[A case of SAPHO syndrome with paraplegia due to a thoracic kyphosis].

Ryumachi. [Rheumatism] Pub Date : 2002-08-01
Tomoko Fujii, Koh Matsudaira, Hiromi Oda, Atsushi Seichi, Kozo Nakamura
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Abstract

A 63-year-old man visited our hospital in January 1993 because of back pain, which had been present for a year and persisted. The patient was diagnosed compression fracture of thoracic spine by another hospital. Thoracic plain radiographs revealed destructive and sclerotic changes with reduction of height of T 8, T 9 vertebral body. He had kyphosis on this level. Radiographs of the chest revealed hyperostosis of bilateral proximal clavicle. We diagnosed SAPHO syndrome (synovitis, acne, pustlosis, hyperostosis, and osteomyelitis: SAPHO) with T 8, T 9 spondylodiscitis, however without any skin manifestations. Oral indomethacin was effective, however thoracic kyphosis progressed gradually. Spastic gait and paraplegia appeared from February 1998, at last on July he was unable to walk independently. MRI showed the compression of spinal cord on T 8, T 9 level. We performed circumferential decompression and fusion with instrumentation. His paraplegia improved after surgery. We describe a rare case of SAPHO syndrome with paraplegia due to a thoracic kyphosis.

[SAPHO综合征并发胸后凸性截瘫1例]。
一名63岁男子于1993年1月因背痛来我院就诊,背痛已持续一年。外院诊断为胸椎压缩性骨折。胸部x线平片显示t8、t9椎体高度降低,破坏和硬化改变。他在这个部位有后凸。胸部x线片显示双侧锁骨近端骨质增生。我们诊断SAPHO综合征(滑膜炎、痤疮、脓疱病、骨质增生和骨髓炎:SAPHO)伴t8、t9脊椎炎,但无任何皮肤表现。口服吲哚美辛有效,但胸后凸逐渐加重。从1998年2月开始出现步态痉挛和截瘫,最终在7月无法独立行走。MRI显示脊髓在t8、t9水平受压。我们进行了周向减压和内固定融合。手术后他的截瘫有所改善。我们描述了一个罕见的SAPHO综合征与截瘫由于胸后凸。
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