Tortajada-Girbés Miguel, Moreno-Prat Miriam, Ainsa-Laguna David, Mas Silvia
Department of Pediatrics, Dr. Peset University Hospital, Valencia, Spain; Department of Pediatrics, Obstetrics and Gynecology, University of Valencia, Av. Gaspar, Aguilar, 90. 46017 Valencia, Spain
Luis Oliag Health Centre Valencia, Departament of Valencia Dr. Peset, Valencia, Spain.
Ther Adv Respir Dis. 2016 Oct;10(5):402-9. doi: 10.1177/1753465816657478. Epub 2016 Sep 1.
Spontaneous pneumomediastinum (SPM) is an uncommon disorder. It is rarely reported in paediatric patients and may be accompanied by subcutaneous emphysema. It is usually benign and self-limiting, with only supportive therapy being needed, but severe cases may require invasive measures. Asthma exacerbations have classically been described as a cause of SPM. However, detailed descriptions in asthmatic children are scarce. We aimed at improving the current understanding of the features of SPM and subcutaneous emphysema, and outcomes, by means of a case report and a systematic review.
For the systematic review a literature search was performed in PubMed to identify reported cases of SPM in asthmatic children.
The case a 10-year-old asthmatic girl with SPM is reported. The patient received an inhaled corticosteroid and long-acting beta2 agonist, in addition to sublingual immunotherapy (SLIT) with eventual control of asthma symptoms.
A total of 114 published cases were found since 1995, most of them in teenagers; no sex differences were observed. Clinical presentation was associated with an asthma exacerbation in a number of cases. Other presenting features were chest pain, dyspnoea, cough, and particularly acute swelling of the face, neck, and upper chest. Subcutaneous emphysema was present in most patients. Overall, three cases of pneumothorax and two cases of pneumorrhachis were reported. Therapy was mainly based on supportive care, rest, oxygen therapy, analgesics, steroids, and bronchodilators. All patients recovered spontaneously, in spite of a small initial increase in SPM in a few cases.
Early identification of patients at risk of SPM would avoid the high number of under-diagnosed cases. Patients should be treated not only with supportive therapy but also with measures to achieve control of the underlying cause (such as poorly controlled asthma).
自发性纵隔气肿(SPM)是一种罕见的疾病。在儿科患者中很少有报道,可能伴有皮下气肿。它通常是良性的且具有自限性,仅需支持性治疗,但严重病例可能需要采取侵入性措施。哮喘发作一直被经典地描述为SPM的一个病因。然而,关于哮喘儿童的详细描述却很稀少。我们旨在通过病例报告和系统评价来提高目前对SPM和皮下气肿的特征以及结局的认识。
为进行系统评价,在PubMed上进行文献检索,以确定哮喘儿童中报道的SPM病例。
报告了一例10岁患有SPM的哮喘女孩病例。该患者接受了吸入性糖皮质激素和长效β2受体激动剂治疗,此外还接受了舌下免疫治疗(SLIT),最终哮喘症状得到控制。
自1995年以来共发现114例已发表的病例,其中大多数为青少年;未观察到性别差异。在许多病例中,临床表现与哮喘发作有关。其他表现特征包括胸痛、呼吸困难、咳嗽,尤其是面部、颈部和上胸部的急性肿胀。大多数患者存在皮下气肿。总体而言,报告了3例气胸和2例脊髓积气。治疗主要基于支持性护理、休息、吸氧、止痛、使用类固醇和支气管扩张剂。尽管少数病例最初SPM略有增加,但所有患者均自发康复。
早期识别有SPM风险的患者可避免大量漏诊病例。对患者不仅应进行支持性治疗,还应采取措施控制潜在病因(如控制不佳的哮喘)。