RESUMO
Introdução: O melanoma é essencialmente cutâneo. Em alguns pacientes, não é possível determinar a localização do tumor primário. A incidência de melanoma com sítio primário desconhecido varia de 2 a 15%. Objetivos: Determinar se há diferença de sobrevida global entre os pacientes com melanoma primário conhecido comparado aos pacientes com melanoma primário desconhecido. Métodos: Foi realizada análise retrospectiva de pacientes com melanoma no banco de dados da Oncologia Cirúrgica e Cirurgia do Aparelho Digestivo (ONCAD) e identificados aqueles com sítio primário desconhecido e metástases para diferentes locais. Resultados: O principal local de metástases foi o linfonodo (50%) - inguinais (25%),axilares (16%) e periaórticos (8,3%). Metástases pulmonares foram encontradas em três pacientes (25%). Metástases para fígado, osso e pele foram observadas em um caso cada (8,3%). Conclusão: A evolução clínica dos pacientes metastáticos com melanoma de sítio primário desconhecido é melhor em relação aos pacientes metastáticos com lesão primária conhecida, quando os dois grupos estão no mesmo estádio. Dessa forma, o fator mais determinante do curso clínico e do prognóstico éa localização das metástases. A maioria dos pacientes que apresenta doença sistêmica ao diagnóstico perde a chance de cura, como muitos pacientes com cutâneo primário fino e doença regional ao diagnóstico.
Introduction: Melanoma is essentially cutaneous. In some patients, it is not possible to determine the location of the primary tumor. The incidence of melanoma of unknown primary site varies from 2 ? 15%. Objectives: To determine whether there is difference in overall survival between patients with known primary melanoma compared to patients with unknown primary melanoma. Methods: A retrospective analysis of patients with melanoma in the database of Surgical Oncology and Digestive Surgery (ONCAD) was performed and identified those with unknown primary site and metastases to different locations. Results: Lymph node was the main site of metastases (50%) - inguinal (25%), axillary (16%) and periaortic (8.3%). Pulmonary metastases were found in three patients ( 25%). Metastasis to the liver, bone and skin were observed in one case each (8.3%). Conclusions: The clinical course of patients with metastatic melanomaof unknown primary site is better than metastatic patients with known primary lesion, when both groups are on the same stage. Thus, the most relevant determining factor affecting clinical course and prognosis is the metastasis location. Most patients presenting systemic disease at diagnosis loses the chance of cure as many patients with thin primary cutaneous and regional disease at diagnosis.
RESUMO
BACKGROUND: In a previous study, we showed that a saponin mixture isolated from the roots of Ampelozizyphus amazonicus Ducke (SAPAaD) reduces urine excretion in rats that were given an oral loading of 0.9 % NaCl (4 ml/100 g body weight). In the present study, we investigated whether atrial natriuretic peptides (ANP) and renal ATPases play a role in the SAPAaD- induced antidiuresis in rats. METHODS: To evaluate the effect of SAPAaD on furosemide-induced diuresis, Wistar rats (250-300 g) were given an oral loading of physiological solution (0.9 % NaCl, 4 ml/100 g body weight) to impose a uniform water and salt state. The solution containing furosemide (Furo, 13 mg/kg) was given 30 min after rats were orally treated with 50 mg/kg SAPAaD (SAPAaD + Furo) or 0.5 ml of 0.9 % NaCl (NaCl + Furo). In the SAPAaD + NaCl group, rats were pretreated with SAPAaD and 30 min later they received the oral loading of physiological solution. Animals were individually housed in metabolic cages, and urine volume was measured every 30 min throughout the experiment (3 h). To investigate the role of ANP and renal Na(+) pumps on antidiuretic effects promoted by SAPAaD, rats were given the physiological solution (as above) containing SAPAaD (50 mg/kg). After 90 min, samples of urine and blood from the last 30 min were collected. Kidneys and atria were also removed after previous anesthesia. ANP was measured by radioimmunoassay (RIA) and renal cortical activities of Na(+)- and (Na(+),K(+))-ATPases were calculated from the difference between the [32P] Pi released in the absence and presence of 1 mM furosemide/2 mM ouabain and in the absence and presence of 1 mM ouabain, respectively. RESULTS: It was observed that SAPAaD inhibited furosemide-induced diuresis (at 90 min: from 10.0 ± 1.0 mL, NaCl + Furo group, n = 5, to 5.9 ± 1.0 mL, SAPAaD + Furo group n = 5, p < 0.05), increased both Na(+)-ATPase (from 25.0 ± 5.9 nmol Pi.mg(-1).min(-1), control, to 52.7 ± 8.9 nmol Pi.mg(-1).min(-1), p < 0.05) and (Na(+),K(+))-ATPase (from 47.8 ± 13.3 nmol Pi.mg(-1).min(-1), control, to 79.8 ± 6.9 nmol Pi .mg(-1).min(-1), p < 0.05) activities in the renal cortex. SAPAaD also lowered urine ANP (from 792 ± 132 pg/mL, control, to 299 ± 88 pg/mL, p < 0.01) and had no effect on plasma or atrial ANP. CONCLUSION: We concluded that the SAPAaD antidiuretic effect may be due to an increase in the renal activities of Na(+)- and (Na(+),K(+))-ATPases and/or a decrease in the renal ANP.
