Literature DB >> 27606655

[Systemic sarcoidosis: a diagnostic challenge in pediatrics. Case report].

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


  1 in total

1.  Hypercalcaemic Pancreatitis, Adrenal Insufficiency, Autoimmune Thyroiditis and Diabetes Mellitus in a girl with Probable Sarcoidosis.

Authors:  Devi Dayal; Olivia Pepper; Renuka Ramakrishnan; Eileen Baildam; Poonam Dharmaraj; Gavin Cleary; Liza McCann; Clare Pain; Senthil Senniappan
Journal:  Int J Endocrinol Metab       Date:  2017-08-22
  1 in total

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