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社区获得性耐甲氧西林金黄色葡萄球菌侵袭性感染表现为脓毒性血管炎:一例儿科病例报告

Septic Vasculitis as a Manifestation of Invasive Infection by Community-Acquired Methicillin-Resistant Staphylococcus aureus: A Pediatric Case Report.

作者信息

Campos Ana

机构信息

Pediatrics, Universidad de Valparaíso, Valparaíso, CHL.

Pediatrics, Hospital Gustavo Fricke, Viña del Mar, CHL.

出版信息

Cureus. 2025 Aug 27;17(8):e91135. doi: 10.7759/cureus.91135. eCollection 2025 Aug.

DOI:10.7759/cureus.91135
PMID:41018302
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12470508/
Abstract

Septic vasculitis (SV) is an uncommon complication of bacterial sepsis, characterized by inflammation and thrombosis of small- and medium-sized blood vessels. Although it is most often associated with meningococcemia, cases linked to have been reported. Presented is the case of a previously healthy adolescent who developed SV as an initial manifestation of community-acquired methicillin-resistant (CA-MRSA) bacteremia. The patient presented with fever, abdominal pain, and purpuric skin lesions, without any known exposure to typical risk factors. Initial clinical suspicion included loxoscelism, a necrotic arachnidism caused by spider bites, based on initial skin lesion morphology. However, further evaluation ruled out loxoscelism and autoimmune etiologies. Subsequent investigations confirmed MRSA infection through blood cultures, while skin biopsy revealed histological features of cutaneous vasculitis, establishing the diagnosis of SV. Imaging identified secondary infectious foci in the spleen, kidneys, and bone, though no surgical intervention was necessary. The case was managed with targeted antibiotic therapy, resulting in complete clinical recovery. This case underscores the importance of recognizing SV as a rare but serious initial manifestation of invasive bacterial infection in children and highlights the diagnostic value of skin findings in febrile illnesses, emphasizing the need for prompt and comprehensive etiological investigation.

摘要

脓毒性血管炎(SV)是细菌性败血症的一种罕见并发症,其特征为中小血管的炎症和血栓形成。虽然它最常与脑膜炎球菌血症相关,但也有与其他病因相关的病例报道。本文介绍了一例既往健康的青少年病例,该患者以脓毒性血管炎作为社区获得性耐甲氧西林金黄色葡萄球菌(CA-MRSA)菌血症的初始表现。患者出现发热、腹痛和紫癜性皮肤病变,无任何已知的典型危险因素暴露史。基于初始皮肤病变形态,最初的临床怀疑包括洛矶山蜘蛛毒中毒,这是一种由蜘蛛叮咬引起的坏死性蛛毒中毒。然而,进一步评估排除了洛矶山蜘蛛毒中毒和自身免疫性病因。随后的调查通过血培养确诊为MRSA感染,而皮肤活检显示皮肤血管炎的组织学特征,从而确立了脓毒性血管炎的诊断。影像学检查在脾脏、肾脏和骨骼中发现了继发性感染灶,不过无需手术干预。该病例采用针对性抗生素治疗,临床完全康复。本病例强调了认识到脓毒性血管炎是儿童侵袭性细菌感染罕见但严重的初始表现的重要性,并突出了皮肤表现在发热性疾病中的诊断价值,强调了及时进行全面病因调查的必要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9ad9/12470508/32f61ebb5ada/cureus-0017-00000091135-i02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9ad9/12470508/239f3dce61d7/cureus-0017-00000091135-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9ad9/12470508/32f61ebb5ada/cureus-0017-00000091135-i02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9ad9/12470508/239f3dce61d7/cureus-0017-00000091135-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9ad9/12470508/32f61ebb5ada/cureus-0017-00000091135-i02.jpg

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Invasive Community-Acquired Methicillin-Resistant Staphylococcus aureus With Aortic Aneurysm in a 10-Year-Old Patient: A Case Report.一名10岁患者侵袭性社区获得性耐甲氧西林金黄色葡萄球菌感染合并主动脉瘤:病例报告
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