A Case of Langerhans Cell Histiocytosis Involving the Thyroid Gland: Ultrasonographic Finding
Journal of the Korean Society of Medical Ultrasound
; : 67-70, 2013.
Article
Dans Ko
| WPRIM
| ID: wpr-725547
Responsable en Bibliothèque :
WPRO
ABSTRACT
Langerhans cell histiocytosis is a rare, proliferative monoclonal histiocytic disease of unknown cause. Primary involvement of the thyroid gland by LCH is very rare, and most cases show evidence of LCH involving other organs. Herein, we report on a case of thyroid LCH in a patient diagnosed as pituitary gland LCH. When a patient with a history of LCH presents with enlargement of the thyroid gland or a neck mass, and ultrasonography shows a well-defined low echoic mass, LCH should be included in differential diagnosis. Fine needle aspiration can be useful for initial diagnosis; however, for differentiation with thyroiditis or thyroid cancer, core biopsy, positive S-100 protein, and CD1a immunohistochemical staining are needed.
Texte intégral:
1
Indice:
WPRIM
Sujet Principal:
Hypophyse
/
Glande thyroide
/
Thyroïdite
/
Biopsie
/
Tumeurs de la thyroïde
/
Protéines S100
/
Histiocytose à cellules de Langerhans
/
Cytoponction
/
Diagnostic différentiel
/
Cou
Type d'étude:
Diagnostic_studies
Limites du sujet:
Humans
langue:
Ko
Texte intégral:
Journal of the Korean Society of Medical Ultrasound
Année:
2013
Type:
Article