COLLISION OF TRANSITIONAL-CELL CARCINOMA AND RENAL-CELL CARCINOMA - AN IMMUNOHISTOCHEMICAL STUDY AND REVIEW OF THE LITERATURE

Citation
Ap. Hart et al., COLLISION OF TRANSITIONAL-CELL CARCINOMA AND RENAL-CELL CARCINOMA - AN IMMUNOHISTOCHEMICAL STUDY AND REVIEW OF THE LITERATURE, Cancer, 73(1), 1994, pp. 154-159
Citations number
35
Categorie Soggetti
Oncology
Journal title
CancerACNP
ISSN journal
0008543X
Volume
73
Issue
1
Year of publication
1994
Pages
154 - 159
Database
ISI
SICI code
0008-543X(1994)73:1<154:COTCAR>2.0.ZU;2-G
Abstract
A case characterized by a rare synchronous occurrence of transitional cell carcinoma (TCC) of the renal pelvis and renal cell carcinoma (RCC ) in the same kidney is presented. A retrospective analysis of 23 simi lar cases reported in the English literature over the last 71 years de monstrated a male-to-female ratio of 2:1, an average age of 64.5 years , and a left-to-right-side ratio of 3.2:1. The three most common findi ngs at initial examination were hematuria (90%), flank pain (19%), and flank mass (14%). Moreover, 24% of patients had tumor metastases even at initial examination. Thirty-four percent of patients had bladder n eoplasms, and 24% of them had a history of cigarette smoking. There is no tendency toward higher grade of malignancy or specific histologic pattern for TCC and RCC when they occur together in the same kidney. I mmunohistochemical studies were used to examine TCC and RCC, with spec ial attention paid to the site of their collision, which displayed mul tifocal lymphatic permeation. Both TCC and RCC were positive for epith elial membrane antigen (EMA) and cytokeratins identified by monoclonal antibodies CAM-5.2, AE1/AE3, and MAK-6. TCC was focally positive for keratin, detectable by antibody 34 beta E12, but RCC was not. The tumo r tissue infiltrating the lymphatics, which seemed to be RCC, demonstr ated positive staining for EMA and keratins CAM-5.2, AE1/AE3, and MAK- B and negative staining for keratin 34 beta E12. Interestingly, the tu mor in lymphatics displayed strong staining for carcinoembryonic antig en (CEA) but both TCC and RCC in the vicinity were negative. These fin dings suggest that keratin 34 beta E12 may play a role in the differen tial diagnosis between TCC and RCC and that tumor-invading lymphatics may change phenotype, including the neoexpression of CEA.