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一例罕见的以无菌性积液为表现的自发性肘部骨髓炎病例。

A Rare Case of Spontaneous Elbow Osteomyelitis Presenting With Aseptic Effusion.

作者信息

Rodriguez Aquino Eddie G, Agrait Gonzalez Miguel F, Marrero Medina Sarah, Laracuente Israel

机构信息

Emergency Medicine, Centro Medico Episcopal San Lucas, Ponce, PRI.

出版信息

Cureus. 2025 Mar 9;17(3):e80305. doi: 10.7759/cureus.80305. eCollection 2025 Mar.

Abstract

Spontaneous osteomyelitis of the capitellum is an exceptionally rare condition, particularly in the absence of identifiable risk factors or inciting events. This case report describes a previously healthy 20-year-old male who presented with progressive elbow pain and swelling, initially raising suspicion for septic arthritis. Point-of-care ultrasound (POCUS) identified a significant joint effusion, and subsequent arthrocentesis revealed purulent fluid with a high white blood cell count, strongly suggestive of a septic joint. The patient was treated empirically with antibiotics and underwent surgical debridement, but cultures from both the arthrocentesis and the surgical washout were negative. Further imaging with MRI ultimately revealed findings consistent with osteomyelitis of the capitellum. This case highlights the diagnostic challenges associated with musculoskeletal infections, particularly in atypical sites like the capitellum, and underscores the importance of advanced imaging modalities such as MRI when initial diagnostics are inconclusive. The report also emphasizes the utility of POCUS in identifying joint effusions and guiding arthrocentesis in the emergency setting. Early recognition and appropriate management of osteomyelitis are crucial to avoid serious complications such as chronic infection, joint dysfunction, or limb deformity. This case contributes to the limited literature on capitellum osteomyelitis, particularly in the setting of an aseptic effusion, and advocates for the integration of multidisciplinary approaches and advanced diagnostic tools in the evaluation of pediatric and young adult musculoskeletal infections. Further research is needed to better understand the pathophysiology and management of rare presentations like this one.

摘要

肱骨小头自发性骨髓炎是一种极为罕见的病症,尤其是在没有可识别的风险因素或诱发事件的情况下。本病例报告描述了一名此前健康的20岁男性,他出现了进行性肘部疼痛和肿胀,最初怀疑是化脓性关节炎。床旁超声(POCUS)发现有大量关节积液,随后的关节穿刺抽出了白细胞计数很高的脓性液体,强烈提示为化脓性关节。该患者接受了经验性抗生素治疗并接受了手术清创,但关节穿刺和手术冲洗的培养结果均为阴性。进一步的MRI检查最终显示出与肱骨小头骨髓炎相符的结果。本病例突出了与肌肉骨骼感染相关的诊断挑战,尤其是在像肱骨小头这样的非典型部位,并强调了在初始诊断不确定时MRI等先进成像方式的重要性。该报告还强调了POCUS在急诊环境中识别关节积液和指导关节穿刺方面的实用性。骨髓炎的早期识别和适当管理对于避免诸如慢性感染、关节功能障碍或肢体畸形等严重并发症至关重要。本病例为关于肱骨小头骨髓炎的有限文献做出了贡献,特别是在无菌性积液的情况下,并提倡在评估儿童和青年肌肉骨骼感染时采用多学科方法和先进诊断工具。需要进一步研究以更好地理解此类罕见表现的病理生理学和管理方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d6a8/11977443/e3ead56fd6eb/cureus-0017-00000080305-i01.jpg

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