Neoplasia papilar cística do pâncreas

dc.contributor.authorPinto Junior, Francisco Edilson Leite
dc.contributor.authorMoraes, Marcus Vinícius de
dc.contributor.authorOliveira, Álisson Giovani Freitas de
dc.date.accessioned2013-08-07T15:24:37Z
dc.date.available2013-08-07T15:24:37Z
dc.date.issued2001
dc.description.abstractPapyllary cystic tumor of the pancreas, so-called Frantz’s tumor, is rare. Clinical presentation of this disease is usually a slowly growing abdominal mass with or without abdominal pain, affecting predominantly young females. Its pathogenesis is still unknown . Surgical resection is usually curative, and prognosis is excellent. The authors report two pancreatic tumor cases(Frantz’s tumor) in women aged 26 and 31 years old. Pre operative assessment showed a solid-cystic tumor of the tail and body of the pancreas. An extended distal pancreatectomy was performed without splenic preservationpt_BR
dc.identifier.citationPINTO JÚNIOR, Francisco Edilson Leite; MORAES, M. V. ; Álisson Giovani Freitas de Oliveira. Neoplasia papilar cística do pâncreas. Revista do Colégio Brasileiro de Cirurgiões, v. 28, p. 304-306, 2001.pt_BR
dc.identifier.urihttps://repositorio.ufrn.br/jspui/handle/1/6256
dc.language.isoporpt_BR
dc.publisherRevista do Colégio Brasileiro de Cirurgiõespt_BR
dc.rightsAcesso Abertopt_BR
dc.subjectFrantz’s tumorpt_BR
dc.subjectPancreatic tumorpt_BR
dc.titleNeoplasia papilar cística do pâncreaspt_BR
dc.title.alternativePapyllary cystic tumor of the pancreaspt_BR
dc.typearticlept_BR

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