Amylose systémique découverte par une atteinte trachéobronchique

Autor:	F. Nasr, G. Dabar, S. Mallat, Fady Haddad, M. Jammal, H. Azar, C. Ghorra
Rok vydání:	2010
Předmět:	Pathology medicine.medical_specialty AA amyloidosis Tracheobronchial amyloidosis business.industry Amyloidosis Gastroenterology Internal Medicine medicine medicine.disease business Systemic amyloidosis
Zdroj:	La Revue de Médecine Interne. 31:e4-e6
ISSN:	0248-8663
DOI:	10.1016/j.revmed.2009.03.353
Popis:	Amyloidosis is a spectrum of disease characterized by the abnormal deposition of fibril amyloid-related proteins in the extracellular space. The most common types of amyloidosis are AL and AA amyloidosis. Amyloidosis is also classified according to the extent of the deposition as systemic or localized. Respiratory amyloidosis is classified as laryngeal, tracheobronchial or parenchymal amyloidosis. Tracheobronchial amyloidosis is classically known as a rare manifestation of the localized disease. A few cases only of systemic amyloidosis presenting as a tracheobronchial disease have been reported. We here report a 26-year-old man who presented with hemoptysis related to a systemic tracheal primary amyloidosis.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::cb23c36a1fbe407acf69aa80db698ae0 https://doi.org/10.1016/j.revmed.2009.03.353 Zobrazit plný text záznamu Full Text from ScienceDirect