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
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.