A 21-month-old boy was brought to the clinic by his mother for a hospital discharge follow-up visit. The patient had a history of gastroesophageal reflux disease, asthma attack, bronchiolitis, and recurrent wheezing. He had been admitted to the hospital for respiratory distress, tachypnea, and wheezing. He had required aggressive bronchodilation with intravenous corticosteroids. The patient also had had a hospital admission 5 month prior with a similar presentation.He had been born at 35 weeks of gestation via spontaneous vaginal delivery, and he had had a previous workup for aspiration (due to recurrent wheezing) at the age of 5 months that yielded positive bronchoalveolar lavage pepsin assay findings. His family history includes asthma in his brother, sister, mother, and paternal grandmother.Physical examination. At presentation, the patient was awake and alert, with no distress. Movement in all 4 extremities was even, with good strength. His temperature was 37.3 °C (temporal), his blood pressure was 115/66 mm Hg, his pulse rate was 102 beats/min, and his respiratory rate was 28 breaths/min. The patient's height was 84.4 cm (50th percentile) and his weight was 10.6 kg (25th percentile). The tympanic membranes appeared normal in both ears, the oropharynx was clear, and no discharge
Foresee Your Next PatientEndoscopic view of type 1 laryngeal cleft at presentation.