耻骨联合结核性骨髓炎1例

Avinash Meda, Raju Kulkarni, Shivraj A C
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引用次数: 0

摘要

不到2%的血液性骨髓炎发生在耻骨联合,使其成为一种非常罕见的疾病。在所有肺外结核病例中,10-15%是由骨骼结核引起的。我们描述了一例罕见的由结核引起的耻骨骨髓炎,患者为一名58岁的女性,她最初主诉在耻骨上区出院8个月。病人因怀疑结核引起耻骨联合骨髓炎而入院。根据术前研究,计划手术。由于怀疑是肺结核,我们进行了清创,并插入了刺激抗生素珠。送CB-NAAT和组织病理学标本。当CB-NAAT对耐多药结核病(MDR-TB)检测呈阳性并开始抗结核治疗(ATT)时,HPR显示肉芽肿性炎症。在接受耐多药结核病治疗后,没有从该地点出院。手术后,有一年的随访。病人完全康复,无任何局部分泌物。这个例子说明了我们治疗结核引起的耻骨联合骨髓炎的方法。耻骨联合骨髓炎,刺激抗生素水泥珠,CB-NAAT,耐多药结核,ATT。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A rare case report of tuberculosis osteomyelitis of pubic symphysis
Less than 2% of all hematogenous osteomyelitis occurs in the pubic symphysis, making it a very uncommon condition. 10-15% of all instances of extra-pulmonary tuberculosis are caused by skeletal TB. We describe a rare instance of pubic osteomyelitis caused by tuberculosis in a 58-year-old woman who initially complained of discharge in the suprapubic region for 8 months. Patient was admitted due to suspected pubic symphysis osteomyelitis caused by TB. Based on preoperative studies, surgery was planned. Due to a suspicion of tuberculosis, debridement was performed and stimulan antibiotic beads were inserted. CB-NAAT and histopathology samples were sent. When CB-NAAT tested positive for multidrug-resistant tuberculosis (MDR-TB) and started on antitubercular therapy (ATT), HPR indicated granulomatous inflammation. After receiving MDR-TB treatment, there was no discharge from the location. Following surgery, there was a year of follow-up. Patient made a full recovery without any site discharge. This example serves to illustrate our approach to treating pubic symphysis osteomyelitis caused by TB. Osteomyelitis of the pubic symphysis, stimulating antibiotic cement beads, CB-NAAT, MDRTB, ATT.
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