Histiocitosis de células de langerhans. Un hallazgo poco común en la glándula tiroides. A propósito de un caso

Autores/as

DOI:

https://doi.org/10.53732/rccsalud/03.02.2021.102

Palabras clave:

histiocitosis de células de langerhans, tiroides, neoplasia

Resumen

La histiocitosis de células de Langerhans (HCL) es una neoplasia mieloide, poco común, se caracteriza por la proliferación de células histiocíticas CD1a+/Langerina+. La incidencia en adultos es 1 a 2 casos por millón, un poco más frecuente en niños. La presentación es variable, como una única lesión en un órgano hasta una enfermedad multisistémica con toque de órganos vitales. Los tejidos de mayor afinidad son: huesos, piel, pulmones e hipófisis y raramente tiroides. El retraso en el diagnóstico o en el tratamiento puede provocar un deterioro de la función de los órganos afectados. El objetivo de la comunicación es reportar un caso de HCL, de presentación aún menos frecuente, en forma aislada en la glándula tiroides de un adulto, hallazgo hecho tras una tiroidectomía total, realizándose el diagnóstico luego de la histología.

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Publicado

2021-11-20

Cómo citar

López H, H., Galeano S, S., Ferreira, D., Romero F, F., Salinas V, V., Lezcano H, H., Rodriguez, I., & Valinotti, E. (2021). Histiocitosis de células de langerhans. Un hallazgo poco común en la glándula tiroides. A propósito de un caso. Revista científica Ciencias De La Salud - ISSN: 2664-2891, 3(2), 102–111. https://doi.org/10.53732/rccsalud/03.02.2021.102