SAPHO综合征模拟感染性脊椎炎和骨转移。

Case Reports in Rheumatology Pub Date : 2021-09-04 eCollection Date: 2021-01-01 DOI:10.1155/2021/5577257
S Biuden, K Maatallah, H Riahi, H Ferjani, M D Kaffel, W Hamdi
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引用次数: 2

摘要

缩写SAPHO(滑膜炎、痤疮、脓疱病、骨质增生和骨炎)包括具有类似骨关节表现和皮肤状况的疾病。做出这种诊断并不总是显而易见的,特别是当临床表现不符合疾病的典型模式或发生在特定领域时。我们描述了三个诊断困难的病例。一名46岁女性,以颈椎疼痛为主诉。颈椎x线片显示象牙状C5椎体。然而,患者的一般情况保持良好,没有潜在的肿瘤迹象,也没有其他关节不适。血液分析正常。断层扫描未发现任何可疑病变,但显示柄部硬化和骨质增生。闪烁成像显示典型的“牛头”状。一名61岁女性患有胸腰椎疼痛。MRI示D3-D4、D4-D5、D5-D6、D6-D7、L1-L2椎间盘炎伴椎旁软组织受累,模拟感染性椎间盘炎。两次感染性检查和发现性活检均为阴性。随后怀疑SAPHO综合征。骨显像显示软骨胸骨关节和D4至D7椎体摄取。建立SAPHO的诊断。第三例患者为46岁男性,患有肺腺癌。转移性疾病分期,进行TAP断层扫描,显示D8至D12骨硬化和骶髂关节关节内桥。MRI和显像排除恶性肿瘤,确认SAPHO的诊断。在我们的病例中,影像学表现可以帮助鉴别SAPHO综合征与其他疾病。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

SAPHO Syndrome Mimicking Infectious Spondylodiscitis and Bone Metastasis.

SAPHO Syndrome Mimicking Infectious Spondylodiscitis and Bone Metastasis.

SAPHO Syndrome Mimicking Infectious Spondylodiscitis and Bone Metastasis.

SAPHO Syndrome Mimicking Infectious Spondylodiscitis and Bone Metastasis.

The acronym SAPHO (synovitis, acne, pustulosis, hyperostosis, and osteitis) includes diseases with similar osteoarticular manifestations and skin conditions. Making this diagnosis is not always obvious, especially when the clinical presentation does not fit the typical pattern of the disease or it occurs in a particular field. We described three cases where the diagnosis was difficult. A 46 year-old woman presented with cervical pain. The cervical X-ray showed the aspect of an ivory C5 vertebra. The patient had, however, preserved general condition, no signs of underlying neoplasia, nor other joint complaints. Blood analysis was normal. Tomography did not find any suspect lesion but showed sclerosis and hyperostosis of the manubrium. Scintigraphy showed the characteristic "bullhead" appearance. A 61-year-old woman had thoracic and lumbar pain. MRI showed spondylodiscitis in D3-D4, D4-D5, D5-D6, D6-D7, and L1-L2 with paraspinal soft tissue involvement, simulating infectious spondylodiscitis. Infectious investigations and discovertebral biopsy performed twice were negative. SAPHO syndrome was then suspected. Bone scintigraphy showed uptake in the chondrosternal articulations and D4 to D7 vertebrae. The diagnosis of SAPHO was established. The third case was a 46-year-old man with a lung adenocarcinoma. Staging for metastatic disease, a TAP tomography was performed and showed osteosclerosis of D8 to D12 and intra-articular bridges in the sacroiliac joints. MRI and scintigraphy eliminated malignancy and confirmed the diagnosis of SAPHO. In our cases, imaging findings could facilitate differentiating SAPHO syndrome from other diseases.

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