Soma Tomoya, Asoda Seiji, Kimura Moemi, Munakata Kanako, Miyashita Hidetaka, Nakagawa Taneaki, Kawana Hiromasa
Division of Oral and Maxillofacial Surgery, Department of Dentistry and Oral Surgery, Keio University School of Medicine, 35 Shinanomachi, Shinjuku-ku, Tokyo, 160-8582, Japan.
J Med Case Rep. 2019 May 13;13(1):143. doi: 10.1186/s13256-019-2084-x.
Calcium pyrophosphate dihydrate crystal deposition disease is a condition in which calcium pyrophosphate dihydrate crystal is deposited in joint cartilage and ligaments. Calcium pyrophosphate dihydrate crystal deposition disease that involves calcification around the odontoid process of the second cervical vertebra is called crowned dens syndrome. Crowned dens syndrome is accompanied by fever in addition to acute and intense neck, posterior head, and temporal pain; thus, distinguishing crowned dens syndrome may be difficult in the presence of odontogenic infection. To the best of our knowledge, this is the first report describing a patient with crowned dens syndrome with coexisting odontogenic infection.
A 75-year-old Japanese woman was examined in the Emergency Department of this hospital due to a chief complaint of worsened buccal swelling on the left side. An odontogenic infection was considered, and she underwent her first examination. She presented with a body temperature of 37.4 °C, marked swelling and tenderness of her left lower eyelid through to her left cheek, and pain on the left temporal area. Blood tests revealed a leukocyte count of 6700/μL and a C-reactive protein level of 7.15 mg/dL. There was swelling and pain around the gingiva and acute purulent apical periodontitis of left maxillary second premolar. Cellulitis of the left cheek was diagnosed. After performing drainage of the pus, antibiotic treatment was initiated. Although her clinical symptoms improved, blood tests on day 9 of hospitalization revealed a leukocyte count of 6500/μL and a C-reactive protein level of 25.62 mg/dL, which were indicative of worsening symptoms. Computed tomography was performed to evaluate remote infection and images revealed a calcification around the odontoid process of her second cervical vertebra. When she was referred to the Orthopedic Surgery Department, pseudogout of the cervical spine was diagnosed. Subsequently, oral acetaminophen was initiated, and both her leukocyte count and C-reactive protein improved markedly.
In the presence of persistent fever and abnormally high leukocyte and C-reactive protein indicative of an inflammatory reaction, coexistence of pseudogout should be considered. In particular, when symptoms of temporal pain are present, the possibility of pseudogout of the cervical spine must be considered in the differential diagnosis.
二水焦磷酸钙晶体沉积病是一种二水焦磷酸钙晶体沉积于关节软骨和韧带的疾病。累及第二颈椎齿突周围钙化的二水焦磷酸钙晶体沉积病称为齿突冠综合征。齿突冠综合征除了伴有颈部、后头部和颞部急性剧烈疼痛外,还伴有发热;因此,在存在牙源性感染的情况下,鉴别齿突冠综合征可能会很困难。据我们所知,这是第一例描述患有齿突冠综合征并伴有牙源性感染的患者的报告。
一名75岁的日本女性因左侧颊部肿胀加重为主诉到本院急诊科就诊。考虑为牙源性感染,她接受了首次检查。她体温37.4°C,左侧下眼睑至左侧脸颊明显肿胀、压痛,左侧颞部疼痛。血液检查显示白细胞计数为6700/μL,C反应蛋白水平为7.15mg/dL。左侧上颌第二前磨牙牙龈周围肿胀、疼痛,伴有急性化脓性根尖周炎。诊断为左侧脸颊蜂窝织炎。在进行脓液引流后,开始抗生素治疗。尽管她的临床症状有所改善,但住院第9天的血液检查显示白细胞计数为6500/μL,C反应蛋白水平为25.62mg/dL,这表明症状在恶化。进行了计算机断层扫描以评估远处感染,图像显示她第二颈椎齿突周围有钙化。当她被转诊至骨科时,被诊断为颈椎假性痛风。随后,开始口服对乙酰氨基酚,她的白细胞计数和C反应蛋白均明显改善。
在存在持续发热以及提示炎症反应的白细胞和C反应蛋白异常升高的情况下,应考虑假性痛风的并存。特别是当出现颞部疼痛症状时,在鉴别诊断中必须考虑颈椎假性痛风的可能性。