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婴儿因流感嗜血杆菌继发暴发性紫癜

Purpura Fulminans Secondary to Haemophilus influenzae in an Infant.

作者信息

Ko Amy, Mohammad Shanzay, Chandran Arjun, Donovan Summer D, Balakumar Niveditha

机构信息

Pediatrics, Baylor College of Medicine, Houston, USA.

Pediatrics, Christus Children's Hospital, San Antonio, USA.

出版信息

Cureus. 2025 May 1;17(5):e83313. doi: 10.7759/cureus.83313. eCollection 2025 May.

Abstract

Purpura fulminans (PF) is a hematological emergency that requires timely diagnosis for effective management. In this report, we discuss the case of a five-month-old previously healthy male who presented to the emergency department due to sudden-onset lethargy and rash in the setting of intermittent fevers, emesis, and diarrhea. Shortly after admission, the patient was noted to have rapidly progressive PF and was intubated due to impeding respiratory failure and hemodynamic instability requiring the institution of vasopressors and steroids for catecholamine-resistant, refractory septic shock. He was initially managed with a course of broad-spectrum antimicrobials, including ceftriaxone, doxycycline, and vancomycin, while awaiting the results from his blood and urine cultures. Unfortunately, our patient progressed to multi-organ failure and disseminated intravascular coagulation requiring advanced organ support, including the need for continuous renal replacement therapy. He was transferred to another facility for evaluation and continued management of his necrotic and gangrenous tissues, where he ultimately died after experiencing septic shock in the setting of bacteremia. Although blood and urine cultures were negative, his microbial cell-free DNA sequencing (Karius test) was positive for , the likely causal pathogen. is a Gram-negative coccobacillus that is commonly associated with invasive bacterial infections in the pediatric population. With the widespread implementation and utilization of the type B vaccine as part of routine vaccinations, the incidence of severe illness is rare. Only a handful of cases of causing PF are reported in the literature, and it is uncommon in the pediatric population, emphasizing the need to report and understand such occurrences. This case specifically highlights the importance of early recognition and timely management of PF, a rapidly degenerative clinical condition, in the setting of severe sepsis and multi-system organ failure secondary to an unlikely pathogen.

摘要

暴发性紫癜(PF)是一种血液学急症,需要及时诊断以进行有效治疗。在本报告中,我们讨论了一名5个月大的既往健康男性病例,该患儿因间歇性发热、呕吐和腹泻后突然出现嗜睡和皮疹而被送往急诊科。入院后不久,该患者被发现患有快速进展的PF,并因即将发生的呼吸衰竭和血流动力学不稳定而插管,由于对儿茶酚胺耐药的难治性感染性休克,需要使用血管加压药和类固醇。在等待血培养和尿培养结果期间,他最初接受了包括头孢曲松、多西环素和万古霉素在内的广谱抗菌药物治疗。不幸的是,我们的患者进展为多器官功能衰竭和弥散性血管内凝血,需要高级器官支持,包括持续肾脏替代治疗。他被转至另一机构评估和继续处理其坏死和坏疽组织,最终在菌血症导致的感染性休克后死亡。尽管血培养和尿培养均为阴性,但他的微生物无细胞DNA测序(Karius检测)对可能的致病病原体呈阳性。 是一种革兰氏阴性球杆菌,在儿科人群中通常与侵袭性细菌感染有关。随着B型疫苗作为常规疫苗接种的一部分广泛实施和应用,严重疾病的发病率很少见。文献中仅报道了少数几例 导致PF的病例,在儿科人群中并不常见,强调了报告和了解此类事件的必要性。该病例特别强调了在由不太可能的病原体引起的严重脓毒症和多系统器官衰竭背景下,早期识别和及时处理PF这种迅速恶化的临床病症的重要性。

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