Sidhu Alamjeet K, Khandelwal Shreya, Dominic Savio Francis V, Bedi Simranjeet, Pathak Yashash D
Kharkiv National Medical University, Ukraine.
B.P. Koirala Institute of Health Sciences, Nepal.
Ann Med Surg (Lond). 2024 Aug 30;86(10):6246-6250. doi: 10.1097/MS9.0000000000002515. eCollection 2024 Oct.
Tsukamurella species are rare, aerobic, gram-positive bacteria known to cause infections, primarily in immunocompromised individuals. This case report presents a rare instance of a mucosal infection caused by Tsukamurella species following a nasal septum procedure in an immunocompetent patient.
A 51-year-old man with a history of multiple hereditary exostosis, allergic rhinitis, and recent nasal fracture repair presented with persistent fevers and low back pain. Postoperatively, he developed sinus pain and small oral lesions, initially treated with antibiotics for presumed sinusitis. Despite treatment, his fever persisted, leading to an emergency department visit. Laboratory tests indicated sepsis, but a CT scan of the sinuses showed no sinusitis. Despite broad-spectrum antibiotics, the patient's fever continued. On admission day 9, nasal endoscopy and culture identified Tsukamurella species. The patient was treated with augmentin, fluconazole, and levofloxacin, leading to the resolution of symptoms and discharge with ongoing treatment.
Tsukamurella species are uncommon pathogens that are often associated with bacteremia in immunocompromised individuals. This case highlights the diagnostic challenges and the importance of considering unusual pathogens in postprocedural infections, even in immunocompetent patients. Accurate identification and appropriate management are critical in improving outcomes for patients with Tsukamurella infections.
This case underscores the need for vigilance in diagnosing rare infections like Tsukamurella, even in immunocompetent individuals. The successful resolution with combination therapy highlights the importance of appropriate antibiotic selection in managing such infections.
冢村菌属是罕见的需氧革兰氏阳性菌,已知可引发感染,主要发生在免疫功能低下的个体中。本病例报告呈现了一例在免疫功能正常的患者进行鼻中隔手术后由冢村菌属引起的罕见黏膜感染病例。
一名51岁男性,有多发遗传性外生骨疣、过敏性鼻炎病史,近期接受了鼻骨骨折修复手术,出现持续发热和腰痛。术后,他出现鼻窦疼痛和口腔小溃疡,最初因疑似鼻窦炎接受抗生素治疗。尽管进行了治疗,他的发热仍持续,遂前往急诊科就诊。实验室检查显示存在败血症,但鼻窦CT扫描未显示鼻窦炎。尽管使用了广谱抗生素,患者的发热仍持续。在入院第9天,鼻内镜检查和培养鉴定出冢村菌属。患者接受了阿莫西林克拉维酸钾、氟康唑和左氧氟沙星治疗,症状得以缓解并出院,仍在继续接受治疗。
冢村菌属是不常见的病原体,通常与免疫功能低下个体的菌血症有关。本病例突出了诊断挑战以及在术后感染中考虑不寻常病原体的重要性,即使是在免疫功能正常的患者中。准确识别和适当管理对于改善冢村菌属感染患者的预后至关重要。
本病例强调了即使在免疫功能正常的个体中,对于诊断像冢村菌属这样的罕见感染也需要保持警惕。联合治疗的成功缓解突出了在管理此类感染中选择合适抗生素的重要性。