Tabetic Arthropathy: A Historical Multiple Localization

H. Arabi, Hafida Bara, A. Mougui, I. E. Bouchti
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Abstract

Tabetic arthropathy is a rare complication of neurosyphilis. It has currently become rare due to the decreased frequency of syphilis and early treatment. We report a case of tabetic arthropathy with multiple localizations. The patient is a 67-year-old individual with no particular medical history. He was hospitalized for painless deformities of both knees and the right elbow, which had been progressing for 25 years, accompanied by the sudden onset of swelling in the left knee, progressing with remission. Later, he developed similar swelling in the right knee and elbow. Subsequently, he experienced progressive and painless instability in both knees, resulting in total functional disability. Standard X-rays of the right elbow, both knees, and the left hand revealed significant joint destruction. Given the discrepancy between the extent of radiological destruction and the painlessness of the affected joint arthropathy, the diagnosis of neurogenic arthropathy was considered. Serology for syphilis was positive (TPHA + and VDRL -) in both blood and cerebrospinal fluid. The diagnosis of polyarticular tabetic arthropathy was confirmed. The patient was treated with a third-generation cephalosporin at a dose of 2g per day intravenously for 21 days. This is a rare case of late-diagnosed multifocal tabetic arthropathy with a catastrophic outcome.
塔贝特关节病历史上的多重定位
Tabetic关节病是神经梅毒的一种罕见并发症。由于梅毒发病率的降低和早期治疗,这种病目前已变得非常罕见。我们报告了一例多发的表皮关节病。患者现年67岁,无特殊病史。他因双膝关节和右肘无痛性畸形住院,这种畸形已持续了 25 年,伴有突然出现的左膝关节肿胀,肿胀逐渐缓解。后来,他的右膝和右肘也出现了类似的肿胀。随后,他的双膝逐渐出现无痛性不稳,导致完全丧失功能。右肘、双膝和左手的标准 X 光片显示关节严重受损。鉴于放射学破坏程度与受影响关节的无痛性之间存在差异,考虑诊断为神经源性关节病。血液和脑脊液中的梅毒血清学检查均呈阳性(TPHA + 和 VDRL -)。多关节表型关节病的诊断得到确认。患者接受了第三代头孢菌素治疗,每天静脉注射 2 克,持续 21 天。这是一例罕见的晚期诊断的多灶性扁桃体关节病,并造成了灾难性的后果。
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