Profir Irina, Popescu Cristina-Mihaela, Nechita Aurel
Faculty of Medicine and Pharmacy, "Dunărea de Jos" University of Galați, 800010 Galați, Romania.
"Sf. Ioan" Clinical Emergency Children's Hospital, 800487 Galați, Romania.
Children (Basel). 2025 Jun 13;12(6):766. doi: 10.3390/children12060766.
Influenza B usually causes mild illness in children. Severe and fatal cases can occur when complicated by secondary ( pneumonia, including community-acquired methicillin-resistant (MRSA). We present a rare, rapidly progressive fatal case in an adolescent with no known medical history to highlight diagnostic and therapeutic pitfalls.
A 16-year-old boy with no known underlying conditions (unvaccinated for influenza) presented critically ill at "Sf. Ioan" Clinical Emergency Pediatric Hospital in Galați after one week of high fever and cough. He was in respiratory failure with septic shock, requiring immediate intubation and vasopressors. Chest X-ray (CXR) showed diffuse bilateral infiltrates (acute respiratory distress syndrome, ARDS). Initial laboratory tests revealed leukopenia, severe thrombocytopenia, disseminated intravascular coagulation (DIC), rhabdomyolysis, and acute kidney injury (AKI). Reverse transcription polymerase chain reaction (RT-PCR) confirmed influenza B, and blood cultures grew MRSA. Despite maximal intensive care, including mechanical ventilation, antibiotics (escalated for MRSA), antiviral therapy, and cytokine hemoadsorption therapy, the patient developed refractory multi-organ failure and died on hospital day 6. Autopsy revealed bilateral necrotizing pneumonia (NP) without radiographic cavitation, underscoring the diagnostic challenge.
The initial chest radiography showed diffuse bilateral pulmonary infiltrates, predominantly in the lower zones, with an ill-defined, patchy, and confluent appearance. Such appearance, in our case, was more suggestive of rapid progressive NP caused by MRSA rather than the typical pneumococcal one. This is one of the few reported cases of influenza B-MRSA coinfection with fulminant rhabdomyolysis and autopsy-confirmed necrosis. Our fulminant case illustrates the synergistic virulence of influenza and MRSA. Toxin-producing MRSA strains can cause NP and a "cytokine storm," causing capillary leak, ARDS, shock, and DIC. Once multi-organ failure ensues, the prognosis is grim despite aggressive care. The absence of early radiographic necrosis and delayed anti-MRSA therapy (initiated after culture results) likely contributed to the poor outcome.
Influenza B-MRSA co-infection, though rare, demands urgent empiric anti-MRSA therapy in severe influenza cases with leukopenia or shock, even without radiographic necrosis. This fatal outcome underscores the dual imperative of influenza vaccination and early, aggressive dual-pathogen targeting in high-risk presentations.
乙型流感通常在儿童中引起轻症。当并发继发性(肺炎,包括社区获得性耐甲氧西林金黄色葡萄球菌(MRSA)感染)时,可出现严重及致命病例。我们报告一例罕见的、进展迅速的致命病例,患者为一名无已知病史的青少年,以突出诊断和治疗中的陷阱。
一名16岁男孩,无已知基础疾病(未接种流感疫苗),在高热和咳嗽一周后,以危重症状态被送至加拉茨的“圣伊万”临床急诊儿童医院。他出现呼吸衰竭并伴有感染性休克,需要立即插管并使用血管活性药物。胸部X线(CXR)显示双侧弥漫性浸润(急性呼吸窘迫综合征,ARDS)。初始实验室检查显示白细胞减少、严重血小板减少、弥散性血管内凝血(DIC)、横纹肌溶解和急性肾损伤(AKI)。逆转录聚合酶链反应(RT-PCR)确诊为乙型流感,血培养分离出MRSA。尽管给予了最大程度的重症监护,包括机械通气、抗生素(针对MRSA升级用药)、抗病毒治疗和细胞因子血液吸附治疗,但患者仍出现难治性多器官功能衰竭,并于住院第6天死亡。尸检显示双侧坏死性肺炎(NP),无影像学空洞形成,凸显了诊断挑战。
初始胸部X线显示双侧弥漫性肺部浸润,主要位于下肺区,表现为边界不清、斑片状和融合状。在我们的病例中,这种表现更提示由MRSA引起的快速进展性NP,而非典型的肺炎球菌肺炎。这是少数报道的乙型流感-MRSA合并感染伴暴发性横纹肌溶解且经尸检证实坏死的病例之一。我们的暴发性病例说明了流感和MRSA的协同毒力。产毒素的MRSA菌株可导致NP和“细胞因子风暴”,引起毛细血管渗漏、ARDS、休克和DIC。一旦发生多器官功能衰竭,尽管积极治疗,预后仍很严峻。早期影像学无坏死表现以及抗MRSA治疗延迟(培养结果出来后才开始)可能导致了不良结局。
乙型流感-MRSA合并感染虽罕见,但在严重流感伴有白细胞减少或休克的病例中,即使无影像学坏死表现,也需要紧急经验性抗MRSA治疗。这一致命结局凸显了流感疫苗接种以及在高危病例中早期、积极针对双重病原体治疗的双重必要性。