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Authordc.contributor.authorUrdangarín, Angélica 
Authordc.contributor.authorIñíguez Vila, Germán es_CL
Authordc.contributor.authorBenavides Castillo, Carlos es_CL
Authordc.contributor.authorCastillo, Cecilia es_CL
Authordc.contributor.authorCastro, Alex es_CL
Authordc.contributor.authorCastillo Montecinos, Iván es_CL
Authordc.contributor.authorCorredoira Salum, Yamile es_CL
Authordc.contributor.authorSoto, Néstor es_CL
Admission datedc.date.accessioned2010-11-25T18:45:23Z
Available datedc.date.available2010-11-25T18:45:23Z
Publication datedc.date.issued2010-07
Cita de ítemdc.identifier.citationREVISTA MEDICA DE CHILE Volume: 138 Issue: 7 Pages: 841-846 Published: JUL 2010en_US
Identifierdc.identifier.issn0034-9887
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/128796
Abstractdc.description.abstractNeuroendocrine tumors are uncommon, including VIPoma that produces vasoactive intestinal polypeptide. We report a 45-year-old female presenting with a history of diarrhea lasting three months. An abdominal CAT scan showed a solid tumor in the body of the pancreas. A fine needle aspiration biopsy of the tumor was compatible with a neuroendocrine tumor. The patient was subjected to a partial pancreatectomy, excising a 4 cm diameter tumor. The pathological study was compatible with a neuroendocrine carcinoma. There was no regional lymph node involvement. During the postoperative period the results of serum vasoactive intestinal polypeptide were received. These were 815.9 pg/ml before surgery and normalized after the operation.en_US
Lenguagedc.language.isoesen_US
Publisherdc.publisherSOC MEDICA SANTIAGOen_US
Keywordsdc.subjectPancreatic neoplasmsen_US
Títulodc.titleVIPoma pancreático. Caso clínicoen_US
Title in another languagedc.title.alternativePancreatic VIPoma. Report of one caseen_US
Document typedc.typeArtículo de revista


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