International Medical Case Reports Journal (Nov 2022)

Tracheobronchomegaly (Mounier-Kuhn Syndrome) in a 43-Year-Old Male: A Case Report

  • Babirye D,
  • Walubembe J,
  • Babirye JA,
  • Baluku JB,
  • Byakika-Kibwika P,
  • Nabawanuka E

Journal volume & issue
Vol. Volume 15
pp. 631 – 637

Abstract

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Deborah Babirye,1 Jonathan Walubembe,1 Juliet Allen Babirye,2 Joseph Baruch Baluku,2,3 Pauline Byakika-Kibwika,4 Eva Nabawanuka1 1Department of Radiology, Makerere University College of Health Sciences, Kampala, Uganda; 2Department of Research, Makerere University Lung Institute, Kampala, Uganda; 3Division of Pulmonology, Kiruddu National Referral Hospital, Kampala, Uganda; 4Department of Medicine, Makerere University College of Health Sciences, Kampala, UgandaCorrespondence: Deborah Babirye, Department of Radiology, Makerere University College of Health Sciences, PO Box 7072, Kampala, Uganda, Email [email protected]: Mounier-Kuhn syndrome (MKS) or congenital tracheobronchomegaly is a rare disorder characterized by marked dilatation of the trachea and main bronchi, bronchiectasis, and recurrent respiratory tract infections. The etiology of this disorder is uncertain and the clinical presentation is variable. The diagnosis is usually made based on the characteristic computed tomography (CT) scan findings. This report describes a case of a 43-year-old man presenting with persistent cough and recurrent lower respiratory tract infections since childhood associated with copious amounts of purulent sputum, difficulty in breathing, and weight loss. In addition, he reported palpitations, dyspnea, orthopnea, abdominal and lower limb swelling. The chest X-ray showed a dilated trachea (35mm) and bronchi (26mm (right) and 27mm (left)) with cystic bronchiectasis and reticulolinear opacities predominantly involving the middle and lower lung zones. Chest CT scan confirmed the diagnosis of MKS as evidenced by dilated trachea and bronchi complicated by diverticula formation. Electrocardiogram, echocardiography and abdominal ultrasound scan showed features of right-sided heart failure secondary to pulmonary hypertension. MKS, although rare, should be considered as a possible diagnosis in patients presenting with productive chronic cough, recurrent pneumonia, or incomplete response to appropriate antibiotic therapy for pneumonia.Keywords: Mounier-Kuhn syndrome, tracheobronchomegaly, MKS

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