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Journal of rare diseases and orphan drugs最新文献

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A Case Report of Bullous Emphysema in an Adolescent: Congenital Malformation or Outcome of Bronchopulmonary Dysplasia? 青少年大疱性肺气肿1例:先天性畸形还是支气管肺发育不良的结局?
Pub Date : 2020-12-23 DOI: 10.36013/JRDOD.V2I.36
S. Ilchenko, A. Fialkovska, Oleksii Makoveychuk
Pulmonary emphysema belongs to the group of chronic obstructive pulmonary diseases, and inpediatric pulmonology is one of the complex diagnoses that require a careful differential diagnosis. Thearticle describes the possible causes of the formation and clinical manifestations of pulmonaryemphysema in children. We present a clinical case of bullous emphysema in a teenager. This case showsthat a detailed examination using such a modern diagnostic method as high-resolution computedtomography played a crucial role in establishing the patient's correct diagnosis. However, establishing thenature of this pathological process in the child was very difficult. Perhaps an earlier diagnosis couldprevent severe irreversible changes in a teenager's lungs would avoid developing the diffusebronchopulmonary process.
肺气肿属于慢性阻塞性肺疾病的一类,中间肺科是需要仔细鉴别诊断的复杂诊断之一。本文介绍了儿童肺气肿形成的可能原因及临床表现。我们报告一例青少年大疱性肺气肿的临床病例。该病例表明,使用高分辨率计算机断层扫描等现代诊断方法进行详细检查,在确定患者的正确诊断方面发挥了至关重要的作用。然而,在孩子身上确定这种病理过程的性质是非常困难的。也许早期诊断可以防止青少年肺部发生严重的不可逆变化,从而避免发展为弥漫性支气管肺过程。
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Journal of rare diseases and orphan drugs
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