Purpose: Micropapillary bladder carcinoma is rare, with only 18 cases repor
ted to date. We report 20 additional cases with long-term followup.
Materials and Methods: A total of 680 patients with an initial diagnosis of
bladder carcinoma in western Sweden in 1987 and 1989 were prospectively re
gistered. The clinical records of all 816 patients with bladder cancer trea
ted at Sahlgrenska University Hospital with external beam irradiation betwe
en 1962 and 1989 were reviewed. The histopathological material was reviewed
and immunohistochemical analyses were performed on 20 cases identified wit
h micropapillary bladder carcinoma.
Results: The incidence of micropapillary bladder carcinoma was 0.7%. Mean p
atient age at diagnosis was 69 years (range 45 to 82) and the male-to-femal
e ratio was 2.3:1. All but 5 patients had stage T3a disease or higher. Ther
e was no difference in stage or prognosis between the 5 prospectively ident
ified patients and those treated with external beam irradiation. Only 2 pat
ients had micropapillary bladder carcinoma as the only pattern, while 1 had
10% and the remainder had 20 to 95% micropapillary bladder carcinoma. Tran
sitional cell carcinoma was noted in 17 patients and 5 had areas of gland f
orming adenocarcinoma. Carcinoma in situ was noted in 13 patients and 15 ha
d lymphatic invasion. Only 5 patients survived 5 years, 1 of whom died of b
ladder cancer after 7 years. Radiation and chemotherapy did not seem to be
effective.
Conclusions: The light microscopic appearance, which is strikingly similar
to ovarian papillary serous carcinoma, and immunohistochemical staining pat
tern lend some support to tale theory that micropapillary bladder carcinoma
is a variant of adenocarcinoma. Since even tale focal presence of micropap
illary bladder carcinoma is associated with a poor prognosis, recognition o
f this entity is important. Due to its rarity, the optimal treatment of mic
ropapillary bladder carcinoma needs to be determined in a multicenter study
.