dc.creatorBeltrán,Marcelo A
dc.creatorBarría,Carlos
dc.creatorContreras,Mario A
dc.creatorWilson,Christian S
dc.creatorCruces,Karina S
dc.date2009-09-01
dc.date.accessioned2017-03-07T16:16:28Z
dc.date.available2017-03-07T16:16:28Z
dc.identifierhttp://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0034-98872009000900009
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/398872
dc.descriptionNeurofibromatosis Type 1 (NF1) is an autosomic dominant condition affecting the central nervous systema and presenting a disposition towards development of gastrointestinal stromal tumors (GIST). We report a 38year-old female patient with neurofibromatosis type 1 that required emergency surgery due to a perforated GIST originating in the fourth duodenal portion. The GIST, and the fourth duodenal portion, were excised and a primary duodenum-jejunal anastomosis was performed. The pathological study showed a partially necrotic solid-cystic tumor with 1 to 2 mitoses per 50-high-power fields. The cells stained positively to CD 117, CD34 and Desmin, and were negative to S-100, Vimentin, and Smooth Muscle a-Actin. The patient is currently asymptomatic and under follow-up during the last 11 months after surgery (Rev Méd Chile 2009; 137:1197-200).
dc.formattext/html
dc.languagees
dc.publisherSociedad Médica de Santiago
dc.sourceRevista médica de Chile v.137 n.9 2009
dc.subjectGastrointestinal stromal tumors
dc.subjectNeurofibromatosis 1
dc.subjectProtein kinase inhitors
dc.titleTumor del estroma gastrointestinal (GIST) en una paciente con neurofibromatosis tipo 1
dc.typeArtículos de revistas


Este ítem pertenece a la siguiente institución