Rare Causes of Musculoskeletal Pain: Thinking beyond Common Rheumatologic Diseases.

Case Reports in Rheumatology Pub Date : 2024-01-18 eCollection Date: 2024-01-01 DOI:10.1155/2024/6540026
Julia F Charles, Alan O Malabanan, Stan Krolczyk, Kathryn M Dahir
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引用次数: 0

Abstract

Objectives: Rare metabolic bone diseases can present with symptoms mimicking more common rheumatological conditions including spondyloarthritis, osteoarthritis, and fibromyalgia. Increasing awareness of these rare diseases within the rheumatology community is vital to ensure that affected patients are diagnosed and appropriately treated. The literature includes several reports of tumour-induced osteomalacia initially diagnosed as rheumatic disease, but other rare diseases such as X-linked hypophosphatemia (XLH) and hypophosphatasia (HPP) also deserve attention. Here, we describe two cases of adult patients incorrectly diagnosed with ankylosing spondylitis and osteoarthritis who, upon referral to a metabolic bone disease specialist, were subsequently diagnosed with XLH and HPP, respectively, profoundly altering their management.

Methods: The cases were collected from Brigham and Women's Hospital, Boston, MA, USA, and Vanderbilt University Medical Center, Nashville, TN, USA.

Results: Details of the patients' respective medical and family histories are presented, and the clinical and biochemical investigations undertaken to reach the correct diagnoses are described.

Conclusion: Rheumatologists should be encouraged to think beyond common rheumatological diseases when faced with symptoms such as bone pain, muscle pain, and stiffness, especially when accompanied by manifestations including atraumatic fractures, poor dentition, and hearing loss. In cases where one of these rare diseases is suspected, referral to a metabolic bone disease specialist for confirmation of diagnosis is encouraged as effective treatment options have recently become available.

肌肉骨骼疼痛的罕见病因:超越常见风湿病的思考。
目的:罕见代谢性骨病的症状可能与脊柱关节炎、骨关节炎和纤维肌痛等更常见的风湿病相似。提高风湿病学界对这些罕见疾病的认识对于确保受影响的患者得到诊断和适当治疗至关重要。文献中有多篇关于肿瘤诱发的骨软化症最初被诊断为风湿病的报道,但其他罕见疾病如X连锁低磷血症(XLH)和低磷血症(HPP)也值得关注。在此,我们描述了两例被误诊为强直性脊柱炎和骨关节炎的成年患者,他们在转诊至代谢性骨病专科医生后,分别被诊断为 XLH 和 HPP,这深刻地改变了他们的治疗方法:这些病例来自美国马萨诸塞州波士顿布里格姆妇女医院和美国田纳西州纳什维尔范德比尔特大学医学中心:结果:详细介绍了患者各自的病史和家族史,并描述了为得出正确诊断而进行的临床和生化检查:结论:应鼓励风湿病学家在面对骨痛、肌肉痛和僵硬等症状,尤其是伴有非创伤性骨折、牙齿不齐和听力下降等表现时,不要局限于常见的风湿病。如果怀疑是这些罕见疾病中的一种,应转诊至代谢性骨病专科医生进行确诊,因为最近已经出现了有效的治疗方案。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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