OBJECTIVE: The present study aims to report the preliminary experience with videolaparoscopic retroperitoneal lymphadenectomy in the treatment of patients with non-siinomatous testicular tumor. MATERIALS AND METHODS: Seven surgeries were performed in order to access retroperitoneal lymph nodes in patients with non-siinomatous testicular cancer. We performed the videolaparoscopic retroperitoneal lymphadenectomy (LRL) technique in 5 patients with stage I disease and laparoscopic resection of residual mass (LRRM), following chiotherapy (ChT), in 2 patients with stage II disease. Initial approach was obtained through 4 trocars, using an incision in supra-umbilical midline when manual assistance was required. Surgical time was analyzed, as well as blood loss, need for analgesic drugs postoperatively, hospital stay, complications, need for blood transfusion, histopathological data and tumor control in a mean follow-up of 18 months. RESULTS: Mean surgical time was 200 to 260 minutes in LRL and LRRM groups respectively, mean blood loss was 300 mL for the LRL group and 400 mL for the LRRM group, without need for transfusions. There was a lesion in the vena cava in the LRL group, which was managed with manual assistance and one conversion in the LRRM group, due to a 10-cm tumor mass that was adhered to the aorta. Mean hospital stay was 3 days, excluding the converted case, and the use of analgesic drugs was needed until the second postoperative day. Of the stage I patients, 2 had active disease in retroperitoneum, and underwent adjuvant ChT. The 2 residual masses were teratomas. There was no recurrence during the follow-up period. CONCLUSIONS: Videolaparoscopic retroperitoneal lymphadenectomy is a procedure with high technical complexity and a higher potential for conversion when performed following chiotherapy.

Fibras poliméricas têm sido utilizadas com sucesso para o aumento da resistência ao dano de concretos refratários durante a secagem. Tal aplicação se baseia no aumento de permeabilidade ocasionado pela fusão ou degradação dessas fibras durante o primeiro aquecimento do concreto. Além desse benefício, as fibras poliméricas podem também atuar como reforço, aumentando tanto a resistência mecânica quanto a energia total de fratura, se suas propriedades se mantiverem íntegras até a temperatura de máxima pressurização. Este trabalho tem como objetivo avaliar a resistência mecânica e a energia total de fratura de concretos úmidos e secos, reforçados com diferentes tipos de fibras poliméricas. Verificou-se um grande aumento das propriedades mecânicas com a adição de fibras, sendo que a influência do tipo de fibra adicionado mostrou-se mais acentuada nos ensaios realizados com o concreto seco. Os resultados ajudam a explicar o comportamento dos concretos com fibras durante a etapa de secagem.

Polymeric fibers have been successfully used in order to improve refractory castables' performance during drying. There is a well-known permeability improvement brought upon by these fibers' melting or degradation, during heat up. Additionally, fibers can also provide mechanical reinforcement, increasing the material's strength and its work of fracture, but only if they are not weakened by heat up to the temperature of maximum pressurization of steam. In this paper, the mechanical strength of fiber-containing castables and the work of fracture are greatly increased by the use of short fibers, and these properties were well related to the materials' behavior during drying.

An experimental study on solidification structure development and on endogenous inclusion precipitation in a continuously cast resulphurised steel is presented. Results were obtained by investigating two heats of a free cutting C-Mn steel cast in billets with a diameter of 145 mm. The as cast structure was evaluated by macro- and microscopic analyses. Primary and secondary dendrite arm spacing measurement allowed to estimate the solidification time experienced by the steel in different region of the billet section. Modification of the pearlite vs. ferrite fraction was also studied as a function of distance from billet surface and thus with reference to solidification conditions. Endogenous inclusions of the type MnS and CaO-Al2O3 were analysed. Their formation was discussed as a function of the composition of the heats. Also for the inclusions resulting after steel solidification, the data suggested that the effects of local solidification condition and of segregation played a role of primary importance.

A infusão de células hematopoéticas totipotentes criopreservadas permite a recuperação da hematopoese após quimioterapia mieloablativa. OBJETIVO. A formação de cristais de gelo durante o processo de congelamento é o fator principal que causa ruptura das estruturas celulares. A criopreservação dessas células a uma taxa constante preveniria os danos causados pelo congelamento brusco. MÉTODOS. Vinte e três pacientes com mediana de 25 anos (variação 3-57) tiveram a medula óssea e/ou células-tronco periféricas (CTP) coletadas no período de março de 1993 a outubro de 1994, totalizando 86 congelamentos. Os pacientes apresentavam as seguintes neoplasias: linfoma não-Hodgkin (n=5), leucemia mielóide aguda (n=8), leucemia linfóide aguda (n=6), doença de Hodgkin (n=3) e mieloma múltiplo (n=1). O congelamento foi controlado por um computador, acoplado ao sistema, às seguintes temperaturas: -1°C/min até -45°C e depois a -10°C/min até -80°C. Após o congelamento, as células foram mantidas em freezer a -110°C até o momento da infusão. Para obtenção das CTP, empregou-se o fator de crescimento estimulante de granulócitos (G-CSF). RESULTADOS. Uma mediana de 3,16 x 10(8) céls./kg (variação 0,86-24,22) de CTP e 2,03 x 10(8) céls./kg (variação 0,19-12,21) de medula óssea foi congelada. A mediana para atingir granulócitos maior ou igual a 500/µL e plaquetas maior que 20.000/µL foi de 12 dias (variação 8-40) e 31 dias (variação 8-80), respectivamente. Todos os pacientes tiveram recuperação hematopoética após a infusão das células criopreservadas. CONCLUSÃO. A criopreservação em congelador programável permite o armazenamento de células hematopoéticas e, potencialmente, pode causar menor dano celular.

The cryopreservation of hematopoietic stem cells can be used for rescuing the hematopoiesis after high dose chemotherapy. PURPOSE. The ice cristal formation during the freezing procedure is the key point that can be harmful to the cells. The cryopreservation of hematopoietic stem cells in a controlled-rate freezer could decrease the cell damage. METHODS. Twenty-three patients with a median age of 26 years (range 03-57) had bone marrow and/or peripheral blood stem cells harvested from March 1993 through October 1994, ending up to 86 freezing procedures. The patient's diagnoses are as follows: Non-Hodgkin's Lymphoma (n=5); Acute Myelogenous Leukemia (n=8); Acute Lymphocytic Leukemia (n=6); Hodgkin's disease (n=3); Multiple Myeloma (n=1). The cells were frozen away in a controlled-rate freezer chamber at the folowing rate: -1°C/min from room temperature to -45°C and then, at -10°C/min down to -80°C. After freezing, the cells were kept into mechanical freezers until the marrow infusion. To mobilize PBSC (peripheral blood stem cells), G-CSF (granulocyte colony stimulating factor) was given. RESULTS. A median of 3.16x10(8) cells/kg (range 0.86-24.22) of PBSC and 2.03x10(8) cells/kg (0.19-12.21) of bone marrow cells were frozen. The median time to reach granulocytes greater than 500/µL and platelets greater than 20,000/µL was 12 days (range 8-40) and 31 days (range 8-80), respectively. All patients had marrow engraftment after infusion of hematopoietic stem cells. CONCLUSION. The cryopreservation procedure using a controlled-rate freezer can store hematopoietic stem cells and potentially, cause less damage to the cells.