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1.
Journal of Breast Cancer ; : 286-296, 2017.
Artículo en Inglés | WPRIM | ID: wpr-83452

RESUMEN

PURPOSE: Accurate testing for estrogen receptor (ER), progesterone receptor (PR), and human epidermal growth factor receptor 2 (HER2) is essential for breast cancer treatment. At present, immunohistochemistry (IHC)/florescence in situ hybridization (FISH) are widely accepted as the standard testing methods. To investigate the value of NanoString nCounter®, we performed its comparative analysis with IHC/FISH and real-time quantitative reverse transcription polymerase chain reaction (qRT-PCR) for the assessment of ER, PR, and HER2. METHODS: Data on IHC/FISH results for ER, PR, and HER2 in 240 patients from a single tertiary hospital in Korea were collected and compared with NanoString nCounter® and qRT-PCR results at a single institution. RESULTS: Expression levels for each gene using NanoString nCounter® showed good correlation with the corresponding data for protein expression by IHC (p<0.001) and gene amplification status for HER2 (p<0.001). Comparisons between gene expression and IHC data showed good overall agreement with a high area under the curve (AUC) for ESR1/ER (AUC=0.939), PgR/PR (AUC=0.796), and HER2/HER2 (AUC=0.989) (p<0.001). CONCLUSION: The quantification of ER, PgR, and HER2 mRNA expression with NanoString nCounter® may be a viable alternative to conventional IHC/FISH methods.


Asunto(s)
Humanos , Neoplasias de la Mama , Mama , Estrógenos , Amplificación de Genes , Expresión Génica , Inmunohistoquímica , Hibridación in Situ , Corea (Geográfico) , Reacción en Cadena de la Polimerasa , Reacción en Cadena en Tiempo Real de la Polimerasa , Receptores ErbB , Receptores de Progesterona , Transcripción Reversa , ARN Mensajero , Centros de Atención Terciaria
2.
Korean Journal of Pathology ; : 314-317, 2006.
Artículo en Inglés | WPRIM | ID: wpr-204579

RESUMEN

Primary osteosarcoma of the skull is a rare finding. We report here on a pathologically proven case of osteosarcoma that presented as a painless mass in the frontal bone of a 7-year-old boy. This unusual form of osteosarcoma had features of desmoplastic fibroma in a large portion of the tumor. We also include a review of the medical literature related to osteosarcoma.


Asunto(s)
Niño , Humanos , Masculino , Fibroma Desmoplásico , Hueso Frontal , Osteosarcoma , Cráneo
3.
Korean Journal of Pathology ; : 269-272, 2005.
Artículo en Inglés | WPRIM | ID: wpr-202808

RESUMEN

Giant cell tumor of bone is a locally aggressive benign neoplasm, which is composed of oval or plump, spindle-shaped mononuclear cells and uniformly distributed multinucleated giant cells. Bone or cartilage matrix production by the tumor cells is usually not seen. We present a pathologically proven case of giant cell tumor, arising in the acetabulum and pubic bone, with unusual cartilage matrix production. We also discuss the differential diagnosis from a chondroblastoma as well as a giant cell-rich osteosarcoma.


Asunto(s)
Acetábulo , Cartílago , Condroblastoma , Diagnóstico Diferencial , Tumor Óseo de Células Gigantes , Tumores de Células Gigantes , Células Gigantes , Osteosarcoma , Hueso Púbico
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