Perinpanathan Tanaraj, Beckett Katherine, Smith Chris
London North West University Healthcare NHS Trust, London, UK.
Clinical Research, Nagasaki University, Nagasaki, Japan.
Trop Med Health. 2024 Aug 26;52(1):55. doi: 10.1186/s41182-024-00610-7.
Actinomyces spp. are most commonly found in human commensal flora; however, they have also been shown to cause suppurative infections. We present a case of a rare Actinomyces funkei bacteraemia from an infected deep vein thrombosis in a patient who went on to develop pulmonary cavities secondary to septic emboli. Infected thrombi and septic emboli have been associated with other Actinomyces spp. in the literature, often posing a diagnostic challenge and, in some cases, causing drastic clinical deterioration in patients. The literature regarding Actinomyces funkei is scarce and to our knowledge there are no reports of a relationship between this Actinomyces subspecies and infected thrombi or septic emboli.
The patient was a 39-year-old known intravenous drug user who presented with a groin injecting site sinus and systemic symptoms. The bacteria was first observed by gram staining of a blood culture sample after 48 h of incubation and the species was identified using matrix-assisted laser desorption ionization time-of-flight (MALDI-TOF) as Actinomyces funkei. Sputum cytology/histology with cell block revealed a branching gram-positive species suspicious of slow growing bacteria or fungus. CT imaging of his lower limb and chest revealed an extensive DVT with inflammatory changes and pulmonary cavities respectively. The patient was treated with Ceftriaxone before being discharged with a 6-month course of Linezolid. He made a good recovery with reduction in size of the cavitating lung lesions on follow-up imaging.
This case report presents a difficult-to-diagnose bacterial infection in an intravenous drug user, complicated by bacteraemia and secondary septic emboli. Relatively little is known about Actinomyces funkei, and therefore this report aims to increase clinician awareness of diagnosis, management, and complications.
放线菌属最常见于人类共生菌群中;然而,它们也可引起化脓性感染。我们报告一例罕见的弗氏放线菌败血症病例,该患者因感染性深静脉血栓形成,继发脓毒性栓子导致肺空洞。在文献中,感染性血栓和脓毒性栓子与其他放线菌属有关,常常带来诊断挑战,在某些情况下,还会导致患者临床病情急剧恶化。关于弗氏放线菌的文献较少,据我们所知,尚无该放线菌亚种与感染性血栓或脓毒性栓子之间关系的报道。
患者为一名39岁的静脉注射吸毒者,出现腹股沟注射部位窦道及全身症状。血培养样本孵育48小时后,通过革兰氏染色首次观察到细菌,并使用基质辅助激光解吸电离飞行时间质谱(MALDI-TOF)鉴定为弗氏放线菌。痰细胞学/组织学检查及细胞块显示一种分支革兰氏阳性菌,怀疑为生长缓慢的细菌或真菌。其下肢和胸部的CT成像分别显示广泛的深静脉血栓形成伴炎症改变及肺空洞。患者在出院前接受了头孢曲松治疗,随后接受了为期6个月的利奈唑胺治疗。随访成像显示肺空洞病变缩小,患者恢复良好。
本病例报告了一名静脉注射吸毒者中难以诊断的细菌感染,并发败血症和继发性脓毒性栓子。关于弗氏放线菌的了解相对较少,因此本报告旨在提高临床医生对其诊断、管理和并发症的认识。