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一名患有未知免疫疾病的儿科患者的鉴别诊断与多学科检查:病毒感染继发的慢性呼吸窘迫及发育后果

Differential Diagnosis and Interdisciplinary Workup of a Pediatric Patient With an Unknown Immune Condition: Chronic Respiratory Distress Secondary to Viral Illness and Developmental Consequences.

作者信息

Daidone Camryn, Carper Sheyenne

机构信息

Research, Edward Via College of Osteopathic Medicine, Shreveport, USA.

Pediatrics, Willis-Knighton Health System, Shreveport, USA.

出版信息

Cureus. 2024 Jan 28;16(1):e53109. doi: 10.7759/cureus.53109. eCollection 2024 Jan.

Abstract

We present a case of a three-year-old African American male, born at term, who initially presented with bronchiolitis at six months and has since experienced recurrent episodes of respiratory distress and hospitalizations. The patient also has severe eczema, developmental delays, and recurrent viral illnesses. Despite thorough evaluations from various specialists, such as pulmonology, allergy, and gastroenterology, the underlying cause remained elusive. The differential diagnosis for this case is as follows: severe persistent asthma with a possible link to genetic mutations such as CDHR3, hyper-IgE syndrome, atypical presentation of Wiskott-Aldrich syndrome, and severe gastroesophageal reflux disease (GERD) with aspiration pneumonitis. This patient's chronic condition has contributed to several developmental consequences, including failure to gain weight and possible hypoxic encephalopathy, leading to delays in cognitive and motor milestones and speech delays. Aggressive medical management, especially long-term systemic steroids, raises concerns about future complications. Through this case, we highlight the importance of thorough workups and an interdisciplinary approach to diagnosing and managing an unknown immune condition, as well as consistent pediatric primary care follow-up to assess development and coordinate necessary support. Here, we aim to address a gap in research on the unique presentations of pediatric respiratory distress symptoms by formulating a comprehensive differential diagnosis and exploring the various ways that chronic respiratory illness can contribute to developmental deficits such as speech and cognitive delays in pediatric patients. This study calls for further research into genetic contributions to asthma, diverse presentations of GERD, prevention of viral illnesses, alternative treatments minimizing steroid use, and an understanding of the impact of chronic respiratory distress on cognitive and language development in children. Thorough workups and interdisciplinary approaches are essential for effective diagnosis and management.

摘要

我们报告一例足月出生的三岁非裔美国男性病例,该患儿六个月大时最初表现为细支气管炎,此后反复出现呼吸窘迫发作并住院治疗。该患者还患有严重湿疹、发育迟缓以及反复的病毒感染。尽管接受了来自肺科、过敏科和胃肠病科等不同专科医生的全面评估,但其潜在病因仍不明确。该病例的鉴别诊断如下:重度持续性哮喘,可能与CDHR3等基因突变有关;高免疫球蛋白E综合征;维斯科特-奥尔德里奇综合征的非典型表现;以及伴有吸入性肺炎的严重胃食管反流病(GERD)。该患者的慢性疾病导致了多种发育后果,包括体重不增以及可能的缺氧性脑病,进而导致认知和运动发育里程碑延迟以及语言发育迟缓。积极的药物治疗,尤其是长期使用全身性类固醇,引发了对未来并发症的担忧。通过这个病例,我们强调了全面检查以及采用跨学科方法来诊断和管理不明免疫状况的重要性,以及持续的儿科初级保健随访以评估发育情况并协调必要支持的重要性。在此,我们旨在通过制定全面的鉴别诊断并探索慢性呼吸道疾病导致儿科患者语言和认知延迟等发育缺陷的各种方式,来填补儿科呼吸窘迫症状独特表现研究方面的空白。本研究呼吁进一步开展关于哮喘的遗传因素、GERD的多样表现、病毒感染的预防、减少类固醇使用的替代治疗方法,以及了解慢性呼吸窘迫对儿童认知和语言发育影响的研究。全面检查和跨学科方法对于有效诊断和管理至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ad4/10898650/bc59641dcc92/cureus-0016-00000053109-i01.jpg

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