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一例罕见的继发于停乳链球菌败血症的青少年会厌炎病例。

A Rare Case of Adolescent Epiglottitis Secondary to Streptococcus dysgalactiae Septicemia.

作者信息

Tilak Kedar, Abdul Ghayum Mohamed Aashiq, Swanson Douglas, El Feghaly Rana

机构信息

Neonatology and Pediatric Infectious Diseases, Children's Mercy Kansas City, Kansas City, USA.

Pediatric Cardiology, Children's Mercy Kansas City, Kansas City, USA.

出版信息

Cureus. 2025 Feb 7;17(2):e78671. doi: 10.7759/cureus.78671. eCollection 2025 Feb.

DOI:10.7759/cureus.78671
PMID:40062022
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11890568/
Abstract

()is a relatively uncommon pathogen in the pediatric populations, often overshadowed by ()in causing diseases such as cellulitis, severe seep tissue necrotizing infections, and streptococcal toxic shock syndrome. This case report presents the case of a 15-year-old recent immigrant male patient from Egypt who developed an extensive neck infection with complications from septicemia. Initially misdiagnosed as viral pharyngitis, the patient was later admitted with high fevers, dysphagia, and progressive respiratory distress. Imaging revealed widespread inflammatory changes, including cellulitis, epiglottitis, and lymphadenopathy. Despite prompt antibiotic therapy, the patient required critical interventions, including intubation, inotropic support, followed by a tracheostomy. Blood cultures confirmed leading to tailored antibiotic therapy adjustments. This case underscores the pathogen's potential to cause severe infections in pediatric patients, highlighting the need for early recognition and aggressive management. The clinical spectrum and burden of remain underexplored, requiring further study to clarify its pathophysiology and infection patterns. Though rare in pediatric cases, particularly life-threatening septicemia, this organism should be considered alongside in severe infections.

摘要

()在儿科人群中是一种相对不常见的病原体,在引起蜂窝织炎、严重深部组织坏死性感染和链球菌中毒性休克综合征等疾病方面,常被()掩盖。本病例报告介绍了一名来自埃及的15岁近期移民男性患者,他发生了广泛的颈部感染并伴有败血症并发症。该患者最初被误诊为病毒性咽炎,后来因高热、吞咽困难和进行性呼吸窘迫入院。影像学检查显示广泛的炎症改变,包括蜂窝织炎、会厌炎和淋巴结病。尽管及时进行了抗生素治疗,但患者仍需要进行包括插管、使用血管活性药物支持,随后进行气管切开等关键干预措施。血培养确诊为(),从而进行了针对性的抗生素治疗调整。本病例强调了该病原体在儿科患者中引起严重感染的可能性,突出了早期识别和积极管理的必要性。()的临床谱和负担仍未得到充分研究,需要进一步研究以阐明其病理生理学和感染模式。尽管在儿科病例中罕见,尤其是危及生命的败血症,但在严重感染中应将这种病原体与()一并考虑。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/688c/11890568/fbf38d6a6b11/cureus-0017-00000078671-i03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/688c/11890568/3d70ace981ca/cureus-0017-00000078671-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/688c/11890568/cd872740827a/cureus-0017-00000078671-i02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/688c/11890568/fbf38d6a6b11/cureus-0017-00000078671-i03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/688c/11890568/3d70ace981ca/cureus-0017-00000078671-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/688c/11890568/cd872740827a/cureus-0017-00000078671-i02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/688c/11890568/fbf38d6a6b11/cureus-0017-00000078671-i03.jpg

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Neuropsychiatric Disorder Associated with Group G Infection.
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