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2.
Arch Esp Urol ; 73(9): 862-863, 2020 Nov.
Artigo em Inglês, Espanhol | MEDLINE | ID: mdl-33144543

RESUMO

A 62 year old man with a history of weight loss and left flank pain did a renal ultrasound that showed a heterogeneous formation involving the left kidney compatible with a solid lesion...


A un hombre de 62 años de edad con una historia de pérdida de peso y dolor en la region lombar izquierda, se le hizo un ultrasonido renal, que mostró una formación heterogénea en el riñón izquierdo compatible con una lesión sólida...


Assuntos
Nefropatias , Neoplasias Renais , Lipomatose , Humanos , Rim/diagnóstico por imagem , Nefropatias/diagnóstico por imagem , Nefropatias/etiologia , Neoplasias Renais/diagnóstico por imagem , Neoplasias Renais/cirurgia , Lipomatose/diagnóstico por imagem , Masculino , Pessoa de Meia-Idade , Ultrassonografia
4.
Urol Case Rep ; 11: 30-32, 2017 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-28083483

RESUMO

Paratesticular sarcomas are rare. Most cases reported in the literature are depending on retrospective analysis of case reports, small series, literature reviews, and expert opinion and they show different outcomes depending on several variables. The majority indicate that this may be an indolent tumor with a potential for cure if treated early. We present a case of a 58 year old man with a history of painless enlargement of the right testis. The ultrasound showed an extratesticular lesion and a right excisional of the mass was performed. The pathological examination revealed a leiomyosarcoma, and was then completed with a right radical inguinal orchiectomy. A review of the literature regarding paratesticular sarcomas presentation, diagnosis and treatment is presented in this article.

5.
Clin Genitourin Cancer ; 15(1): 117-121, 2017 02.
Artigo em Inglês | MEDLINE | ID: mdl-27436153

RESUMO

BACKGROUND: We evaluated whether the Vienna nomogram increases the detection rate of transrectal ultrasound-guided prostate biopsy compared with a 10-core biopsy protocol. PATIENTS AND METHODS: In the present prospective randomized study, men eligible for prostate biopsy were randomized to a Vienna nomogram protocol (group A) or a 10-core protocol (group B). They were further stratified according to age (≤ 65, > 65 but ≤ 70, and > 70 years) and prostate volume (≤ 30, > 30 but ≤ 50, > 50 but ≤ 70, and > 70 cm3). The cancer detection rate (CDR) was compared between the groups by logistic regression analysis, with adjustment for age as necessary, overall and with age and prostate volume stratification. Additional statistical analysis was performed with Fisher's exact test for contingency tables and the Mann-Whitney U test for 2 independent samples. P < .05 was considered statistically significant. A subgroup analysis was performed for patients with serum prostate-specific antigen levels of 2 to 10 ng/mL. RESULTS: From January 2009 to July 2010, 456 patients were enrolled, 237 to the Vienna nomogram group and 219 to the 10-core group. No significant differences were found in serum prostate-specific antigen or prostate volume between the 2 groups. Multivariate analysis with adjustment for age revealed no significant differences in CDR, with 42.6% in group A and 38.4% in group B (P = .705). When stratified by age and prostate volume, no statistically significant differences were found in the CDR between the groups in all subclasses. Also, in the subgroup analysis, CDR was not significantly different, 37.9% versus 34.7% for groups A and B, respectively (P = .891). CONCLUSION: These results study suggest that the use of the Vienna nomogram does not significantly increase the overall CDR compared with a 10-core biopsy scheme. Further prospective randomized studies, with adequate sample sizes, are needed to definitively determine the best prostate biopsy protocol.


Assuntos
Nomogramas , Neoplasias da Próstata/patologia , Idoso , Biópsia com Agulha de Grande Calibre , Humanos , Calicreínas/sangue , Masculino , Pessoa de Meia-Idade , Estudos Prospectivos , Antígeno Prostático Específico/sangue , Neoplasias da Próstata/sangue , Distribuição Aleatória , Sensibilidade e Especificidade
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