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Histiocitosis de células de Langerhans: reporte de caso y revisión de la literatura
Author(s) -
Miguel Ángel Medina,
Wendy Meyer,
Carolina Echeverri,
Natalia Builes
Publication year - 2021
Publication title -
biomédica/biomedica
Language(s) - Spanish
Resource type - Journals
SCImago Journal Rank - 0.26
H-Index - 28
eISSN - 2590-7379
pISSN - 0120-4157
DOI - 10.7705/biomedica.5430
Subject(s) - langerhans cell histiocytosis , medicine , humanities , pathology , disease , philosophy
Histiocytosis comprises a heterogeneous group of inflammatory diseases whose main cellular components are dendritic cells and macrophages. The inflammatory infiltrate can affect the skin and other organs and the clinical outcome varies from mild to fatal depending on the involved cell subset and multisystemic compromise. Delay in diagnosis may occur due to its non-specific presentation and to a low suspicion on the part of the clinician. We report the case of an infant who despite multiple consultations with nonspecific but characteristic symptoms of the disease was only finally diagnosed thanks to histopathological findings.

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