Àá½Ã¸¸ ±â´Ù·Á ÁÖ¼¼¿ä. ·ÎµùÁßÀÔ´Ï´Ù.

Rhabdoid Colorectal Carcinomas: Reports of Two Cases

´ëÇѺ´¸®ÇÐȸÁö 2013³â 47±Ç 4È£ p.372 ~ 377
ÀÌ»óÈ­, ¼³Çý½Ç, ±è¿í¿¬, ÀÓ¼Ò´ö, ±è¿Ï¼·, Ȳż÷, ÇÑÇý½Â,
¼Ò¼Ó »ó¼¼Á¤º¸
ÀÌ»óÈ­ ( Lee Sang-Hwa ) 
Aerospace Medical Center Research Center Department of Pathology

¼³Çý½Ç ( Seol Hye-Sil ) 
Konkuk University School of Medicine Department of Pathology
±è¿í¿¬ ( Kim Wook-Youn ) 
Konkuk University School of Medicine Department of Pathology
ÀÓ¼Ò´ö ( Lim So-Dug ) 
Konkuk University School of Medicine Department of Pathology
±è¿Ï¼· ( Kim Wan-Seop ) 
Konkuk University School of Medicine Department of Pathology
Ȳż÷ ( Hwang Tae-Sook ) 
Konkuk University School of Medicine Department of Pathology
ÇÑÇý½Â ( Han Hye-Seung ) 
Konkuk University School of Medicine Department of Pathology

Abstract


Rhabdoid colorectal carcinomas are very rare and only 10 cases have been previously reported. We report two cases of rhabdoid colorectal carcinoma, one arising in the sigmoid colon of a 62-year-old man and another in the rectum of an 83-year-old woman. In both cases, the patients had advanced tumors with lymph node metastases. The tumors mostly showed a diffuse arrangement with rhabdoid features and small glandular regions were combined. Transitional areas from the adenocarcinomas to the rhabdoid tumors were also noted. Adenocarcinoma cells were positive for mixed cytokeratin (CK), CK20 and epithelial membranous antigen (EMA), but focal positive for vimentin. The rhabdoid tumor cells were positive for mixed CK, but focal positive or negative for CK20 and EMA. In addition, they were diffusely positive for vimentin, but negative for desmin. The histological and immunohistologial findings of these two cases suggest that the rhabodid tumor cells originated from dedifferentiated adenocarcinomas.

Å°¿öµå

Adenocarcinoma; Colon; Rectum; Rhabdoid tumor

¿ø¹® ¹× ¸µÅ©¾Æ¿ô Á¤º¸

  

µîÀçÀú³Î Á¤º¸

KCI
KoreaMed
KAMS