Necrotizing Sarcoid Granulomatosis: A Disease Not to be Forgotten

Author:

Parejo-Morón A. I.1ORCID,Tornero-Divieso M. L.1,Férnandez-Díaz M. R.1,Muñoz-Medina L.2,Preda O.3,Ortego-Centeno N.456

Affiliation:

1. Servicio de Medicina Interna, Hospital Universitario Clínico San Cecilio, Granada, Spain

2. UGC Enfermedades Infecciosas, Hospital Universitario Clínico San Cecilio, Granada, Spain

3. Servicio de Anatomía Patológica, Hospital Universitario Clínico San Cecilio, Granada, Spain

4. Unidad de Enfermedades Autoinmunes Sistémicas, Hospital Universitario Clínico San Cecilio, Granada, Spain

5. Instituto Biosanitario Granada, Granada, Spain

6. Departamento de Medicina, Universidad de Granada, Granada, Spain

Abstract

Sarcoidosis 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). This is exactly what happened with the two cases that we present here.

Publisher

Hindawi Limited

Subject

General Medicine

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