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  • av Wala Ben Kridis
    627,-

    Bei Kindern machen paratestikuläre Tumoren etwa 1-2% der soliden Tumoren aus, mit einer Inzidenz von 0,5-2 pro 100.000 Kinder. Der häufigste pathologisch-anatomische Typ bei Kindern ist das Rhabdomyosarkom, andere Typen von Paratumoren sind die Ausnahme. In den meisten Fällen werden diese Tumoren nicht erkannt und manchmal anfänglich falsch diagnostiziert. Diese Tumoren erfordern eine multidisziplinäre Behandlung, um das Überleben der Betroffenen zu verbessern. Die Behandlung ist unabhängig von der Art des Tumors und des Stadiums hauptsächlich chirurgisch und erfordert je nach Tumor und Tumorausdehnung häufig eine Chemotherapie.

  • av Wala Ben Kridis
    627,-

    Nas crianças, os tumores paratesticulares representam aproximadamente 1-2% dos tumores sólidos, com uma incidência de 0,5-2 por 100.000 crianças. O tipo anatomopatológico mais comum nas crianças é o rabdomiossarcoma, sendo os outros tipos de tumores paratesticulares excepcionais. Na maioria dos casos, estes tumores não são reconhecidos e, por vezes, são inicialmente mal diagnosticados. Estes tumores requerem um tratamento multidisciplinar para melhorar a sobrevivência dos doentes. O tratamento é essencialmente cirúrgico, independentemente do tipo e do estádio do tumor, e muitas vezes requer quimioterapia, consoante o tumor e a sua extensão.

  • av Wala Ben Kridis
    627,-

    In children, paratesticular tumors represent approximately 1-2% of solid tumors, with an incidence of 0.5-2 per 100,000 children. The most frequent anatomopathological type in children is rhabdomyosarcoma, and other types of paratesticular tumours are exceptional. In most cases, these tumors are unrecognized and sometimes initially misdiagnosed. These tumors require multidisciplinary management to improve patient survival. Treatment is essentially surgical, irrespective of tumour type and stage, and often requires chemotherapy depending on the tumour and tumour extension.

  • av Wala Ben Kridis
    627,-

    Nei bambini, i tumori paratesticolari rappresentano circa l'1-2% dei tumori solidi, con un'incidenza di 0,5-2 per 100.000 bambini. Il tipo anatomopatologico più comune nei bambini è il rabdomiosarcoma, mentre altri tipi di tumore paratesticolare sono eccezionali. Nella maggior parte dei casi, questi tumori non vengono riconosciuti e talvolta sono inizialmente diagnosticati in modo errato. Questi tumori richiedono una gestione multidisciplinare per migliorare la sopravvivenza del paziente. Il trattamento è essenzialmente chirurgico, indipendentemente dal tipo e dallo stadio del tumore, e spesso richiede la chemioterapia a seconda del tumore e della sua estensione.

  • av Wala Ben Kridis
    612,-

    Chez les enfants, les tumeurs paratesticulaires représentent approximativement 1- 2 % des tumeurs solides avec une incidence de 0,5-2 par 100 000 enfants. Le type anatomopathologique le plus fréquent chez les enfants est le rhabdomyosarcome et les autres types des tumeurs paratesticulaires sont exceptionnels. Dans la plupart des cas, ces tumeurs sont méconnues et parfois mal diagnostiquées initialement. Ces tumeurs nécessitent une prise en charge multidisciplinaire afin d¿améliorer la survie des malades. Le traitement est essentiellement chirurgical indépendamment du type de la tumeur et du stade et nécessite souvent une chimiothérapie en fonction de la tumeur et de l¿extension tumoral.

  • av Wala Ben Kridis
    642,-

    Breast cancer is the first cancer of women in the world and in Tunisia with an incidence of 46.3 and 37.8 cases / 100 000 inhabitants per year respectively. It is the second cause of cancer mortality in women in Tunisia with 17 deaths / 100 000 inhabitants per year.The management of metastatic breast cancer has undergone several advances over the past decades leading to an improvement in patient survival. However, 15 to 30% of patients will develop brain metastases (BM) during their disease. They can occur synchronously (at the time of diagnosis of the primary cancer) or metachronously (after 6 months of the end of the primary cancer treatment). The management of CD is multidisciplinary, involving neurologists, neurosurgeons, radiologists, radiation oncologists, medical oncologists and pathologists.Radiation therapy (RT) is one of the pillars of CD treatment and has long been the standard treatment with its different modalities.The place of surgery is discussed according to the operability and resectability of metastases, as well as the status of systemic disease.Systemic treatment can be based on chemotherapy, hormonal therapy and targeted therapy and depends on the terrain, molecular classification and previously prescribed treatments.

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