Presentation
Symptoms of dyspnoea, dysphonia, hoarseness, increased vocal effort, noisy sleeping, dysphagia with solids, odynophagia.
Patient Data

Multiple nodules 5 mm or less are seen at the right anterolateral false cord, left posterolateral false cord, and the right anterolateral true cord.
Multiple tracheal nodules; one lesion along the left anterolateral trachea, another is a broad-based nodule seen along the left lateral tracheal wall, partially obscured by streak artifact from contrast bolus.

Protruding lesions along the tracheal wall in keeping with recurrent tracheal papillomatosis.
A cavitary lesion with internal septations in the right upper lobe increased in size compared to prior imaging from several years earlier (not shown).
A new pulmonary nodule was seen in the left upper lobe abutting the left major fissure—stable nodule in the right upper lobe.
Case Discussion
This patient has a long history of recurrent respiratory papillomatosis (RRP), starting at age 7. She presented for this imaging study after experiencing shortness of breath, dysphonia, dysphagia, increased vocal effort and voice changes, which are commonly associated symptoms of respiratory papillomatosis. Imaging demonstrates multiple papillomatous nodules throughout the upper airway, as well as a new cavitary lung lesion, which can be an associated feature.
Patient diagnosis is consistently confirmed by pathology of lesional biopsies demonstrating squamous papilloma with HPV cytopathic effect and low-grade dysplasia, and on staining is noted to have patchy p16 positivity and slightly elevated Ki-67 index. Due to juvenile onset, the patient had yet to receive HPV vaccination, but other risk factors related to vertical transmission were not available in the chart.
This patient underwent more than 100 excision procedures previously using carbon dioxide laser, potassium titanyl phosphate (KTP) laser, and microdebridement. For the last few years, adjunctive treatment with local injection of bevacizumab seemed to decrease the frequency of procedures from once every few weeks to 2 to 3 times per year. As symptoms continued to progress, the patient recently opted to undergo systemic treatment with a series of bevacizumab infusions. This imaging was obtained as a baseline before beginning infusions.
With regular treatment, as with this patient, RRP can be manageable. In severe cases and untreated patients, airway obstruction can occur and may require undergoing a tracheotomy. Patients like this one who had juvenile-onset RRP have a <1% chance of malignant transformation, but regular cytopathology is recommended.
Case co-authors:
Dr. Lara Aboud Syriani, Temple University Hospital, USA
Dr. Bhishak Kamat, Temple University Hospital, USA