Gupta Nitin, Banerjee Sayantan, Sharma Rohini, Roy Shambo Guha, Shende Trupti M, Ansari Mohammed Tahir, Singh Gagandeep, Nischal Neeraj, Wig Naveet, Soneja Manish
Infectious Disease Division, Departments of Medicine and Microbiology, All India Institute of Medical Sciences, New Delhi, India.
Department of Medicine, All India Institute of Medical Sciences, New Delhi, India.
Intractable Rare Dis Res. 2017 Aug;6(3):206-210. doi: 10.5582/irdr.2017.01029.
A 26-year-old male patient presented with features suggestive of osteomyelitis involving the entire left femur, hip joint and knee joint. Culture from the debrided tissue grew and he was treated with sensitivity based antibiotics but the symptoms did not resolve. The synovial biopsy showed multinucleated giant cells and acid fast bacilli on Ziehl Neelsen stain. Cartridge based nucleic acid amplification test (GeneXpert) was negative. The Mycobacteria growth indicator tube culture was found to be positive for . The patient was started on imipenem, amikacin and macrolide based therapy. There was partial response initially but the patient worsened again. A girdle stone arthroplasty with cemented nail (with tobramycin) insertion after debridement of the infected tissue was done. Potassium hydroxide (KOH) mount from the debridement sample was found to be positive for aseptate hyphae suggestive of mucormycosis. He was treated with liposomal amphotericin B. He was evaluated for immunodeficiency in view of multiple atypical infections and was found to have a low CD4 count. The patient was discharged on amikacin, azithromycin, trimethoprim-sulfamethoxazole and posaconazole. Follow up showed considerable resolution both clinically and radiologically. To our knowledge, this is the first reported case of osteomyelitis with co-infection of and mucormycetes. We report this case to highlight the possibility of multiple rare infections in patients with immunodeficiency. Also, atypical complicated bone infections, such as and mucormycetes might require combined medical and surgical treatment.
一名26岁男性患者表现出提示骨髓炎的特征,累及整个左股骨、髋关节和膝关节。清创组织培养生长出[具体病菌未提及],他接受了基于药敏的抗生素治疗,但症状未缓解。滑膜活检在齐-尼氏染色上显示有多核巨细胞和抗酸杆菌。基于 cartridge 的核酸扩增试验(GeneXpert)为阴性。分枝杆菌生长指示管培养发现[具体病菌未提及]呈阳性。患者开始接受基于亚胺培南、阿米卡星和大环内酯类的治疗。最初有部分反应,但患者病情再次恶化。在对感染组织进行清创后,进行了带骨水泥钉(含妥布霉素)植入的环行截骨成形术。清创样本的氢氧化钾(KOH)涂片发现有提示毛霉病的无隔菌丝呈阳性。他接受了脂质体两性霉素B治疗。鉴于多种非典型感染,对他进行了免疫缺陷评估,发现其 CD4 计数较低。患者出院时带药阿米卡星、阿奇霉素、复方新诺明和泊沙康唑。随访显示临床和影像学上均有明显好转。据我们所知,这是首例报告的骨髓炎合并[具体病菌未提及]和毛霉菌共感染的病例。我们报告此病例以强调免疫缺陷患者发生多种罕见感染的可能性。此外,非典型复杂性骨感染,如[具体病菌未提及]和毛霉菌可能需要联合药物和手术治疗。