| Literature DB >> 27606655 |
Tomás Díaz Angarita1, William Morales Camacho2, Laura Lozano Neira3, Jessica Plata Ortiz4, Linda Zárate Taborda3.
Abstract
Sarcoidosis is a granulomatous inflammatory disease of unknown etiology, evidenced most often in young adults, which can compromise several organs, mainly lung, lymph nodes, eyes and skin. The presence of the disease in pediatric population is rare. Denomination in pediatrics is made based on age and clinical manifestations of the patient. The aim of this report is to present a case of systemic sarcoidosis in a pediatric patient without lung involvement with severe extrapulmonary manifestations. Fifteen year old patient who debuted with nonspecific symptoms (emesis, weight loss). Radiographic studies without lung involvement but with findings suggestive of Langerhans cell histiocytosis; however, histopathological report (bone and lymph) showed the presence of chronic granulomatous nonnecrotizing disease, sarcoidosis type. Childhood sarcoidosis is a rare and difficult entity to diagnose, mainly by the lack of specific biomarkers for diagnosis. Sociedad Argentina de Pediatría.Entities:
Keywords: Child; Diagnosis; Pulmonary disease; Sarcoidosis
Mesh:
Year: 2016 PMID: 27606655 DOI: 10.5546/aap.2016.e323
Source DB: PubMed Journal: Arch Argent Pediatr ISSN: 0325-0075 Impact factor: 0.635