Department of Infectious Diseases, Japanese Red Cross Ise Hospital, Mie, Japan.
Infection Prevention and Control Office, Japanese Red Cross Ise Hospital, Mie, Japan.
Medicine (Baltimore). 2023 Aug 25;102(34):e34968. doi: 10.1097/MD.0000000000034968.
Clinically, vertebral osteomyelitis commonly occurs in immunocompromised individuals, such as people with diabetes, immunosuppression, chronic liver disease, and malignancy. Microbiologically, vertebral osteomyelitis is commonly caused by Staphylococcus aureus; however, Streptococcus dysgalactiae subspecies equisimilis (SDSE) may also potentially cause vertebral osteomyelitis, albeit rarely. Since no case reports have documented the occurrence of SDSE cervical osteomyelitis accompanied by progressive atlantoaxial subluxation, its clinical characteristics remain uncertain. Herein, we report the first case of progressive atlantoaxial subluxation in addition to cervical osteomyelitis due to septic atlantoaxial arthritis caused by SDSE in an immunocompetent individual, and provide a review of the relevant literature.
A 63-year-old man with hypertension but no history of trauma or musculoskeletal disorders presented with worsening neck pain for 1 month without fever. Physical examination revealed neck pain due to neck retroflexion and tenderness with swelling of the upper cervical spine. No neurological deficit was observed. Magnetic resonance imaging revealed low-intensity areas on a T1-weighted image and high-intensity areas on a short tau inversion recovery image at the C2, C5, and C6 vertebral bodies with atlantoaxial subluxation. Two sets of blood culture tests (aerobic and anaerobic) were performed.
The anaerobic blood culture bottle showed the presence of beta-hemolytic pyrrolidonyl arylamidase-negative SDSE expressing Lancefield group A antiserum. Hence, the patient was diagnosed with SDSE cervical osteomyelitis with atlantoaxial subluxation; intensive intravenous ampicillin (2 g every 6 hours) - which is effective against SDSE - was administered.
Posterior fusion (occipital bone, C4) was performed on day 33 because a follow-up magnetic resonance imaging on day 31 revealed progression of atlantoaxial subluxation with thickened atlantodental soft tissue.
The patient's neck pain was completely relieved after treatment with intravenous ampicillin for 6 weeks, followed by oral amoxicillin (1500 mg) daily for an additional 4 weeks. The patient did not experience recurrence or sequelae during the 2-year follow-up period.
SDSE expressing Lancefield group A antiserum can cause afebrile vertebral osteomyelitis and progressive atlantoaxial subluxation due to the occurrence of septic atlantoaxial arthritis in immunocompetent individuals. Spinal instrumentation for vertebral osteomyelitis may be acceptable after 6 weeks of antimicrobial therapy.
临床上,椎体骨髓炎常发生于免疫功能低下的个体,如糖尿病、免疫抑制、慢性肝病和恶性肿瘤患者。微生物学上,椎体骨髓炎常由金黄色葡萄球菌引起;然而,似无乳链球菌马亚种(SDSE)也可能潜在地导致椎体骨髓炎,尽管很少见。由于尚无病例报告记录 SDSE 引起的颈椎骨髓炎伴有进行性寰枢关节半脱位,其临床特征尚不确定。在此,我们报告首例免疫功能正常个体由 SDSE 引起的化脓性寰枢关节炎导致的进行性寰枢关节半脱位伴颈椎骨髓炎,并对相关文献进行回顾。
一名 63 岁男性,有高血压但无外伤或肌肉骨骼疾病史,因颈痛加重 1 个月(无发热)就诊。体格检查发现颈椎后伸时颈痛和上颈椎压痛伴肿胀。无神经功能缺损。磁共振成像显示 C2、C5 和 C6 椎体 T1 加权图像低信号和短 tau 反转恢复图像高信号,伴有寰枢关节半脱位。进行了两组血培养(需氧和厌氧)。
厌氧血培养瓶显示存在β-溶血吡咯烷酮芳基酰胺阴性 SDSE,表达兰斯菲尔德组 A 抗血清。因此,患者诊断为 SDSE 致颈椎骨髓炎伴寰枢关节半脱位;给予静脉注射氨苄西林(2 g 每 6 小时)——对 SDSE 有效。
第 33 天因第 31 天的随访磁共振成像显示寰枢关节半脱位进展伴齿状突软组织结构增厚而行后路寰枢融合(枕骨、C4)。
静脉注射氨苄西林 6 周后,患者的颈痛完全缓解,随后口服阿莫西林(1500 mg)每日 1 次,共 4 周。在 2 年的随访期间,患者未出现复发或后遗症。
表达兰斯菲尔德组 A 抗血清的 SDSE 可引起无热的脊椎骨髓炎和进行性寰枢关节半脱位,原因是免疫功能正常个体发生化脓性寰枢关节炎。抗菌治疗 6 周后,脊椎器械治疗脊椎骨髓炎可能是可以接受的。