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  • About
  • The Global ETD Search service is a free service for researchers to find electronic theses and dissertations. This service is provided by the Networked Digital Library of Theses and Dissertations.
    Our metadata is collected from universities around the world. If you manage a university/consortium/country archive and want to be added, details can be found on the NDLTD website.
1

Jaundice Secondary to Isolated Porta Hepatis Metastasis in Colorectal Cancer: Case Report and Review of the Literature

Youssef, Souad S., Kumar, Pullatikurthi Pradeep 01 March 2004 (has links)
Colorectal cancer occurs mainly after the age of 50. The liver is the most frequent site of metastases, although isolated metastases to the porta hepatis are rarely reported in the literature. From 1924 to 1993, only 16 cases of periportal lymph nodes metastases were reported. We report a case of jaundice secondary to porta hepatis metastases from primary colorectal cancer. The appearance of symptoms was concurrent with the elevation of carcinoembryonic antigen in our case. This emphasizes the importance of polymerase chain reaction to detect the small amount of carcinoembryonic antigen transcript in blood or in peritoneal fluid before the appearance of symptoms. Polymerase chain reaction allows the prediction of high risk of recurrence and the presence of micrometastases. More trials are needed to assess the outcome after treatment by adjuvant chemotherapy for micrometastases.
2

Sentinel Node in Clinical Practice : Implications for Breast Cancer Treatment and Prognosis

Andersson, Yvette January 2012 (has links)
The introduction of sentinel lymph node biopsy (SLNB) has conveyed several new issues, such as the risk of false negativity, long-term consequences, the prognostic significance of micrometastases and whether ALND can be omitted in sentinel lymph node- (SLN) positive patients. Archived SLN specimens from 50 false negative patients and 107 true negative controls were serially sectioned and stained with immunohistochemistry. The detection rate of previously unknown metastases did not differ between the false and the true negative patients. The risk of false negativity was higher in patients with multifocal or hormone receptor-negative tumours, or if only one SLN was found. In a Swedish multicentre cohort, 2216 SLN-negative patients in whom ALND was omitted were followed up for a median of 65 months. The isolated axillary recurrence rate was only 1.0%, and the overall survival was high (93%). The survival of 3369 breast cancer patients (2383 node-negative (pN0), 107 isolated tumour cells (pN0(i+), 123 micrometastases (pN1mi) and 756 macrometastases (pN1)) was analysed. The 5-year cause-specific and event-free survival was worse for pN1mi and pN1 patients than for pN0 patients. There was no difference in survival between pN0(i+) and pN0 patients. Tumour and SLN characteristics in 869 SLN-positive patients were compared between those with and without non-SLN metastases, and the Tenon score was calculated. The risk of non-SLN metastases was higher in case of SLN macrometastases (compared with micrometastases), a high positive/total SLN ratio and Elston grade 3 tumours, and increased with increasing tumour size. The area under the curve (AUC) for the Tenon score was 0.65, and the test thus performed inadequately in this population. In conclusion, despite the risk of false negativity, SLNB with omission of ALND in SLN-negative patients appears to be safe even in the long term. The presence of micrometastases is of prognostic importance and should entail adjuvant treatment. The need for ALND in patients with SLN micro- and even macrometastases has been questioned, but the occurrence of non-SLN metastases is hard to predict, and strong evidence for the safe omission of ALND is lacking.
3

Mielopatia infiltrativa por tumores não-hematológicos

Oliveira, Claudia Teresa de [UNESP] 01 April 2009 (has links) (PDF)
Made available in DSpace on 2014-06-11T19:23:07Z (GMT). No. of bitstreams: 0 Previous issue date: 2009-04-01Bitstream added on 2014-06-13T20:29:57Z : No. of bitstreams: 1 oliveira_ct_me_botfm.pdf: 2586546 bytes, checksum: 0fa98dd82d7160414a5cffb84658a089 (MD5) / Fundação Amaral Carvalho / A infiltração de MO por tumores não-hematológicos tem sido descrita desde 1935 e, mais recentemente, desperta interesse da comunidade científica, pois inúmeros trabalhos têm relacionado a presença de células tumorais na MO com o processo de carcinogênese e a progressão tumoral. O presente estudo teve por objetivo o levantamento dos casos com diagnóstico de mielopatia infiltrativa por tumores nãohematológicos, provenientes da Faculdade de Medicina de Botucatu – UNESP e do Hospital Amaral Carvalho – Jaú, avaliados, retrospectivamente, no período de 1998 a 2008 (num universo de 15.191 coletas de MO). Incluímos 193 pacientes, dos quais 171 eram adultos e 22 crianças (idade ≤ 21 anos), com paridade entre os sexos (1:1) e mediana de idade de 55 anos. Foram analisados dados clínicos, diagnóstico e estadiamento do tumor primário, sítios de metástases, características laboratoriais (hemograma e marcadores tumorais séricos), características da MO, tratamento e a relação desses fatores com a sobrevida dos pacientes, através do programa de estatística SPSS®. Os resultados encontrados apontam que os tumores que mais frequentemente infiltraram a MO nos adultos foram: tumores de mama, próstata e sítio primário indeterminado, e neuroblastoma nas crianças. A análise da MO revelou positividade de 80% para mielograma e BMO, e presença de fibrose em 32% dos pacientes (40%, quando associados a áreas de necrose no mesmo material). Na avaliação hematológica observamos: anemia, alteração de leucócitos e plaquetopenia. Houve diferença, estatisticamente significante, com maior mediana de sobrevida global (p= 0,000) para pacientes do sexo feminino, portadores de adenocarcinoma de mama, em estádios iniciais e que receberam algum tipo de tratamento (quimio, radio e/ou hormonioterapia). Na análise de sobrevida, a partir do diagnóstico de mielopatia infiltrativa, houve... / Bone marrow (BM) infiltration by nonhematopoietic tumors has been described since 1935, and a increased number of papers about this topic have been published. Some of the studies have related the relationship between the presence of peripheral circulating tumors cells, bone marrow infiltration, carcinogenesis and tumor progression. This study has, as essential objective, the evaluation of infiltrative mielopathy by nonhematopoietic tumors from Faculdade de Medicina de Botucatu - UNESP and Hospital Amaral Carvalho – Jaú. Data were analised retrospectively from 1998 January to 2008 August (15.191 bone marrow samples). We have included 193 patients. One hundred seventy one were adults and 22 were children (considered age ≤ 21 years), with similar number of patients by gender, and median age 55 years. Medical records from the selected patients were analised, with focus on clinical aspects, primary site of tumor, initial stage, metastatic sites, hematologic and bone marrow features, treatment and the relationship between this data and survival. Results have demonstrated that most frequent solid tumors in adults were breast cancer, prostate cancer and undetermined primary site, and neuroblastoma among children. Bone marrow revealed infiltration in 80% of samples by myelogram and BM biopsy, and fibrosis in 32% (40% when associated with necrosis area). We observed anaemia, leukocyte alterations and thrombocytopenia as hematologic features. There were significant differences in global survival, wich was better among female patients, diagnosis of breast cancer, initial clinical stages and who has received any type of treatment (chemotherapy, radiotherapy and/or hormoniotherapy). When we analised survival since diagnosis of infiltrative mielopathy, adult patients with leucoeritroblastic reaction and trombocytopenia, and undetermined primary site tumors, melanoma or gastrointestinal tumors had... (Complete abstract click electronic access below)
4

Mielopatia infiltrativa por tumores não-hematológicos /

Oliveira, Claudia Teresa de. January 2009 (has links)
Orientador: Lígia Niero-Melo / Banca: Lucilene Silva Ruiz e Rezende / Banca: Eduardo Moreira de Queiroga / Resumo: A infiltração de MO por tumores não-hematológicos tem sido descrita desde 1935 e, mais recentemente, desperta interesse da comunidade científica, pois inúmeros trabalhos têm relacionado a presença de células tumorais na MO com o processo de carcinogênese e a progressão tumoral. O presente estudo teve por objetivo o levantamento dos casos com diagnóstico de mielopatia infiltrativa por tumores nãohematológicos, provenientes da Faculdade de Medicina de Botucatu - UNESP e do Hospital Amaral Carvalho - Jaú, avaliados, retrospectivamente, no período de 1998 a 2008 (num universo de 15.191 coletas de MO). Incluímos 193 pacientes, dos quais 171 eram adultos e 22 crianças (idade ≤ 21 anos), com paridade entre os sexos (1:1) e mediana de idade de 55 anos. Foram analisados dados clínicos, diagnóstico e estadiamento do tumor primário, sítios de metástases, características laboratoriais (hemograma e marcadores tumorais séricos), características da MO, tratamento e a relação desses fatores com a sobrevida dos pacientes, através do programa de estatística SPSS®. Os resultados encontrados apontam que os tumores que mais frequentemente infiltraram a MO nos adultos foram: tumores de mama, próstata e sítio primário indeterminado, e neuroblastoma nas crianças. A análise da MO revelou positividade de 80% para mielograma e BMO, e presença de fibrose em 32% dos pacientes (40%, quando associados a áreas de necrose no mesmo material). Na avaliação hematológica observamos: anemia, alteração de leucócitos e plaquetopenia. Houve diferença, estatisticamente significante, com maior mediana de sobrevida global (p= 0,000) para pacientes do sexo feminino, portadores de adenocarcinoma de mama, em estádios iniciais e que receberam algum tipo de tratamento (quimio, radio e/ou hormonioterapia). Na análise de sobrevida, a partir do diagnóstico de mielopatia infiltrativa, houve... (Resumo completo, clicar acesso eletrônico abaixo) / Abstract: Bone marrow (BM) infiltration by nonhematopoietic tumors has been described since 1935, and a increased number of papers about this topic have been published. Some of the studies have related the relationship between the presence of peripheral circulating tumors cells, bone marrow infiltration, carcinogenesis and tumor progression. This study has, as essential objective, the evaluation of infiltrative mielopathy by nonhematopoietic tumors from Faculdade de Medicina de Botucatu - UNESP and Hospital Amaral Carvalho - Jaú. Data were analised retrospectively from 1998 January to 2008 August (15.191 bone marrow samples). We have included 193 patients. One hundred seventy one were adults and 22 were children (considered age ≤ 21 years), with similar number of patients by gender, and median age 55 years. Medical records from the selected patients were analised, with focus on clinical aspects, primary site of tumor, initial stage, metastatic sites, hematologic and bone marrow features, treatment and the relationship between this data and survival. Results have demonstrated that most frequent solid tumors in adults were breast cancer, prostate cancer and undetermined primary site, and neuroblastoma among children. Bone marrow revealed infiltration in 80% of samples by myelogram and BM biopsy, and fibrosis in 32% (40% when associated with necrosis area). We observed anaemia, leukocyte alterations and thrombocytopenia as hematologic features. There were significant differences in global survival, wich was better among female patients, diagnosis of breast cancer, initial clinical stages and who has received any type of treatment (chemotherapy, radiotherapy and/or hormoniotherapy). When we analised survival since diagnosis of infiltrative mielopathy, adult patients with leucoeritroblastic reaction and trombocytopenia, and undetermined primary site tumors, melanoma or gastrointestinal tumors had... (Complete abstract click electronic access below) / Mestre
5

Prognostic factors in colorectal cancer : aspects of tumour dissemination

Öberg, Åke January 2002 (has links)
<p>Diss. (sammanfattning) Umeå : Umeå universitet, 2002</p> / digitalisering@umu

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