bronchomalacia/mæði

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[A case of Saber-sheath type tracheo-bronchomalacia].

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A case of Saber-sheath type tracheo-bronchomalacia complicating bronchial asthma was treated by external fixation of Marlex mesh, and good results were obtained. The patient was a 43-year-old male who had been treated for bronchial asthma for over nearly 20 years. Since 4 years ago, dyspnea and a

[Use of a laryngeal mask airway for anesthesia in a patient with bronchomalacia].

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A 56-year-old woman with bronchomalacia underwent three consecutive operations for bronchoscopy, cautery YAG-laser, and the insertion of a stent under general anesthesia using a laryngeal mask airway (LMA). For the first operation, anesthesia was induced with ketamine 20 mg, diazepam 5 mg and

An unusual cause of breathlessness after lobectomy for lung cancer.

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Localized bronchomalacia as a cause of breathlessness after lobectomy is an unusual complication. This condition was diagnosed with bronchoscopy and delineated by spiral computed tomographic scan. Stenting the lesion resulted in a successful outcome.

Pseudo-asthma: when cough, wheezing, and dyspnea are not asthma.

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Although asthma is the most common cause of cough, wheeze, and dyspnea in children and adults, asthma is often attributed inappropriately to symptoms from other causes. Cough that is misdiagnosed as asthma can occur with pertussis, cystic fibrosis, primary ciliary dyskinesia, airway abnormalities

Endobronchial stent placement for the management of airway complications after lung transplantation.

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OBJECTIVE To retrospectively evaluate the efficacy and complications of endobronchial stent placement for the management of airway complications following lung transplant. METHODS From 1992 to 2003, tracheobronchial stenting was performed on 25 lung transplant recipients (16 male and 9 female; mean

Successful reconstruction of communicating bronchopulmonary foregut malformation associated with laryngotracheoesophageal cleft.

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A full-term newborn male infant presented with dyspnea and cleft lip and palate. He was thought to have esophageal atresia with tracheoesophageal fistula. He underwent bronchoscopy before operation that showed a laryngotracheoesophageal cleft (LTEC) type III. The left main bronchus originated from

Balloon dilation and endobronchial stent placement for bronchial strictures after lung transplantation.

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OBJECTIVE To evaluate the effect of balloon dilation and endobronchial stent placement for bronchial fibrous stenoses and bronchomalacia after lung transplantation. METHODS Bronchial dilation and/or stent placement was performed on 25 lung transplant recipients. Indications included severe dyspnea

Williams-Campbell syndrome: a case report.

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BACKGROUND Williams-Campbell syndrome, also known as bronchomalacia, is a rare disorder characterized by a deficiency of cartilage in subsegmental bronchi, leading to distal airway collapse and bronchiectasis. There have been few reports about patients affected by saccular bronchiectasis,

Laryngo-tracheo-oesophageal clefts.

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A laryngo-tracheo-esophageal cleft (LC) is a congenital malformation characterized by an abnormal, posterior, sagittal communication between the larynx and the pharynx, possibly extending downward between the trachea and the esophagus. The estimated annual incidence of LC is 1/10,000 to 1/20,000

Recovery of lung perfusion after sleeve resection for tuberculous bronchial stenosis.

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Parenchyma-sparing main bronchial sleeve resection is a safe and effective procedure to restore impaired lung function. We present a case illustrating recovery of lung perfusion in a 24-year-old woman with dyspnea on exertion because of bronchial tuberculosis. Bronchoscopic examination revealed

Central Airway Collapse, an Underappreciated Cause of Respiratory Morbidity

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Dyspnea, cough, sputum production, and recurrent respiratory infections are frequently encountered clinical concerns leading patients to seek medical care. It is not unusual for a well-defined etiology to remain elusive or for the therapeutics of a presumed etiology to be incompletely effective.

[Analysis of 53 cases with bronchoscopically confirmed pediatric tracheobronchomalacia].

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OBJECTIVE Tracheobronchomalacia is one of the common respiratory tract dysplasia in children. Its symptoms are nonspecific, and routine methods are unreliable in the assessment of tracheobronchomalacia in children. In addition, many physicians are confused about its clinical characteristics, so

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