Nouri Mohammad, Alsaif Malak, Alnufaei Abdulaziz, Alhassan Turki
Division of Plastic Surgery, Department of Surgery, King Abdulaziz Medical City, Ministry of National Guard Health Affairs (MNGHA), Riyadh, Saudi Arabia.
King Abdullah International Medical Research Center (KAIMRC), Riyadh, Saudi Arabia.
Case Reports Plast Surg Hand Surg. 2025 Aug 9;12(1):2545199. doi: 10.1080/23320885.2025.2545199. eCollection 2025.
Although less commonly in the hand, gouty tenosynovitis may present with symptoms resembling infection. Only a few case reports document such presentations, and reports of coexisting infection and gouty tenosynovitis are even more uncommon. A 32-year-old male with polyarticular tophaceous gout, noncompliant with medications, presented with a one-day history of right index finger swelling and redness. Investigations were suggestive of infectiousious tophus. Despite broad-spectrum antibiotics and rheumatologic interventions (colchicine, allopurinol, and corticosteroids), his condition deteriorated. Multiple incisions and drainages were performed without improvement. Persistent infection, confirmed to be methicillin-resistant Staphylococcus aureus (MRSA), complicated the underlying gouty inflammation. Standard therapies for infective tenosynovitis did not yield clinical resolution, presumably due to ongoing crystal-induced inflammation and compromised tissue. Ultimately, finger amputation was performed to control disease progression after all other salvage options failed. This case underscores the aggressive and destructive potential of gout when complicated by infection. Normal or relatively low serum uric acid levels do not exclude gout, and synovial fluid crystal analysis can be pivotal. Coexisting infection and gouty tenosynovitis in the hand can lead to severe tissue damage if misdiagnosed or inadequately treated. A high index of suspicion, multidisciplinary collaboration, and timely surgical intervention are crucial in preventing further morbidity. This case demonstrates that amputation may be necessary when infection remains unresponsive to standard treatments, emphasizing the importance of early diagnosis and aggressive management.
虽然痛风性腱鞘炎在手部较少见,但可能表现出类似感染的症状。仅有少数病例报告记录了此类表现,而关于合并感染和痛风性腱鞘炎的报告更为罕见。一名32岁患有多关节痛风石性痛风且不遵医嘱服药的男性,出现右手示指肿胀和发红1天的症状。检查提示感染性痛风石。尽管使用了广谱抗生素和风湿科干预措施(秋水仙碱、别嘌醇和皮质类固醇),但其病情仍恶化。多次切开引流均无改善。确诊为耐甲氧西林金黄色葡萄球菌(MRSA)的持续性感染,使潜在的痛风性炎症复杂化。感染性腱鞘炎的标准治疗未取得临床缓解,可能是由于持续的晶体诱导炎症和组织受损。最终,在所有其他挽救措施均失败后,为控制疾病进展进行了手指截肢。该病例强调了痛风合并感染时的侵袭性和破坏性潜力。血清尿酸水平正常或相对较低并不能排除痛风,滑膜液晶体分析可能至关重要。手部合并感染和痛风性腱鞘炎如果误诊或治疗不当,可导致严重的组织损伤。高度的怀疑指数、多学科协作以及及时手术干预对于预防进一步的发病至关重要。该病例表明,当感染对标准治疗无反应时,截肢可能是必要的,强调了早期诊断和积极治疗的重要性。