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dc.contributor.authorParejo Morón, A. I.
dc.contributor.authorTornero Divieso, M. L.
dc.contributor.authorFernández Díaz, M. R.
dc.contributor.authorMuñoz Medina, Leopoldo
dc.contributor.authorPreda, O.
dc.contributor.authorOrtego Centeno, Norberto 
dc.date.accessioned2020-03-12T12:48:35Z
dc.date.available2020-03-12T12:48:35Z
dc.date.issued2020-01-28
dc.identifier.citationParejo-Morón, A. I., Tornero-Divieso, M. L., Férnandez-Díaz, M. R., Muñoz-Medina, L., Preda, O., & Ortego-Centeno, N. (2020). Necrotizing Sarcoid Granulomatosis: A Disease Not to be Forgotten. Case Reports in Medicine, 2020.es_ES
dc.identifier.urihttp://hdl.handle.net/10481/60229
dc.description.abstractSarcoidosis is a systemic granulomatous disease of unknown aetiology characterised by the appearance of noncaseifying epithelioid granulomas in the affected organs, most commonly the lungs, skin, and eyes (Iannuzzi et al. 2007). Necrotizing Sarcoid Granulomatosis (NGS) is a rare and little-known form of disease, which also presents nodular lung lesions, and it shares pathologic and clinical findings with sarcoidosis, where the presence of necrosis may lead to misdiagnosis of tuberculosis (TB), leading to a consequent delay in treatment of the underlying entity (Chong et al. 2015). ,is is exactly what happened with the two cases that we present here.es_ES
dc.language.isoenges_ES
dc.publisherHindawies_ES
dc.rightsAtribución 3.0 España*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.titleNecrotizing Sarcoid Granulomatosis: A Disease Not to be Forgottenes_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses_ES
dc.identifier.doi10.1155/2020/5730704


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Atribución 3.0 España
Except where otherwise noted, this item's license is described as Atribución 3.0 España