系统性硬化症表现为手指骨髓炎:医生在评估有指尖溃疡或感染的患者时,必须保持对系统性硬化症的高度怀疑。

Logan Van Poucke, Jared B Hinton, Holly C Heck, Benjamin E Heck, Bruce E Heck
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引用次数: 0

摘要

导读:骨髓炎是一种严重的骨感染,通常由细菌性病原体引起,以金黄色葡萄球菌最为常见。这种情况对患有自身免疫性疾病(如硬皮病和雷诺综合征)的患者提出了重大挑战,血管功能障碍和免疫抑制增加了感染风险。本病例报告说明了这些条件之间复杂的相互作用,并强调了早期诊断和综合管理的重要性,以防止严重的并发症。病例报告:我们提出的情况下,79岁的女性雷诺综合征的历史和怀疑硬皮病谁发展骨髓炎的左中指支气管感染后。尽管进行了多次清创手术,患者仍经历了持续的疼痛和肿胀。体格检查显示受累手指出现坏死和坏疽,磁共振成像证实骨髓炎。培养鉴定出荣誉棒状杆菌,这是一种不常见的病原体。患者接受手术清创,随后进行抗生素治疗和血管扩张剂治疗。患者病情好转,随访时无感染迹象。结论:本病例强调了对自身免疫性疾病(如硬皮病和雷诺综合征)患者早期和彻底评估感染的迫切需要。这些疾病固有的血管功能障碍会加剧感染,导致骨髓炎等严重后果。涉及早期手术干预和量身定制的医疗管理的多学科方法对优化患者的结果至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Systemic Sclerosis Presenting as Osteomyelitis of the Finger: Physicians Must Maintain a High Index of Suspicion for Systemic Sclerosis when Evaluating Patients with Fingertip Ulceration or Infection.

Introduction: Osteomyelitis is a serious bone infection commonly caused by bacterial pathogens, with Staphylococcus aureus being the most prevalent. The condition poses significant challenges in patients with underlying autoimmune disorders such as scleroderma and Raynaud's syndrome, where vascular dysfunction and immunosuppression heighten infection risks. This case report illustrates the complex interplay between these conditions and underscores the importance of early diagnosis and comprehensive management to prevent severe complications.

Case report: We present the case of a 79-year-old female with a history of Raynaud's syndrome and suspected scleroderma who developed osteomyelitis of the left middle finger following a paronychial infection. The patient experienced persistent pain and swelling despite multiple debridement procedures. Physical examination revealed necrosis and gangrene of the affected finger, and magnetic resonance imaging confirmed osteomyelitis. Cultures identified Corynebacterium accolens, an uncommon pathogen in this context. The patient underwent surgical debridement, followed by antibiotic therapy and vasodilators. Her condition improved, with no signs of infection at follow-up.

Conclusion: This case highlights the critical need for early and thorough assessment of infections in patients with autoimmune conditions such as scleroderma and Raynaud's syndrome. The vascular dysfunction inherent in these diseases can exacerbate infections, leading to severe outcomes such as osteomyelitis. A multidisciplinary approach involving early surgical intervention and tailored medical management is essential to optimize patient outcomes.

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