symptoms of meningitis (eg, fever, severe pain, acute onset) [2]. CDS can cause acute cervical pain, more commonly in females (60%) [3,4]. First described in 1985 [2], the syndrome is most prevalent in individuals over the age of 60. The pathological basis is a metabolic disorder characterized by the deposition of calcium pyrophosphate crystals around the odontoid process of the C1 and C2 cervical vertebrae and the surrounding transverse ligaments [5]. Blood tests usually reveal elevated markers of inflammation [6]. Conventionally, NSAIDs have been regarded as the first-line drugs for CDS [7]. It was found that nonsteroidal anti-inflammatory drugs and prednisolone in combination were most effective and thus are the recommended treatment [4,7,8].

If misdiagnosed as an infection, invasive cervical procedures may be performed by physicians, whereas conservative treatment is actually the best approach [9]. This article presents a case of a 62-year-old man with CDS with acute headache and neck pain, to increase clinicians’ awareness and reduce mis-diagnosis rates.

Case Report

A 62-year-old man with a medical history of hypertension and hyperlipidemia presented to the Emergency Department with “cutting-like” headaches and neck pain for 2 days. The preliminary examination revealed that his blood pressure was 155/85 mmHg, body temperature was 37.2°C, and heart rate was 74 beats/min. Physical examination also revealed a soft cervical spine with limited range of motion and no neurological signs. A cervical computed tomography (CT) scan and hematological tests were recommended. Test results indicated leukocyte count of 12 000/µl and C-reactive protein levels of 53.1 mg/dl. CT findings showed linear calcification around the odontoid process, suggesting CDS (Figure 1). The patient was advised to take oral nonsteroidal anti-inflammatory drugs and to rest, and his symptoms improved after 3 days. A 2-month follow-up in the outpatient clinic revealed that his neck pain had almost completely resolved.

Discussion

CDS was first reported by Bouvet in 1985 and is most common in individuals over the age of 60 [10]. It presents as mild to severe pain in the neck and shoulders, accompanied by occipital headaches [11]. Patients often experience short-term fever, exacerbated neck pain, and headaches [12]. The condition is more common in females and is associated with pseudogout, hyperparathyroidism, hemochromatosis, and hypophosphatasia [13]. However, Koyfman et al reported on a 53-year-old woman with CDS who did not have inflammatory indicators [14], suggesting that our consideration for CDS needs to be more extensive.

The pathological basis involves deposition of calcium pyrophosphate or hydroxyapatite crystals in and around the odontoid process, synovial membranes, joint capsules, transverse ligaments, cruciate ligaments, and alar ligaments [15]. While usually asymptomatic, it can trigger further non-specific inflammatory responses, leading to attachment of various protein molecules to its surface. Neutrophils phagocytose these protein complexes, causing an inflammatory response and the release of proteolytic enzymes that erode the ligamentous tissue, further exacerbating the inflammation [16]. The pathophysiological mechanisms behind the deposition of calcium pyrophosphate or hydroxyapatite are not yet fully understood.

Imaging diagnosis can be confirmed through a cervical CT scan, making it crucial to suspect this diagnosis and perform a cervical CT scan accordingly [12]. The syndrome is frequently misdiagnosed as several other conditions, including cervical trauma, meningitis, osteomyelitis, intervertebral disc infection, and fever of unknown origin. Importantly, it is necessary to perform a cervical CT scan during the acute phase; otherwise, the calcification may be absorbed, making it difficult to diagnose CDS on subsequent scans [17]. Therefore, multiple follow-up examinations are recommended.

Complications of CDS include persistent degeneration of the atlantoaxial joint, ligamentous erosion leading to atlantoaxial instability, and atlantoaxial dislocation resulting in spinal cord compression [18]. Overall, the prognosis in these reported cases is generally good. During acute episodes, treatment with nonsteroidal anti-inflammatory drugs (NSAIDs) is recommended for 2–3 weeks. If symptoms do not significantly improve, a short course of corticosteroids can usually alleviate the condition. To date, no medications have been developed to eliminate existing crystal deposits in the ligaments or to prevent their formation, so the focus of treatment is on reducing the associated inflammation. Low-dose colchicine has been suggested as a long-term treatment option to prevent recurrence of CDS [9]. For long-term cases leading to atlantoaxial dislocation and spinal cord compression with resultant neurological decline, surgical decompression and internal fixation fusion are the primary treatment options [18].

Koyfman et al reported a case of CDS in which a patient had occipital pain and calcified deposits in the alar ligament, while our patient had head and neck pain and linear calcification around the odontoid process. There are subtle differences in the location of calcification between the 2 cases, and their patient did not have inflammatory symptoms, but our patient had obvious inflammatory symptoms – elevated body temperature, C-reactive protein, and white blood cells [14]. Comparison of these 2 cases shows that the location of calcification and the presence or absence of inflammatory response adds great difficulty to the diagnosis of CDS. When dealing with cases of pericervical pain, the possibility of CDS should be considered.

Conclusions

For older patients presenting with new-onset headaches and neck pain accompanied by elevated inflammatory markers, especially those with a history of pseudogout, the possibility of CDS should be considered. A cervical CT scan is the preferred initial investigation to avoid unnecessary lumbar punctures as well as antibiotic or antiviral treatments. To date, there have been no large-scale clinical studies for follow-up treatment of this disease. However, data from case reports suggest that oral NSAIDs and short courses of corticosteroids can generally alleviate symptoms.

References:

1.. Abhishek A, Tedeschi SK, Pascart T, The 2023 ACR/EULAR classification criteria for calcium pyrophosphate deposition disease: Ann Rheum Dis, 2023; 82(10); 1248-57

2.. Bouvet JP, le Parc JM, Michalski B, Acute neck pain due to calcifications surrounding the odontoid process: The crowned dens syndrome: Arthritis Rheum, 1985; 28(12); 1417-20

3.. Chang EY, Lim WY, Wolfson T, Frequency of atlantoaxial calcium pyrophosphate dihydrate deposition at CT: Radiology, 2013; 269(2); 519-24

4.. Goto S, Umehara J, Aizawa T, Kokubun S, Crowned dens syndrome: J Bone Joint Surg Am, 2007; 89(12); 2732-36

5.. Abhishek A, Tedeschi SK, Pascart T, The 2023 ACR/EULAR classification criteria for calcium pyrophosphate deposition disease: Arthritis Rheumatol, 2023; 75(10); 1703-13

6.. Kurihara M, Tokuda Y, Jolt accentuation of neck pain: A novel physical finding for crowned dens syndrome: BMJ Case Rep, 2016; 2016; bcr2016217128

7.. Takahashi T, Tamura M, Takasu T, Kamei S, Clinical and quantitative analysis of patients with crowned dens syndrome: J Neurol Sci, 2017; 376; 52-59

8.. Aouba A, Vuillemin-Bodaghi V, Mutschler C, De Bandt M, Crowned dens syndrome misdiagnosed as polymyalgia rheumatica, giant cell arteritis, meningitis or spondylitis: An analysis of eight cases: Rheumatology (Oxford), 2004; 43(12); 1508-12

9.. Zhang W, Doherty M, Pascual E, EULAR recommendations for calcium pyrophosphate deposition. Part II: management: Ann Rheum Dis, 2011; 70(4); 571-75

10.. Matsumura M, Hara S, Images in clinical medicine. Crowned dens syndrome: N Engl J Med, 2012; 367(23); e34

11.. Fakih O, Lohse A, A double crowned dens syndrome: Rheumatology (Oxford), 2023; 62(11); e331

12.. Francia A, Conte G, Platania G, An acute attack of calcium pyrophosphate deposition disease mimicking acute meningitis: Neurology, 2022; 99(10); 442-44

13.. Kohn NN, Hughes RE, Mccarty DJ, Faires JS, The significance of calcium phosphate crystals in the synovial fluid of arthritic patients: The “pseudogout syndrome”. II. Identification of crystals: Ann Intern Med, 1962; 56; 738-45

14.. Koyfman A, Yaffe D, Crowned dens syndrome. A case report: Neuroradiol J, 2014; 27(4); 495-97

15.. Abdelkefi I, Saidenberg-Kermanac’h N, Boissier MC, Crowned dens syndrome: Joint Bone Spine, 2022; 89(1); 105288

16.. Rammanohar J, Zhang C, Sidhu AA, An unusual case of neck pain: Crowned dens syndrome: Rheumatology (Oxford), 2021; 61(1); 471

17.. Naim T, Khan D, Ali M, Fanciullo J, Crowned dens syndrome: A challenging diagnosis in older adults presenting with acute neck pain: Cureus, 2023; 15(4); e37101

18.. Aichmair A, Herzog RJ, Perino G, Lebl DR, Recovery after cervical decompression surgery for the treatment of crowned dens syndrome causing progressive neurological decline: A case report: HSS J, 2014; 10(1); 83-87

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American Journal of Case Reports eISSN: 1941-5923
American Journal of Case Reports eISSN: 1941-5923