Juvenile-onset recurrent respiratory papillomatosis with pulmonary involvement and carcinomatous transformation
Papilloma associated with recurrent respiratory papillomatosis (RRP), caused by human papilloma virus (HPV) infection types 6 and 11, is the most common benign neoplasm of the larynx. The clinical features of RRP vary widely from mild to aggressive forms. RRP in children is known as juvenile-onset r...
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Published in: | Autopsy & case reports Vol. 8; no. 3; p. e2018035 |
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Main Authors: | , , , , , |
Format: | Journal Article |
Language: | English |
Published: |
Brazil
São Paulo, SP: Universidade de São Paulo, Hospital Universitário
01-08-2018
University of São Paulo |
Subjects: | |
Online Access: | Get full text |
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Summary: | Papilloma associated with recurrent respiratory papillomatosis (RRP), caused by human papilloma virus (HPV) infection types 6 and 11, is the most common benign neoplasm of the larynx. The clinical features of RRP vary widely from mild to aggressive forms. RRP in children is known as juvenile-onset recurrent respiratory papillomatosis (JORRP). Its outcome may be poor or even fatal due to the high rate of recurrence and eventual spread to the entire respiratory tract. Pulmonary invasion is reported to occur in 3.3% of patients with RRP, and malignant transformation in 0.5% of patients. We report the case of a 39-year-old female patient with a diagnosis of JORRP from the age of 3 years, with extensive bilateral pulmonary involvement and malignant transformation. Analysis of the papilloma and carcinomatous tissues revealed the presence of HPV type 11, which is associated with rapid and aggressive progression. We discussed the case on the basis of a literature review on pulmonary invasion, malignant transformation, and HPV 11 aggressiveness. |
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Bibliography: | Conflict of interest: None Authors contributions: All of the authors participated in the conception of this study, in the analysis and interpretation of the results, and in the elaboration and critical review of the final manuscript. |
ISSN: | 2236-1960 2236-1960 |
DOI: | 10.4322/acr.2018.035 |