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Lymphoepithelioma-like Carcinoma of the Renal Pelvis: A Case Report and Review of the Literature

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¾ÈÇýÀÎ, ½ÉÁ¾¹Î, ±èÇö¼º, Yi Ki-Jong, Han Hulin, Á¤À¯¹Î, Rehman Abdul, ¹é½Â»ï,
¼Ò¼Ó »ó¼¼Á¤º¸
¾ÈÇýÀΠ( Ahn Hye-In ) 
Hanyang University College of Medicine Department of Pathology

½ÉÁ¾¹Î ( Sim Jong-Min ) 
Hanyang University College of Medicine Department of Pathology
±èÇö¼º ( Kim Hyun-Sung ) 
Hanyang University College of Medicine Department of Pathology
 ( Yi Ki-Jong ) 
Hanyang University College of Medicine Department of Pathology
 ( Han Hulin ) 
Hanyang University College of Medicine Department of Pathology
Á¤À¯¹Î ( Chung Yu-Min ) 
Hanyang University College of Medicine Department of Pathology
 ( Rehman Abdul ) 
Hanyang University College of Medicine Department of Pathology
¹é½Â»ï ( Paik Seung-Sam ) 
Hanyang University College of Medicine Department of Pathology

Abstract


Lymphoepithelioma is an undifferentiated epithelial tumor primarily described in the nasopharynx and characterized by
syncytial nests of malignant epithelial cells with a prominent reactive lymphoid infiltrate.1 A carcinoma that shows similar
histological features but arises outside the nasopharynx is called lymphoepithelioma-like carcinoma (LELC). LELC has been described in a variety of organs including salivary glands, thymus, lungs, stomach, skin, uterine cervix, breast, prostate, and the urinary tract.2 The renal pelvis is an extremely rare site for this tumor. To the best of our knowledge, only eight cases have been reported in the English literature and one case has been reported in the Korean literature.1-8 We recently experienced a case of LELC arising in the right renal pelvis in a 65-year-old woman.

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