足部骨髓水肿综合征误诊为感染1例

Lauren Shute , Elly Trepman , Derek Bueddefeld , Gerhard Bock , John M. Embil
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摘要

骨髓水肿综合征是一种罕见的,自限性的临床实体,病因不明,可能被误诊为感染。一名62岁男子出现左脚疼痛,之前没有外伤。两周内,由于疼痛加剧,他无法行走。5周时,患者出现左脚肿胀。x线片显示足中部骨质减少。他被推测为痛风和感染,用非甾体抗炎药、万古霉素和头孢曲松治疗,但没有改善。磁共振显示骨髓水肿,脑皮层模糊。单光子发射计算机断层扫描、计算机断层扫描和骨显像显示左足中部强烈的骨摄取、斑片状脱矿和侵蚀改变。骨髓水肿综合征的诊断是基于对影像学表现的回顾和既往治疗后的持续症状。经镇痛药和卸骨装置治疗后,患者疼痛完全缓解,症状出现5个月后足中骨质减少得到改善。总之,足部骨髓水肿综合征是罕见的,对这种综合征的认识是必要的,以避免诊断错误和不必要的治疗。如果磁共振成像是不可用的,单光子发射计算机断层扫描-计算机断层扫描可能是一个有用的辅助诊断。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Bone marrow edema syndrome of the foot misdiagnosed as infection: Case report
Bone marrow edema syndrome is a rare, self-limited clinical entity of unknown etiology and may be misdiagnosed as an infection. A 62-year-old man developed left foot pain with no prior trauma. Within 2 weeks, he was unable to walk because of increased pain. At 5 weeks, he developed left foot swelling. Radiographs showed midfoot osteopenia. He was treated for presumed gout and infection with nonsteroidal anti-inflammatory drugs, vancomycin, and ceftriaxone but had no improvement. Magnetic resonance imaging showed bone marrow edema and indistinct cortices. Single-photon emission computed tomography–computed tomography and bone scintigraphy showed intense osseous uptake, patchy demineralization, and erosive changes at the left midfoot. The diagnosis of bone marrow edema syndrome was made, based on review of imaging findings and persistent symptoms despite previous treatment. After treatment with analgesics and off-loading devices, he had complete resolution of pain and improvement of midfoot osteopenia by 5 months after symptom onset. In summary, bone marrow edema syndrome in the foot is rare, and awareness of this syndrome is necessary to avoid diagnostic error and unnecessary treatment. If magnetic resonance imaging is not available, single-photon emission computed tomography–computed tomography may be a useful adjunct toward the diagnosis.
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