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园艺活动后免疫功能正常患者的肌脓肿

Pyomyositis in an Immunocompetent Patient Following Gardening Activity.

机构信息

Jackson Memorial Hospital, Miami, FL, USA.

University of Miami, Miami, FL, USA.

出版信息

J Investig Med High Impact Case Rep. 2024 Jan-Dec;12:23247096241261508. doi: 10.1177/23247096241261508.

DOI:10.1177/23247096241261508
PMID:38877708
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11179496/
Abstract

Nocardia pyomyositis in immunocompetent patients is a rare occurrence. The diagnosis may be missed or delayed with the risk of progressive infection and suboptimal or inappropriate treatment. We present the case of a 48-year-old immunocompetent firefighter diagnosed with pyomyositis caused by acquired by direct skin inoculation from gardening activity. The patient developed a painful swelling on his right forearm that rapidly progressed proximally and deeper into the underlying muscle layer. Ultrasound imaging of his right forearm showed a 7-mm subcutaneous fluid collection with surrounding edema. Microbiologic analysis of the draining pus was confirmed to be by Matrix-Assisted Laser Desorption/Ionization Time-of-Flight (MALDI-TOF) Mass Spectrometry. After incision and drainage deep to the muscle layer to evacuate the abscess and a few ineffective antibiotic options, the patient was treated with intravenous ceftriaxone and oral linezolid for 6 weeks. He was then de-escalated to oral moxifloxacin for an additional 4 months to complete a total antibiotic treatment duration of 6 months. The wound healed satisfactorily and was completely closed by the fourth month of antibiotic therapy. Six months after discontinuation of antibiotics, the patient continued to do well with complete resolution of the infection. In this article, we discussed the risk factors for Nocardia in immunocompetent settings, the occupational risks for Nocardia in our index patient, and the challenges encountered with diagnosis and treatment. Nocardia should be included in the differential diagnosis of cutaneous infections, particularly if there is no improvement of "cellulitis" with traditional antimicrobial regimens and the infection extends into the deeper muscle tissues.

摘要

免疫功能正常患者的诺卡氏菌肌炎较为罕见。诊断可能会被遗漏或延迟,导致感染进展、治疗效果不佳或不当。我们报告了 1 例 48 岁免疫功能正常的消防员病例,他因直接皮肤接种园艺活动而感染诺卡氏菌,患有肌炎。患者右前臂出现疼痛性肿胀,迅速向近侧和深部肌肉层进展。右前臂超声检查显示 7mm 皮下积液伴周围水肿。引流脓液的微生物分析通过基质辅助激光解吸/电离飞行时间(MALDI-TOF)质谱法确认为诺卡氏菌。在肌肉层深部切开引流以排出脓肿和几种无效的抗生素选择后,患者接受头孢曲松静脉注射和口服利奈唑胺治疗 6 周。然后将其降级为口服莫西沙星治疗 4 个月,以完成总共 6 个月的抗生素治疗。伤口愈合良好,抗生素治疗第 4 个月完全闭合。抗生素停药 6 个月后,患者继续恢复良好,感染完全消退。本文讨论了免疫功能正常患者感染诺卡氏菌的危险因素、我们的指数患者感染诺卡氏菌的职业风险以及诊断和治疗中遇到的挑战。诺卡氏菌应纳入皮肤感染的鉴别诊断,特别是如果传统抗菌方案治疗“蜂窝织炎”没有改善且感染扩展到深部肌肉组织时。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad45/11179496/cc69abbffdfe/10.1177_23247096241261508-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad45/11179496/cc69abbffdfe/10.1177_23247096241261508-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad45/11179496/cc69abbffdfe/10.1177_23247096241261508-fig1.jpg

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本文引用的文献

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Invasive Nocardia Infections across Distinct Geographic Regions, United States.不同地理区域侵袭性诺卡菌感染,美国。
Emerg Infect Dis. 2023 Dec;29(12):2417-25. doi: 10.3201/eid2912.230673.
2
Primary Lymphocutaneous in an Immunocompetent Host: Case Report and Literature Review.原发性皮肤黏膜淋球菌感染 1 例报告并文献复习。
Medicina (Kaunas). 2022 Mar 28;58(4):488. doi: 10.3390/medicina58040488.
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Isolated Nocardiosis, an Unrecognized Primary Immunodeficiency?孤立性奴卡菌病,一种未被认识的原发性免疫缺陷病?
Front Immunol. 2020 Oct 20;11:590239. doi: 10.3389/fimmu.2020.590239. eCollection 2020.
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Intra-Abdominal Nocardiosis-Case Report and Review of the Literature.腹内诺卡菌病——病例报告及文献综述
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Nocardia infections in solid organ transplantation: Guidelines from the Infectious Diseases Community of Practice of the American Society of Transplantation.实体器官移植中的诺卡菌感染:美国移植学会实践感染病学组指南。
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Manifestations and outcomes of nocardia infections: Comparison of immunocompromised and nonimmunocompromised adult patients.诺卡菌感染的表现及结局:免疫功能低下与非免疫功能低下成年患者的比较
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