Le cancer surrénalien est classiquement associé à un pronostic morne. Pourtant sa présentation clinique change. De nouvelles perspectives ont émergé sur ses mécanismes pathophysiologiques (par l'élucidation génétique des syndromes familiaux). Et les centres de référence dans les réseaux nationaux et européens offrent maintenant une prise en charge clinique multidisciplinaire, mais aussi plus normalisée et plus efficace, de ces patients difficiles. Tous les aspects des cancers surrénaliens sont abordés dans cet ouvrage par des experts en chaque domaine : l'épidémiologie, le pronostic, la prise en charge clinique, la pathologie, les mécanismes pathophysiologiques moléculaires, les approches modernes de l'imagerie, les traitements chirurgicaux et chimiothérapeutiques des lésions primaires et secondaires, et les aspects particuliers du carcinome cortical surrénal chez l'enfant. Cet ouvrage, illustré de nombreuses figures et photographies, sera d'un intérêt majeur pour les endocrinologues, radiologues et spécialistes de la médecine nucléaire, chirurgiens, oncologues, pédiatres. Adrenal Cortical Carcinoma is classically associated with a dismal prognosis. Yet its clinical presentation is changing (more and more classified as "incidentaloma"). New insights have emerged on its pathophysiological mechanisms (through the genetic elucidation of familial syndromes), and Reference Centers within National and European Networks are now offering more standardized and efficient multidisciplinary clinical management of these difficult patients. All these important aspects are described by experts in nine chapters dealing with epidemiology, prognosis, and clinical management, pathology, molecular pathophysiological mechanisms, modern imaging approaches, surgical and chemotherapeutical approaches of primary and secondary lesions, and the particular aspects of adrenal cortical carcinoma in children. This book, with its many figures and photographs, will be of major interest to endocrinologists, radiologists and nuclear medicine experts, pathologists, surgeons, oncologists, pediatricians. After a thorough reading, one will better recognize a suspicious adrenal "incidentaloma", diagnose steroid hypersecretion, suspect a familial disease, consult with the pathologist and surgeon, manipulate difficult drugs like 0,p'DDD, participate in multidisciplinary discussions with oncologists, radiotherapeutists, molecular biologists... Modern medicine in action!
Les informations fournies dans la section « Synopsis » peuvent faire référence à une autre édition de ce titre.
Le cancer surrénalien est classiquement associé à un pronostic morne. Pourtant sa présentation clinique change. De nouvelles perspectives ont émergé sur ses mécanismes pathophysiologiques (par l'élucidation génétique des syndromes familiaux). Et les centres de référence dans les réseaux nationaux et européens offrent maintenant une prise en charge clinique multidisciplinaire, mais aussi plus normalisée et plus efficace, de ces patients difficiles. Tous les aspects des cancers surrénaliens sont abordés dans cet ouvrage par des experts en chaque domaine : l'épidémiologie, le pronostic, la prise en charge clinique, la pathologie, les mécanismes pathophysiologiques moléculaires, les approches modernes de l'imagerie, les traitements chirurgicaux et chimiothérapeutiques des lésions primaires et secondaires, et les aspects particuliers du carcinome cortical surrénal chez l'enfant. Cet ouvrage, illustré de nombreuses figures et photographies, sera d'un intérêt majeur pour les endocrinologues, radiologues et spécialistes de la médecine nucléaire, chirurgiens, oncologues, pédiatres. Adrenal Cortical Carcinoma is classically associated with a dismal prognosis. Yet its clinical presentation is changing (more and more classified as "incidentaloma"). New insights have emerged on its pathophysiological mechanisms (through the genetic elucidation of familial syndromes), and Reference Centers within National and European Networks are now offering more standardized and efficient multidisciplinary clinical management of these difficult patients. All these important aspects are described by experts in nine chapters dealing with epidemiology, prognosis, and clinical management, pathology, molecular pathophysiological mechanisms, modern imaging approaches, surgical and chemotherapeutical approaches of primary and secondary lesions, and the particular aspects of adrenal cortical carcinoma in children. This book, with its many figures and photographs, will be of major interest to endocrinologists, radiologists and nuclear medicine experts, pathologists, surgeons, oncologists, pediatricians. After a thorough reading, one will better recognize a suspicious adrenal "incidentaloma", diagnose steroid hypersecretion, suspect a familial disease, consult with the pathologist and surgeon, manipulate difficult drugs like 0,p'DDD, participate in multidisciplinary discussions with oncologists, radiotherapeutists, molecular biologists... Modern medicine in action!
Adrenal Cortical Carcinoma is classically associated with a dismal prognosis. Yet its clinical presentation is changing (more and more classified as "incidentaloma"). New insights have emerged on its pathophysiological mechanisms (through the genetic elucidation of familial syndromes), and Reference Centers within National and European Networks are now offering more standardized and efficient multidisciplinary clinical management of these difficult patients. All the important aspects are described by experts in nine chapters dealing with epidemiology, prognosis, and clinical management, pathology, molecular pathophysiological mechanisms, modern approaches, surgical and chemotherapeutical approaches of primary and secondary lesions, and the particular aspects of adrenal cortical carcinoma in children. This book, with its many figures and photographs, will be of major interest to endocrinologists, radiologists and nuclear exerts, pathologists, surgeons, oncologists, pediatricians. After a thorough reading, one will be better recognize a suspicious adrenal "incidentaloma", diagnose steroid hypersecretion, suspect a familial disease, consult with the pathologist and surgeon, manipulate difficult drugs like O,p'DDD, participate in multidisciplinary discussions with oncologists, radiotherapeutists, molecular biologists... Modern medicine in action!
Les informations fournies dans la section « A propos du livre » peuvent faire référence à une autre édition de ce titre.
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Paperback. Etat : new. Paperback. Adrenal Cortical Carcinoma is classically associated with a dismal prognosis. Yet its clinical presentation is changing (more and more classified as 'incidentaloma'). New insights have emerged on its pathophysiological mechanisms (through the genetic elucidation of familial syndromes), and Reference Centers within National and European Networks are now offering more standardised and efficient multidisciplinary clinical management of these difficult patients. All these important aspects are described by experts in nine chapters dealing with epidemiology, prognosis, and clinical management, pathology, molecular pathophysiological mechanisms, modern imaging approaches, surgical and chemotherapeutical approaches of primary and secondary lesions, and the particular aspects of adrenal cortical carcinoma in children. This book, with its many figures and photographs, will be of major interest to endocrinologists, radiologists and nuclear medicine experts, pathologists, surgeons, oncologists, paediatricians.After a thorough reading, one will better recognise a suspicious adrenal 'incidentaloma', diagnose steroid hypersecretion, suspect a familial disease, consult with the pathologist and surgeon, manipulate difficult drugs like O,p'DDD, participate in multidisciplinary discussions with oncologists, radiotherapeutists, molecular biologists.Modern medicine in action! Adrenal Cortical Carcinoma is classically associated with a dismal prognosis. Yet its clinical presentation is changing. This book, with its many figures and photographs, helps you better recognise a suspicious adrenal 'incidentaloma', diagnose steroid hypersecretion, suspect a familial disease, and, manipulate difficult drugs like O,p'DDD. Shipping may be from multiple locations in the US or from the UK, depending on stock availability. N° de réf. du vendeur 9782742005932
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Etat : New. Editor(s): Bertagna, Xavier. Num Pages: 133 pages, colour & b/w photos. BIC Classification: MJCL. Category: (P) Professional & Vocational. Dimension: 239 x 169 x 8. Weight in Grams: 288. . 2006. 1st. Paperback. . . . . N° de réf. du vendeur V9782742005932
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