Langerhans Cell Histiocytosis of the Clavicle in a 50-Year-Old Male: A Case Report
Journal of the Korean Radiological Society
; : 936-942, 2021.
Article
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| WPRIM
| ID: wpr-901311
Biblioteca responsable:
WPRO
ABSTRACT
Langerhans cell histiocytosis (LCH) is a rare condition that usually occurs in children and commonly affects the skeletal system. It is extremely rare in adults, especially in the clavicles. In this report, we describe a pathologically confirmed case of LCH in the clavicle of a 50-year-old male. We report various radiological findings, such as plain radiography, CT, MR, and PET-CT, along with a review of the literature.
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Base de datos:
WPRIM
Idioma:
En
Revista:
Journal of the Korean Radiological Society
Año:
2021
Tipo del documento:
Article