Feuillets De Radiologie最新文献

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Congrès et Enseignements 大会与教学
Feuillets De Radiologie Pub Date : 2016-10-01 DOI: 10.1016/S0181-9801(16)30127-0
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引用次数: 0
FMC : AutoévaluationLes calcifications cérébrales : du normal au pathologique 脑钙化:从正常到病理
Feuillets De Radiologie Pub Date : 2016-10-01 DOI: 10.1016/j.frad.2016.06.002
G. Sebti, A. Zentar, S. Alj, M. O. Idrissi, N. C. Idrissi
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引用次数: 0
CV2i Editorial board CV2i编委会
Feuillets De Radiologie Pub Date : 2016-09-01 DOI: 10.1016/S0181-9801(16)30088-4
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引用次数: 0
Douleur lombaire et cervicale 腰痛和颈椎痛
Feuillets De Radiologie Pub Date : 2016-09-01 DOI: 10.1016/j.frad.2016.03.012
H. Sahli , I. Cherif , R. Tekaya , I. Nackache , A. Farah , I. Mahmoud
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引用次数: 0
Douleurs plantaires chez une femme de 43 ans 43岁女性足底疼痛
Feuillets De Radiologie Pub Date : 2016-09-01 DOI: 10.1016/j.frad.2016.01.002
S. Alj , M. Ouali Idrissi , N. Cherif Idrissi El Ganouni
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引用次数: 1
Quel est votre diagnostic ?Para-paresthésie sans trouble sphinctérien chez un patient ayant bénéficié d’une transplantation rénale 你的诊断是什么?肾移植患者无括约肌障碍的感觉异常
Feuillets De Radiologie Pub Date : 2016-09-01 DOI: 10.1016/j.frad.2016.02.001
L. Benzaouia, A. Siwane, J. Dinari, S. Lezar, F. Essodegui
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引用次数: 0
Tumeur médiastinale inhabituelle 异常纵隔肿瘤
Feuillets De Radiologie Pub Date : 2016-09-01 DOI: 10.1016/j.frad.2016.05.009
M. Abdellaoui, S. Khnaba, M. Jidal, A. Darbi, T. Amil
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引用次数: 0
Plaidoyer pour un enseignement de l’éthique plus approfondi dans la formation initiale de manipulateur en électroradiologie médicale. Mise au point sur la formation de manipulateur en électroradiologie médicale 倡导在医学电放射学操作人员的初步培训中进行更深入的伦理教学。医学电放射学机械手训练的发展
Feuillets De Radiologie Pub Date : 2016-09-01 DOI: 10.1016/j.frad.2016.05.012
C. Gesbert, M.-F. Mamzer, C. Hervé
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引用次数: 1
Para-paresthésie sans trouble sphinctérien chez un patient ayant bénéficié d’une transplantation rénale 肾移植患者无括约肌障碍的感觉异常
Feuillets De Radiologie Pub Date : 2016-09-01 DOI: 10.1016/j.frad.2016.02.001
L. Benzaouia, A. Siwane, J. Dinari, S. Lezar, F. Essodegui
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引用次数: 0
Imagerie de la neurofibromatose de type 1 1型神经纤维瘤的影像
Feuillets De Radiologie Pub Date : 2016-09-01 DOI: 10.1016/j.frad.2016.05.013
M. Koob , J.-L. Dietemann
{"title":"Imagerie de la neurofibromatose de type 1","authors":"M. Koob ,&nbsp;J.-L. Dietemann","doi":"10.1016/j.frad.2016.05.013","DOIUrl":"https://doi.org/10.1016/j.frad.2016.05.013","url":null,"abstract":"<div><p>La neurofibromatose de type 1 est la plus fréquente des phacomatoses et des neurofibromatoses, avec une incidence de 1/2500 naissances. Transmise sur le mode autosomique dominant, elle se traduit par la présence de tumeurs principalement cutanées, cérébrales et des nerfs périphériques, et par des dysplasies osseuses et vasculaires. Les lésions cutanées les plus caractéristiques de la maladie sont les taches café au lait et les neurofibromes cutanés. Les neurofibromes de topographie interne peuvent entraîner diverses complications, la plus grave étant la dégénérescence en tumeur maligne des gaines nerveuses périphériques, qui est la principale cause de mortalité précoce de la maladie. Le gliome des voies optiques, observé chez l’enfant, est un astrocytome pilocytique peu évolutif. Les hamartomes cérébraux sont fréquents, bénins, et disparaissent après l’âge de 20 ans. Les scolioses dystrophiques, souvent associées à des neurofibromes et à une dysplasie durale, provoquent souvent des complications orthopédiques et neurologiques. Les dysplasies vasculaires entraînent des sténoses artérielles progressives, principalement cérébrales et rénales. La sévérité de la maladie est variable selon les patients et imprévisible. L’imagerie a un rôle important dans le diagnostic et le suivi des complications de la maladie, qui surviennent pour la plupart dans l’enfance.</p></div><div><p>Neurofibromatosis type 1 (NF1) is the most common phakomatosis and neurofibromatosis, with an incidence of 1 per 2500 births. This autosomal dominant disease is characterized by tumors affecting the skin, the brain and the peripheral nerves, and by bone and vascular dysplasia. The most characteristic skin lesions of the disease are café au lait spots and cutaneous neurofibromas. Deep neurofibromas cause various complications, the most serious being degeneration of malignant peripheral nerve sheath tumors, the leading cause of premature disease-related mortality. Optic gliomas are slow-growing pilocytic astrocytomas that occur in children. Brain hamartomas are common, benign and disappear after the age of 20. Dystrophic scoliosis is often associated with neurofibromas and dural dysplasia, and causes orthopedic and neurological complications. Vascular dysplasia leads to progressive arterial stenosis, mainly in the brain and the kidneys. The severity of the disease varies widely from patient to patient and is unpredictable. Imaging has an important role in confirming the diagnosis and detecting complications that occur mostly in childhood.</p></div>","PeriodicalId":50450,"journal":{"name":"Feuillets De Radiologie","volume":"56 4","pages":"Pages 199-214"},"PeriodicalIF":0.0,"publicationDate":"2016-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.frad.2016.05.013","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"71796938","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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