Journal of Emergencies, Trauma, and Shock

CASE REPORT
Year
: 2013  |  Volume : 6  |  Issue : 2  |  Page : 138--139

The perils of sneezing: Bilateral spontaneous pneumothorax


Christina L Bourne 
 Department of Internal Medicine, Division of Emergency Medicine, Medical University of South Carolina, USA

Correspondence Address:
Christina L Bourne
Department of Internal Medicine, Division of Emergency Medicine, Medical University of South Carolina
USA

Abstract

This is a brief case report of an adolescent male who developed bilateral spontaneous pneumothorax after sneezing.



How to cite this article:
Bourne CL. The perils of sneezing: Bilateral spontaneous pneumothorax.J Emerg Trauma Shock 2013;6:138-139


How to cite this URL:
Bourne CL. The perils of sneezing: Bilateral spontaneous pneumothorax. J Emerg Trauma Shock [serial online] 2013 [cited 2019 Dec 15 ];6:138-139
Available from: http://www.onlinejets.org/text.asp?2013/6/2/138/110796


Full Text

 Introduction



Bilateral spontaneous pneumothorax is rare, but when it does occur is frequently life-threatening. This case illustrates the presentation of a bilateral spontaneous pneumothorax in a relatively asymptomatic individual.

 Case Report



A 15-year-old male with no reported past medical history presented to an urgent care with atraumatic chest pain. The pain was intermittent, sharp, pleuritic, substernal, and non-radiating. It started two days prior after sneezing. Review of symptoms was negative, specifically denying cough or dyspnea. One week prior, he had mild rhinorrhea and dry cough, which resolved. The patient denied smoking or illicit drug use. Vital signs were normal, including an oxygen saturation of 100% on room air. On examination, he appeared tall, thin, and acutely well. He was in no respiratory distress and lungs sounds were present, but slightly diminished bilaterally. There were no other remarkable examination findings. Chest X-ray study [Figure 1] and [Figure 2] showed spontaneous bilateral pneumothorax and evidence of surgical correction for pectus excavatum. The patient was admitted without intervention. Daily chest X-rays showed progressive improvement and he was discharged home four days later, after an uneventful hospital course.{Figure 1}{Figure 2}

A primary spontaneous pneumothorax is atraumatic without underlying evidence of lung disease and is common in young adults. [1] A bilateral spontaneous pneumothorax is very rare with a reported incidence of only 1.6% of cases of spontaneous pneumothorax. [2] Independent risk factors associated with bilateral spontaneous pneumothorax are lower weight, lower body mass index, higher height/weight ratio, and a higher frequency of blebs/bullae on high-resolution computed tomography. [2],[3] A secondary spontaneous pneumothorax is due to underlying pulmonary pathology. In this patient, collagen vascular disease including, Marfan's syndrome was considered. Surgical correction of pectus excavatum has been associated with pneumothorax, but within the peroperative period. [4]

 Discussion



Although rare, bilateral spontaneous pneumothorax is imperative to recognize and frequently leads to a life-threatening event. [2] This patient's benign presentation is unusual. Invasive treatment is often indicated in the acute setting as well as long-term to avoid recurrence. [5] High clinical suspicion and recognition of risk factors are critical.

References

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3Huang TW, Cheng YL, Tzao C, Hung C, Hsu HH, Chen JC, et al. Factors related to primary bilateral spontaneous pneumothorax. Thorac Cardiovasc Surg 2007;55:310-2.
4Nasr A, Fecteau A, Wales PW. Comparison of the Nuss and the Ravitch procedure for pectus excavatum repair: A meta-analysis. J Pediatr Surg 2010;45:880-6.
5O'Lone E, Elphick HE, Robinson PJ. Spontaneous pneumothorax in children: When is invasive treatment indicated? Pediatr Pulmonol 2008;43:41-6.