Case Reports in Pulmonology
Volume 2019 (2019), Article ID 5359309, 5 pages
https://doi.org/10.1155/2019/5359309

Case Report

An Unusual Cause of Spontaneous Pneumomediastinum: The Mounier-Kuhn Syndrome

Salim Naciri, Rachida Zahraoui, Mouna Soualhi, and Jamal-Eddine Bourkadi

Moulay Youssef Hospital, Pulmonary Unit, University Mohammed V of Rabat, Morocco

Correspondence should be addressed to Salim Naciri; naciri_salim@hotmail.com

Received 2 May 2019; Accepted 1 July 2019; Published 8 July 2019

Academic Editor: Akif Turna

Copyright © 2019 Salim Naciri et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract.

Mounier-Kuhn syndrome is a rare clinical and radiologic condition. It is characterized by tracheal and bronchial dilation. Diagnosis is made by computed tomography and bronchoscopy. An 81-year-old man presenting with an acute chest pain was referred to the pulmonology department. His chest computed tomographic scan showed a tracheobronchomegaly with an increase in the diameter of both the trachea and right and left main bronchi, associated with pneumomediastinum and fibrosis. Fiberoptic bronchoscopy revealed enlarged trachea and both main bronchi. These findings are consistent with a diagnosis of Mounier-Kuhn syndrome. Besides considering this long-neglected “orphan disease” when diagnosing spontaneous pneumomediastinum, clinicians should also be aware of an underlying Mounier-Kuhn syndrome in patients with recurrent respiratory infections, in order to avoid complications associated with the disease.

1. Introduction

Mounier-Kuhn syndrome (MKS) or congenital tracheobronchomegaly is a rare clinical and radiologic condition. It is characterized by tracheal and bronchial dilation [1]. Histology shows loss of the main airway smooth muscle and cartilage and an associated tracheal diverticulosis, but its etiology remains uncertain. Dilation of the trachea and proximal bronchi is associated with a decreased mucociliary clearance, airway inflammation, inefficient cough and bronchiectasis, and/or emphysema [2]. Rare cases of spontaneous pneumothorax have been reported, but only one case was related to a spontaneous pneumomediastinum.

2. Case Presentation

An 81-year-old man presenting with an acute chest pain was referred to the pulmonology department. He had no smoking history but recurrent respiratory infections.

The physical examination revealed that the patient was in good general health, with tachypnea at rest. The examination of patient’s chest revealed the presence of bilateral rales, more on basal regions.

Labs were unremarkable except for arterial blood gas that noted a decline in respiratory function (PaO2=63mmHg) (Table 1).

Table 1: Patient blood results.

Blood test
Blood count
Serum electrolytes
Others

Results
Hemoglobin=14,2g/dL
Na+=138mmol/L
Liver enzymes, urea, creatinine: without any particularities

White Cells=5490 elements/mm3
K+=4,20mmol/L

Platelets =247000/mm3
Glucose=1,0 g/L

C Reactive Protein=7

Blood test
Arterial blood gas
Arterial blood gas control

Results
pH=7,39
pH=7,4

PaO2=63mmHg
PaO2=65mmHg

PaCO2=44mmHg
PaCO2=42mmHg

SaO2=93%
SaO2=94%

Enlargement of the trachea and a pneumomediastinum were detected in the chest radiograph (Figure 1). The chest computed tomographic (CT) scan showed tracheobronchomegaly with an increase in the transverse diameter of the trachea and right and left main bronchi measured at 32, 26, and 25 mm, respectively (Figure 2). Bronchiectasis was noted in the bilateral lungs, bullous emphysema was noted in the bilateral upper lobes, and fibrosis was detected in the bilateral lower lobes (Figure 3).

Figure 1: Chest X-ray showing tracheal and proximal bronchi dilation (red arrows) and pneumomediastinum (blue arrows).

Figure 2: CT scan showing tracheal and both main bronchi dilation with associated pneumomediastinum.

Figure 3: CT scan showing bronchiectasis, bullous emphysema, and fibrosis.

Fiberoptic bronchoscopy revealed tracheal dilation and enlargement of both main bronchi.

The bronchoscopy findings coupled with the findings on CT chest confirmed a diagnosis of MKS.

The patient made good progress with high flow oxygenotherapy administered for 8 days, and the pneumomediastinum remitted in the control CT scan (Figure 4). The patient was discharged and followed up in an outpatient setting. The arterial blood gas control (Table 1) confirmed the decline in respiratory function, and pulmonary function testing revealed moderate airflow obstruction.

Figure 4: Control CT scan showing regression of the pneumomediastinum.

3. Discussion

The syndrome was first described by Mounier Kuhn in 1932. It is characterized by a dilation of the trachea and main bronchi due to laxity to the walls of the airway with decreased mucociliary clearance [2, 3]. This leads to formation of diverticula and bronchiectasis and recurrent infections. The prevalence is relatively low, affecting between 1% and 4.5% of the population and generally presents in the third or fourth decade of life [4–7]. There is a strong male predominance (about 8:1) [6, 7] and most of the patients seem to be smokers. Non-smokers have also been reported [2] like our presentation of an 81-year-old man non-smoker with a long history of respiratory symptoms.

Radiologic diagnosis can be established with plain chest radiograph alone [2] but CT has become the golden standard for confirming the diagnosis [8] by giving abnormal airway measurement (increase in the tracheal transverse diameter, right and left main bronchi upper than 3 cm, 2,4 cm, and 2,3cm, respectively, in adults) and may additionally demonstrate associated pathology. Krustins’ analysis of 128 published cases between 1987 and 2013 revealed the presence of tracheal diverticulosis in 33% of patients with this syndrome [9]. However, our patient’s CT scan revealed enlargement of trachea and both main bronchi and also bronchiectasis, emphysema, and pulmonary fibrosis.

Although some patients have no smoking history, as in our case, the association with COPD is frequently reported in 48,5% over 33 patients who had lung function test results in Krustins’ study [9]. The relationship between MKS and COPD remains unclear.

Most frequent pulmonary complications quoted in literature are bronchiectasis (49,2%), bullous emphysema, recurrent pneumonia, and aspergillosis [9–12]. Fibrosis and decline in respiratory function are also described in some reports like a series of eleven cases [13] which reported complications as bronchiectasis in 54% and one case of parenchymal fibrosis, as in our presentation. Another case of fibrosis complicating the MKS was also described in an eight-case series [7].

We are aware of only two cases presenting initially with spontaneous pneumothorax [5, 14], and to the best of our knowledge, only one research in the literature has reported MKS being a possible cause of spontaneous pneumomediastinum [15]. The case reported by Simkins was about a 95-year-old man with spontaneous pneumomediastinum and pneumonia.

The most likely pathophysiological mechanism involved in the genesis of pneumomediastinum in our case would be the existence of a decreasing pressure gradient between the alveoli and the lung interstitium that can result in alveolar rupture. Another possible explanation for pneumomediastinum is the abnormal increase of pressure in the mediastinum, like in a context of vigorous coughing, for example, that could cause the rupture of tracheal diverticula, frequently encountered in MKS [13]. In the case described by Simkins, the mechanism was related to oesophageal perforation [15].

The described case report offers a rare insight into the natural course of the progression of an undiagnosed MKS. Factors affecting disease progression in patients have not been studied; therefore the prognosis of patients with MKS is largely unknown [9].

This case supports early diagnosis in patients with MKS so that a decline in respiratory function resulting from possible complications of MKS may be prevented.

4. Conclusion

Mounier-Kuhn syndrome or tracheobronchomegaly is a very rare condition whose congenital or acquired origin is still controversial. The fact that clinical signs are not very specific should be considered as a differential diagnosis in patients with pneumomediastinum, even if the association is very rare as our case is the second reported in literature. The radiological diagnosis is easy, based on a careful analysis of the central airways and pulmonary parenchyma by CT examination. However, more studies have to be carried out to understand the etiology and natural course of this orphan disease.

Abbreviations

CT: | Computed tomography
MKS: | Mounier-Kuhn syndrome
COPD: | Chronic obstructive pulmonary disease.

Consent

A written informed consent was obtained from the patient for the publication of this case report and any accompanying images.

Disclosure

This case report was written based on clinical observation without any funding.

Conflicts of Interest

There are no conflicts of interest between the authors and between the authors and the patient.

Authors’ Contributions

Salim Naciri drafted this manuscript under Rachida Zahraoui’s supervision. Mouna Soualhi and Jamal-Eddine Bourkadi have been involved in drafting the manuscript. All authors read and approved the final manuscript.

References

I. Katz, M. Levine, and P. Herman, “Tracheobronchiomegaly. The Mounier-Kuhn syndrome,” The American Journal of Roentgenology Radium Therapy and Nuclear Medicine, vol. 88, Article ID 1084e94, 1962.

J. H. Woodring, R. S. Howard, and S. R. Rehm, “Congenital tracheo- bronchomegaly (Mounier-Kuhn syndrome): a report of 10 cases and review of the literature,” Journal of Thoracic Imaging, vol. 6, no. 2, pp. 1–10, 1991.

F. A. Khasawneh and A. J. Jou-Tindo, “A 30-year-old woman with recurrent lower respiratory tract infections,” Chest, vol. 143, no. 5, pp. 1500–1503, 2013.

F. P. Fortuna, K. IrionII, C. WinkIII, and J. L. BoemoI, “Mounier-Kuhn syndrome,” Jornal Brasileiro de Pneumologia, vol. 32, pp. 180–183, 2006.

B. D. Kent, I. Sulaiman, N. B. Akasheh, P. Nadarajan, E. Moloney, and S. J. Lane, “An unusual cause of spontaneous pneumothorax: the Mounier-Kuhn syndrome,” Irish Medical Journal, vol. 104, no. 5, pp. 152-153, 2011.

R. F. Johnston and R. A. Green, “Tracheobronchiomegaly. Report of Five cases and demonstration of familial occurrence,” American Review of Respiratory Disease, vol. 91, no. 1, pp. 35–50, 1965.

B. Menon, B. Aggarwal, and A. Iqbal, “Mounier-Kuhn syndrome: report of 8 cases of tracheobronchomegaly with associated complications,” Southern Medical Journal, vol. 101, no. 1, pp. 83–87, 2008.

M. G. Dunne and B. Reiner, “CT Features of Tracheobronchomegaly,” Journal of Computer Assisted Tomography, vol. 12, no. 3, pp. 388–391, 1988.

E. Krustins, “Mounier-Kuhn syndrome: A systematic analysis of 128 cases published within last 25 years,” The Clinical Respiratory Journal, vol. 10, no. 1, pp. 3–10, 2016.

C. Quentin, N. Lefevre, E. Bodart et al., “Mounier kuhn syndrome presenting with recurrent atelectasis,” Insights in Chest Diseases, vol. 1, no. 3, 2016.

R. Akgedik, C. E. Dagli, A. B. Kurt, H. Ozturk, and N. Tas, “The association of Mounier-Kuhn syndrome and pulmonary aspergillomas: a case report,” Balkan Medical Journal, vol. 33, no. 5, pp. 585-586, 2016.

J. G. Ayres, F. M. Pope, J. F. Reidy, and T. J. Clark, “Abnormalities of the lungs and thoracic cage in the Ehlers-Danlos syndrome,” Thorax, vol. 40, no. 4, pp. 300–305, 1985.

R. Akgedik, H. Karamanli, D. Kizilirmak et al., “Mounier-Kuhn syndrome (tracheobronchomegaly): An analysis of eleven cases,” The Clinical Respiratory Journal, vol. 12, no. 3, pp. 885–889, 2018.

E. N. Unlu, A. N. Annakkaya, E. G. Balbay et al., “An unusual cause of recurrent spontaneous pneumothorax: The Mounier-Kuhn syndrome,” The American Journal of Emergency Medicine, vol. 34, no. 1, pp. 122–122.e2, 2016.

A. Simkins, A. Maiti, S. V. Cherian, D. O. Trujillo, and R. M. Estrada-Y-Martin, “Mounier-Kuhn syndrome,” Postgraduate Medical Journal, vol. 93, no. 1104, pp. 642–642, 2017.