Objective: This rare bur aggressive bladder tumour presents the morphologic
al and immunohistochemical characteristic, common to all neuroendocrine tum
ours observed in other organs This study analyzed the diagnostic criteria a
nd therapeutic results obtained in 5 consecutive patients over a 3-year per
iod.
Materials and Methods: 5 patients (3 men and 2 women) suffering from primar
y small cell carcinoma of the bladder were evaluated. Histological diagnosi
s, treatment modalities and outcome were reviewed.
Results: The main clinical presentation was macroscopic haematuria. All tum
ours were invasive at the time of diagnosis 4 patients were treated by tran
s urethral resection alone, 2 of whom also received adjuvant radio- chemoth
erapy One patient was treated by radical cystectomy. The 4 patients treated
by conservative treatment modality had progression and a shorter survival,
in contrast with patient treated by radical cystectomy.
Conclusion: The urologist must recognize this rare histological entity whic
h have a poor prognosis and requires multidisciplinary management Treatment
must consist of a combination of neoadjuvant or adjuvant chemotherapy and
surgery to achieve the best results.