Rolemberg Dantas Fernando Luiz, Dantas François, Tscherbakowski Nunes de Guimarães Mourão Rômulo, Campos Mattos Bárbara, Kelles Tupy da Fonseca Victor
Neurological Surgery, Biocor Instituto, Belo Horizonte, BRA.
Neurological Surgery, Faculdade Ciências Médicas de Minas Gerais, Belo Horizonte, BRA.
Cureus. 2024 Jul 20;16(7):e64974. doi: 10.7759/cureus.64974. eCollection 2024 Jul.
Synovitis, acne, pustulosis, hyperostosis, osteitis (SAPHO) syndrome is a rare disorder of unknown etiology with heterogeneous clinical manifestations. We describe two cases of patients diagnosed with SAPHO syndrome mimicking spinal bone metastases. A literature review was conducted to identify similar previously reported cases. The first patient was a 56-year-old woman with progressive back pain for six months who was referred to the neurosurgery department for suspected spinal metastases. A spinal CT scan revealed hyperdense lesions at T10 and hyperdense changes in the lumbar vertebrae. Spinal MRI demonstrated bone marrow edema that was hypointense on T1-weighted imaging and hyperintense on T2-weighted imaging in multiple thoracic vertebrae, and the PET/CT showed multiple skeletal lesions affecting the spine with low-to-moderate F-FDG uptake. Scintigraphy showed the characteristic "bull's head" sign with increased uptake in the manubrium and bilateral sternoclavicular joints. The second patient was a 66-year-old woman with a four-month history of back pain, who was admitted with multiple spinal lesions. The diagnosis was made after bone scintigraphy demonstrated the characteristic findings of the syndrome. Both patients lacked cutaneous lesions on presentation but reported previous skin lesions. SAPHO syndrome is a rare condition, and bone lesions associated with the disease may be misdiagnosed as bone metastases. Knowledge of the syndrome and its imaging findings is essential for accurate diagnosis and treatment.
滑膜炎、痤疮、脓疱病、骨肥厚、骨炎(SAPHO)综合征是一种病因不明的罕见疾病,临床表现多样。我们描述了两例被诊断为酷似脊柱骨转移瘤的SAPHO综合征患者。进行了文献综述以确定先前报道的类似病例。首例患者为一名56岁女性,有6个月的进行性背痛,因疑似脊柱转移瘤被转诊至神经外科。脊柱CT扫描显示T10椎体高密度病变及腰椎高密度改变。脊柱MRI显示多个胸椎骨髓水肿,T1加权像呈低信号,T2加权像呈高信号,PET/CT显示多个累及脊柱的骨骼病变,F-FDG摄取呈低至中度。骨闪烁显像显示特征性的“牛头”征,胸骨柄及双侧胸锁关节摄取增加。第二例患者为一名66岁女性,有4个月的背痛病史,因多发脊柱病变入院。骨闪烁显像显示该综合征的特征性表现后确诊。两名患者初诊时均无皮肤病变,但均报告既往有皮肤病变。SAPHO综合征是一种罕见疾病,与该疾病相关的骨病变可能被误诊为骨转移瘤。了解该综合征及其影像学表现对于准确诊断和治疗至关重要。