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Multidisciplinary surgical management of Cowden syndrome: report of a case

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Multidisciplinary surgical management of Cowden syndrome: report of a case

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dc.contributor.author Patini, Romeo es
dc.contributor.author Staderini, Edoardo es
dc.contributor.author Gallenzi, Patrizia es
dc.date.accessioned 2017-03-06T08:32:17Z
dc.date.available 2017-03-06T08:32:17Z
dc.date.issued 2016 es
dc.identifier.citation Patini, Romeo ; Staderini, Edoardo ; Gallenzi, Patrizia. Multidisciplinary surgical management of Cowden syndrome: report of a case. En: Journal of Clinical and Experimental Dentistry. 2016. Vol. 8, no. 4: 472 es
dc.identifier.uri http://hdl.handle.net/10550/57543
dc.description.abstract Cowdenâ s Syndrome (CS) is a rare congenital autosomal dominant disorder that affects around 1/200000 patients with an incomplete penetrance and variable expressivity, characterized by alterations in a tumor suppressor gene. A 14-year-old Caucasian male patient came to the attention of the authors complaining of palm nodules, gingival bleeding and painful pedunculated lesions on the lips and on the labial side of anterior sextants. After genetic investigation the final diagnosis of a Cowden Syndrome was made. The lesions were surgically removed under general anesthesia and no clinical signs of recurrence were found three months after surgical excision. Considering the severe symptoms of the syndrome and the strong tendency to malignant development of the associated lesions all clinicians should focus their efforts to the early diagnosis and, when possible, multidisciplinary treatment. en_US
dc.subject Odontología es
dc.subject Ciencias de la salud es
dc.title Multidisciplinary surgical management of Cowden syndrome: report of a case es
dc.type journal article es_ES
dc.subject.unesco UNESCO::CIENCIAS MÃ DICAS es
dc.type.hasVersion VoR es_ES

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