Plexiform Fibrohistiocytic Tumor of the Neck: A Case Report
Korean Journal of Pathology
;
: 211-213, 2005.
Artículo
en Inglés
| WPRIM
| ID: wpr-117903
ABSTRACT
Plexiform fibrohistiocytic tumor (PFT) is a rare, low-grade soft tissue tumor that occurrs primarily in children and young adults. The most common location of PFT is the upper extremity, and there are very few reports of PFT in the neck. We report here on a case of PFT presenting as a painless subcutaneous nodule in the neck of a 46-year-old woman. Histologically, this subcutaneous tumor was composed of a plexiform proliferation of histiocyte-like cells and fibroblast-like cells along with a few multinucleated osteoclast-like giant cells. Immunohistochemically, the tumor cells were positive for vimentin, CD68 and smooth muscle actin (SMA).
Texto completo:
Disponible
Índice:
WPRIM (Pacífico Occidental)
Asunto principal:
Vimentina
/
Células Gigantes
/
Actinas
/
Extremidad Superior
/
Músculo Liso
/
Cuello
Límite:
Niño
/
Femenino
/
Humanos
Idioma:
Inglés
Revista:
Korean Journal of Pathology
Año:
2005
Tipo del documento:
Artículo
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