An unusual case of spontaneous pneumomediastinum: Case report

Anuttara Bhadra *, Najam Husain, Amir Rastegar, James Eccersley, Joshua Agilinko
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引用次数: 0

Abstract

Introduction

Spontaneous pneumomediastinum (SPM) is rare, with an incidence of 1/25,000. It is defined as extra luminal free air within the mediastinum, not associated with trauma. A classic clinical triad consists of pleuritic chest pain, dyspnoea and subcutaneous emphysema. SPM is self-limiting and symptoms can be managed conservatively. However despite a good prognosis, secondary causes should be excluded.

Case description

Miss AG, 27 year old with a known history of Ulcerative Colitis being treated with azathioprine and adalimumab, presented to the ED with a two week history of progressively worsening shortness of breath and left sided pleuritic chest pain. She reported a 3 day h/o ongoing fever, rigors for which she was being treated with Amoxicillin 500mg tds. The patient had no previous history of respiratory conditions and was a non-smoker. The patient saturated at 96% on 2L of Oxygen with a respiratory rate of 19. She was apyrexial, normotensive and acyanotic. Clinical findings on auscultation revealed left sided bronchial breathing, an erect postero-anterior chest x-ray revealed dense opacification throughout the left mid and lower zone. As she was increasingly symptomatic, she went onto have a CTPA, which showed a pneumomediastinum. A discussion with the thoracic surgeons followed and an urgent CT thorax and abdomen with oral gastrografin was carried out to exclude oesophageal perforation. This scan did not reveal any extravasation of contrast around the oesophagus to suggest a perforation or a leak. The patient improved clinically, discharged in 6 days, she was kept nil by mouth for 48 hours once the CT had confirmed that there was no perforation.

Results and Conclusions

SPM usually has a benign and favourable clinical course and is usually self-limiting. It is more commonly seen in young men. The pathophysiological process behind SPM was initially described by Macklin in 1944, who described a rupture of the terminal alveoli, secondary to pressure differences across the alveolar membrane causing air to leak into the lung interstitium and consequently into them mediastinum. In a retrospective study by Park et al., 44% of the patients had a precipitating factor, with the most common being cough.

Literature suggests that the most common symptoms reported in cases are usually chest pain, which is usually pleuritic in nature and dyspnoea Subcutaneous emphysema is also reported as common clinical sign and has a frequency ranging from 40% to 100% in cases. Moreover, the characteristic sign of systolic crackles on auscultation known as Hamman’s sign can also be heard in 30% of cases. Diagnosis in this case was made based on the CTPA though it is more commonly based on chest x-ray findings. Postero-anterior view establishes the diagnosis in about two-thirds of patients with the three commonest findings: air streaks in the superior mediastinum, prominent left sided silhouette of the heart and subcutaneous emphysema of the neck and shoulder. For this reason, a chest CT scan is a more conclusive and sensitive scan, which is considered the gold standard investigation for SPM. More importantly, a CT scan with an oral contrast, as in this case, will allow us to distinguish between secondary causes of a SPM such as an oesophageal leak or rupture. The prognosis is good and treatment is mainly conservative for those diagnosed. The average clinical course, reported in the retrospective study by Takada et al. was 1.8 days after diagnosis, with an average of 7.8 day of hospitalization. Complications such as hypertensive pneumomediastinum, pneumopericardium, and mediastinitis can occur and patients should be monitored throughout their admission.

Take home message

In conclusion, spontaneous pneumomediastinum is a rare condition, and is known to have a favourable clinical course, with symptoms of pleuritic chest pain and dyspnoea improving within a few days. Chest CT is the gold standard radiological investigation to confirm diagnosis whereby measures must be taken to exclude secondary causes of SPM. Patients can be treated conservatively and must be monitored for life threatening complications.

罕见自发性纵隔气肿1例
自发性纵隔气肿(SPM)是一种罕见的疾病,发病率为1/25,000。它被定义为纵隔内腔外的自由空气,与创伤无关。典型的临床三联征包括胸膜性胸痛、呼吸困难和皮下肺气肿。SPM是自限性的,症状可以保守处理。尽管预后良好,但应排除继发原因。病例描述:AG女士,27岁,有溃疡性结肠炎病史,正在接受硫唑嘌呤和阿达木单抗治疗,以两周进行性加重的呼吸短促和左侧胸膜炎性胸痛就诊。她报告持续发热3天,目前正在接受阿莫西林500mg tds治疗。患者既往无呼吸系统疾病史,不吸烟。患者血氧2L饱和96%,呼吸率19。她是直立的,血压正常,无生育。临床听诊显示左侧支气管呼吸,直立胸片显示左侧中下区致密混浊。随着症状的加重,她进行了CTPA检查,结果显示纵膈气肿。随后与胸外科医生进行了讨论,并在口服胃grafin的情况下进行了紧急胸腹CT检查,以排除食管穿孔。扫描未发现食道周围有造影剂外渗,提示有穿孔或渗漏。患者临床好转,6天后出院,CT确认无穿孔后留口48小时。结果与结论spm的临床病程通常为良性,且具有自限性。它更常见于年轻男性。SPM背后的病理生理过程最初是由Macklin在1944年描述的,他描述了终末肺泡破裂,继发于肺泡膜上的压力差,导致空气泄漏到肺间质,从而进入纵隔。在Park等人的回顾性研究中,44%的患者有诱发因素,最常见的是咳嗽。文献显示,病例中最常见的症状通常是胸痛,通常为胸膜炎性质,呼吸困难皮下肺气肿也被报道为常见的临床症状,在病例中发生率从40%到100%不等。此外,在30%的病例中也可以听到收缩期脆音的特征征象,即哈曼征象。本病例的诊断是基于CTPA,尽管更常见的是基于胸部x线检查结果。大约三分之二的患者的后前位检查通过以下三个最常见的表现来确诊:上纵隔气纹,左侧心脏轮廓突出,颈部和肩部皮下肺气肿。因此,胸部CT扫描是一种更具结论性和敏感性的扫描,被认为是SPM的金标准检查。更重要的是,CT扫描和口腔造影,如本例,将使我们能够区分SPM的继发原因,如食管渗漏或破裂。预后良好,确诊者以保守治疗为主。Takada等回顾性研究报告的平均临床病程为诊断后1.8天,平均住院时间为7.8天。高血压性纵隔气肿、心包气肿和纵隔炎等并发症可能发生,患者在入院期间应全程监测。总之,自发性纵隔气肿是一种罕见的疾病,已知其临床病程良好,胸膜炎性胸痛和呼吸困难症状可在几天内改善。胸部CT是确认诊断的金标准放射学检查,因此必须采取措施排除SPM的继发原因。患者可以保守治疗,必须监测是否有危及生命的并发症。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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