A. Lopez-beltran et al., Lymphoepithelioma-like carcinoma of the urinary bladder: a clinicopathologic study of 13 cases, VIRCHOWS AR, 438(6), 2001, pp. 552-557
Citations number
18
Categorie Soggetti
Medical Research Diagnosis & Treatment
Journal title
VIRCHOWS ARCHIV-AN INTERNATIONAL JOURNAL OF PATHOLOGY
Lymphoepithelioma-like carcinoma (LELCA) of the urinary bladder is a rare v
ariant of bladder cancer characterized by a malignant epithelial component
densely infiltrated by lymphoid cells. It is characterized by indistinct cy
toplasmic borders and a syncytial growth pattern. These neoplasms deserve r
ecognition and attention. chiefly because they may be responsive to chemoth
erapy. We report on the clinicopathologic features of 13 cases of LELCA rec
orded since 1981. The chief complaint in all 13 patients was hematuria. The
ir ages ranged from 58 years to 82 years. All tumors were muscle invasive.
A significant lymphocytic reaction was present in all of these tumors. Ther
e were three pure LELCA and six predominant LELCA with a concurrent transit
ional cell carcinoma (TCC). The remainder four cases had a focal LELCA comp
onent admixed with TCC. Immunohistochemistry showed LELCA to be reactive ag
ainst epithelial membrane antigen and several cytokeratins (CKs; AE1/AE3, A
E1, AE3, CK7, and CK8). CK20 and CD44v6 stained focally. The lymphocytic co
mponent was composed of a mixture of T and B cells intermingled with some d
endritic cells and histiocytes. Latent membrane protein 1 (LMP1) immunostai
ning and in situ hybridization for Epstein-Barr virus were negative in all
13 cases. DNA ploidy of these tumors gave DNA histograms with diploid peaks
(n = 7) or non-diploid peaks (aneuploid or tetraploid; n = 6). All patient
s with pure and 66% with predominant LELCA were alive, while all patients h
aving focal LELCA died of disease. Our data suggest that pure and predomina
nt LELCA of the bladder appear to be morphologically and clinically differe
nt from other bladder (undifferentiated and poorly differentiated conventio
nal TCC) carcinomas and should be recognized as separate clinicopathologica
l variants of TCC with heavy lymphocytic reaction relevant in patient manag
ement.