Spontaneous pneumothorax as a clinical manifestation of neurofibromatosis type 1

Neurofibromatosis type 1 (NF1) is a genetic disorder affecting the skin, nervous system, eyes and bones. Pulmonary involvement is unknown to many physicians. Yet, patients may be affected by lung bullae and cysts, which represent an increased risk for secondary spontaneous pneumothorax (SSP). We pre...

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Detalles Bibliográficos
Autores principales: Lorentzen, Tine, Madsen, Hanne, Lausten-Thomsen, Marie Josée Zareh, Bygum, Anette
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7978331/
https://www.ncbi.nlm.nih.gov/pubmed/33737277
http://dx.doi.org/10.1136/bcr-2020-238694

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7978331/
https://www.ncbi.nlm.nih.gov/pubmed/33737277
http://dx.doi.org/10.1136/bcr-2020-238694

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