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Tipos de Cancer / Cánceres de la Vía Urinaria / Cáncer Ureteral / Recursos de NCI
National Cancer Institute®
Ultima Vez Modificado: 1 de octubre del 2002
1
UI - 12201944
AU - Kupeli S; Yilmaz E; Atasoy P; Tulunay O
TI -
Prostatic urethral leukoplakia with prostatic abscess.
SO - Scand J Urol Nephrol 2002;36(3):234-5
AD - Department of Urology, School of Medicine, University of Ankara, Turkey.
We present a case of prostatic abscess and coexistent leukoplakia of the
urethra in a 51-year-old man. He had been suffering from diabetes
mellitus for 10 years and following cessation of high fewer,
transurethral electrovaporesection was performed.
2
UI - 12031867
AU - Tolley DA; Esposito MP
TI -
Laparoscopic and renal sparing approaches to tumours of the ureter and
kidney.
SO - Surg Oncol 2002 Jun;11(1-2):47-54
AD - Scottish Lithotriptor Centre, Western General Hospital, Edinburgh, UK.
datollet@baus.org.uk
Until recently, malignancies of the kidney and ureter were managed with
open radical surgery. Over the last decade the urologic community has
adopted the skill of laparoscopic surgery for the treatment of these
tumours. Parenchymal sparing procedures have become the standard of care
in the treatment of selected patients with renal and ureteral tumours
and many of these surgical procedures can be performed laparoscopically
or ureteroscopically. Due partly to necessity and partly to the
advancement of technology, renal and ureteral sparing procedures have
become commonplace for definitive treatment and palliation of these
tumours. The morbidity of such procedures is significantly less than for
open surgery and the future of urologic minimally invasive surgery
appears secure. This review article is aimed at updating the reader in
the most recent advances in these techniques.
3
UI - 12237912
AU - Ricci S; Galli L; Chioni A; Iannopollo M; Antonuzzo A; Francesca F;
TI -
Vocaturo V; Selli C; Orlandini C; Conte P
Gemcitabine plus epirubicin in patients with advanced urothelial
carcinoma who are not eligible for platinum-based regimens.
SO - Cancer 2002 Oct 1;95(7):1444-50
AD - Division of Medical Oncology, Department of Oncology, S. Chiara
University Hospital, Pisa, Italy. s.ricci@med.unipi.it
BACKGROUND: The objective of this study was to evaluate the efficacy and
toxicity of gemcitabine plus epirubicin in previously untreated patients
with advanced urothelial carcinoma who were not eligible for
cisplatin-based regimens. METHODS: Patients with advanced urothelial
carcinoma and at least one of the following characteristics were
eligible: impaired renal function (creatinine clearance < 60 mL per
minute), an Eastern Cooperative Oncology Group performance status (PS)
>or= 2, and age >or= 75 years. The treatment included epirubicin 70
mg/m(2) as an intravenous bolus on Day 1 and gemcitabine 1000 mg/m(2)
over 30 minutes on Days 1 and 8 of a 21-day cycle. RESULTS: Thirty-eight
patients entered the study, and a total of 152 cycles were administered,
with a median of 4 cycles per patient (range, 1-6 cycles per patient).
The following Grade 3-4 hematologic toxicities were reported (percent of
cycles): neutropenia, 22.4%; anemia, 11.2%; and thrombocytopenia, 6.5%.
No cardiac, renal, or hepatic toxicities were observed. Dose intensities
of epirubicin and gemcitabine were 19.6 mg/m(2) per week (84%) and 532.2
mg/m(2) per week (80%), respectively. There were 2 complete responses
(5.3%), 13 partial responses (34.2%), 11 patients with stable disease
(28.9%), and 12 patients with progressive disease (31.6%), for an
overall response rate of 39.5% (95% confidence interval, 25.1-55.1). The
median progression free survival (PFS) and overall survival (OS) rates
were 4.8 months and 8.0 months, respectively. The 1-year survival rate
was 38%, and the median PFS and OS were 6.4 months and 16.4 months,
respectively, in patients with PS 0-1. Thirty patients were symptomatic:
Seventeen patients (56.7%) achieved a complete response, and 5 patients
(16.7%) achieved a partial symptomatic response. CONCLUSIONS: At the
doses given in this study, gemcitabine and epirubicin had a good
tolerability profile with interesting activity in patients with advanced
urothelial carcinoma who were not fit for cisplatin-based regimens.
Copyright 2002 American Cancer Society.DOI 10.1002/cncr.10860
4
UI - 12352398
AU - Thalmann GN; Markwalder R; Walter B; Studer UE
TI -
Long-term experience with bacillus Calmette-Guerin therapy of upper
urinary tract transitional cell carcinoma in patients not eligible for
surgery.
SO - J Urol 2002 Oct;168(4 Pt 1):1381-5
AD - Department of Urology, University of Bern, Switzerland.
PURPOSE: Carcinoma in situ and urothelial tumors of the upper urinary
tract become problematic in cases of bilateral occurrence or solitary
kidney. Perfusions with bacillus Calmette-Guerin (BCG) have been
reported beneficial, however, only long-term results will determine the
validity of this treatment. MATERIALS AND METHODS: We retrospectively
evaluated the results of BCG therapy for upper urinary tract disease in
37 patients. All 37 patients had undergone previous surgical treatment
for urothelial cancer, had a positive cytology or biopsy for upper
urinary tract cancer and were ineligible for radical nephroureterectomy
with a bladder cuff. After placement of a 10Fr nephrostomy tube with the
patient under local anesthesia 6 weekly perfusions of BCG were
administered after radiological documentation of unhindered flow from
the renal pelvis to the bladder or urinary diversion. A total of 25
renal units were treated with curative intent for carcinoma in situ and
16 renal units were treated for Ta or higher urothelial tumors in an
adjuvant setting after endoscopic resection. RESULTS: In 37 patients 41
renal units were treated with BCG perfusions and were followed for a
median of 42 months (range 8 to 137). In 1 patient BCG inflammation and
in 2 others severe septicemia developed after the first perfusion. There
was no tumor seeding along the nephrostomy tract in any patient. BCG
perfusion therapy did not alter renal function. Overall median survival
was 42 months (range 1 to 137), median recurrence-free survival was 21
months (1 to 137) and progression-free survival was 34 months (1 to
118). Of the 37 patients 14 (38%) died of urothelial cancer, 11 of other
causes (29%) and 12 (33%) are alive. CONCLUSIONS: BCG perfusion therapy
of the upper urinary tract for papillary tumors or carcinoma in situ is
a valid treatment option with acceptable side effects for patients not
amenable to conventional radical surgical therapy. BCG therapy of upper
urinary tract urothelial tumors may prevent patients from requiring
dialysis and provides cure in those with carcinoma in situ of the upper
urinary tract. In this negatively selected patient population BCG buys
time for some but does not provide cure except for carcinoma in situ.
5
UI - 12002603
AU - Hara M; Satake M; Ogino H; Itoh M; Miyagawa H; Hashimoto Y; Okabe M;
TI -
Inagaki H
Primary ureteral mucosa-associated lymphoid tissue (MALT)
lymphoma--pathological and radiological findings.
SO - Radiat Med 2002 Jan-Feb;20(1):41-4
AD - Department of Radiology, Nagoya City University Medical School,
Kawasumi, Japan.
In this report we describe the pathological and radiological findings in
a patient with primary ureteral MALT lymphoma. We suggest that it is
useful for the differential diagnosis of ureter masses that some MALT
lymphomas may show a low signal intensity on T2-weighted MR images.
6
UI - 11952296
AU - Karthikeyan K; Kaviarasan PK; Thappa DM
TI -
Urethral caruncle in a male: a case report.
SO - J Eur Acad Dermatol Venereol 2002 Jan;16(1):72-3
AD - Department of Dermatology and STD, Jawaharlal Institute of Postgraduate
Medical Education and Research (JIPMER), Pondicherry, India.
Urethral caruncle in a 60-year-old male labourer is being reported. Its
occurrence in male urethra has not been reported so far in the
literature.
7
UI - 11147749
AU - Terzic MM; Stimec BV
TI -
A long-term course of a primary urethral/paraurethral adenocarcinoma.
SO - Int Urogynecol J Pelvic Floor Dysfunct 2000 Dec;11(6):392-4
AD - Department of Obstetrics and Gynecology, School of Medicine, Belgrade
University, Yugoslavia. milanter@EUnet.yu
The authors report a rare case of primary urethral/paraurethral
adenocarcinoma in a female patient. The tumor was first detected at the
external and internal urethral orifices, with later recurrences in the
region of the urinary bladder neck. Histology did not reveal the exact
origin of the malignancy. The patient was treated by transurethral
resection, regularly repeated during the 3-6-monthly checks. Five years
after diagnosis she remains symptom free and has a high quality of life.
8
UI - 11250797
AU - Mi ZG; Yang XF; Liang XZ; Liu HY; Liu SY; Zhang H; Wang DW; Liu C
TI -
Adenoma of the posterior urethra: 131 case report.
SO - Asian J Androl 2001 Mar;3(1):67-70
AD - Department of Urology, The First Affiliated Hospital, Shanxi Medical
University, Taiyuan, China.
AIM: A case-report on adenoma of the posterior urethra. METHODS: In 131
cases of adenoma of the posterior urethra, aged 17-79 (mean: 36.4)
years, a detailed medical history was taken and urinalysis,
urethroscopy, and prostatic specific antigen (PSA) immunohistochemical
staining were performed. They were then treated with transurethral
resection (TUR) or transurethral electric coagulation (TUEC). RESULTS:
Hemospermia occurred in 51% of the cases, hematuria in 38%, blood
overflow from the urethral orifice in 6%, and dysuria in 5%. The
position of the tumor was at or around the verumontanum. The appearance
of the tumor was similar to those of a papilla, a villus, a dactyl or
polyp, or simply an engorgement. The tumor contained glandular alveoli
and adeno-epithelial cells. PSA immunohistochemistry was positive in the
cytoplasm and nucleus of the adeno-epithelial cell. One hundred and
tweenty-nine cases were cured after TUR or TUEC, while 2 patients
recurred and were operated again. CONCLUSION: Adenoma of the posterior
urethra is a common cause of hemospermia and hematuria in young men.
Urethroscopic examination and biopsy are the principal diagnostic
measures. TUR or TUEC are believed to be the treatment of choice with a
short-term recurrence rate of around 1. 5%.
The above citations and abstracts reflect those newly added to CANCERLIT for the month and topic listed in the title. The citations have been retrieved from CANCERLIT using a predefined search strategy of indexed subject terms. Although the search strategy has been refined as best as possible, citations may appear that are not directly related to the topic, and occasionally relevant references may be omitted.
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