所有喘气的东西都不是哮喘:一个病例报告。

IF 1.1 4区 医学 Q4 ALLERGY Pediatric Allergy Immunology and Pulmonology Pub Date : 2021-09-01 Epub Date: 2021-06-18 DOI:10.1089/ped.2021.0006
Sagar K Shah, Natalie Sabzghabaei
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引用次数: 0

摘要

背景:本病例报告为儿科医生提供了一种罕见疾病的独特表现。塑性支气管炎(PB)是一种非常罕见的疾病,表现为支气管树内形成铸型。这通常发生在接受过修复的先天性心脏缺陷患者中,然而,在其他健康患者中并不常见。甲型流感、淋巴异常和单心室生理是唯一被证实的PB病因。然而,哮喘、毒性吸入和急性胸综合征是许多已被提出的使患者易患PB的条件中的少数几种。病例介绍:因此,讨论一个9岁男孩的病例是很重要的,他有不受控制的哮喘病史,表现为咳嗽、发冷、体重减轻和发烧。由于担心坏死性肺炎,患者最初使用广谱抗生素治疗,但由于改善失败,进行了直接喉镜和支气管镜检查,诊断为PB。尽管该患者有未控制的哮喘病史,但这是唯一使其有患PB风险的易感呼吸系统疾病。该患者继续接受皮质类固醇、胸部物理治疗、吸入纤维蛋白溶解剂和直接纤维蛋白溶解治疗,症状和影像学明显改善。结论:PB虽然罕见,但当患者出现病因不明的呼吸道症状时,所有儿科医生都必须牢记。对PB患者的诊断和治疗的延误可能是有害的,因为这些铸型的咳痰可导致窒息和死亡。这篇文章继续提醒所有的医生,在所有级别,进行彻底的病史/身体检查,创建一个广泛的鉴别,并全面治疗每个病人的重要性。
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Everything That Wheezes Is Not Asthma: A Case Report.

Background: This case report provides the general pediatrician with insight on a unique presentation of an already rare disease. Plastic bronchitis (PB) is an exceedingly rare disease that presents with the formation of casts in the endobronchial tree. This typically occurs in patients with congenital heart defects that have undergone repair, however, it is atypical to be seen in otherwise healthy patients. Influenza A, lymphatic abnormalities, and single ventricle physiology are the only proven causes of PB. Asthma, toxic inhalation, and acute chest syndrome, however, are a few of the many conditions that have been proposed to predispose patients toward developing PB. Case Presentation: Thus, it is important to discuss the case of a 9-year-old boy with a history of uncontrolled asthma who presented with cough, chills, weight loss, and fevers. This patient was initially treated with broad-spectrum antibiotics due to concerns for necrotizing pneumonia, but due to failure in improvement, a direct laryngoscopy and bronchoscopy was performed, revealing the diagnosis of PB. Although this patient had a history of uncontrolled asthma, this was the only predisposing respiratory condition that put him at risk of developing PB. This patient went on to be treated with corticosteroids, chest physiotherapy, inhaled fibrinolytics, and direct fibrinolytic therapy with marked improvement in symptoms and imaging. Conclusion: PB, though rare, is a condition that all pediatricians must keep in their minds when patients present with respiratory symptoms with an unclear etiology. The delay in diagnosis and treatment of patients with PB can be detrimental as expectoration of these casts can result in asphyxiation and death. This article goes on to remind all providers, at all levels, the importance of conducting a thorough history/physical examination, creating a broad differential, and treating each patient holistically.

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来源期刊
CiteScore
2.00
自引率
0.00%
发文量
23
审稿时长
>12 weeks
期刊介绍: Pediatric Allergy, Immunology, and Pulmonology is a peer-reviewed journal designed to promote understanding and advance the treatment of respiratory, allergic, and immunologic diseases in children. The Journal delivers original translational, clinical, and epidemiologic research on the most common chronic illnesses of children—asthma and allergies—as well as many less common and rare diseases. It emphasizes the developmental implications of the morphological, physiological, pharmacological, and sociological components of these problems, as well as the impact of disease processes on families. Pediatric Allergy, Immunology, and Pulmonology coverage includes: -Functional and genetic immune deficiencies- Interstitial lung diseases- Both common and rare respiratory, allergic, and immunologic diseases- Patient care- Patient education research- Public health policy- International health studies
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