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dc.creatorRodríguez G,Cristián
dc.creatorCarrión A,Flavio
dc.creatorMarinovic M,María Angélica
dc.creatorChávez C,Eduardo
dc.creatorPreisler R,Jessica
dc.creatorPooley B,Francisco
dc.creatorFutatani,Takeshi
dc.creatorOchs,Hans D
dc.date2003-03-01
dc.date.accessioned2019-11-14T12:59:05Z
dc.date.available2019-11-14T12:59:05Z
dc.identifierhttps://scielo.conicyt.cl/scielo.php?script=sci_arttext&pid=S0034-98872003000300009
dc.identifier.urihttps://revistaschilenas.uchile.cl/handle/2250/119280
dc.descriptionWe report a 11 years old male diagnosed as a X-linked hyper-IgM syndrome that presented with recurrent infections and sclerosing cholangitis and later developed a gallbladder cancer. Immunological evaluation showed decreased levels of serum IgG and IgA with elevated levels of IgM. Study of CD40 ligand expression on mitogen activated peripheral blood mononuclear cells revealed total absence of this marker on T lymphocytes. Molecular analysis detected, in the patient and his mother, a nonsense mutation in exon 1 of the transmembrane segment of the CD40 ligand. He also presented elevation of alkaline phosphatases and mild elevation of liver enzymes. Liver biopsy demonstrated the presence of idiopathic sclerosing cholangitis. The patient was started on monthly IVIG therapy at 400 mg/kg, as well as ursodeoxycholic acid and vitamin E, with normalization of his IgG and IgM levels a decrease in the incidence of infections and normalization of liver function. Three years after diagnosis, we detected the presence of polyps inside the gallbladder that were reported at biopsy as adenocarcinoma. He underwent hepatic bisegmentectomy (VI B-V) and local lymphadenectomy (Rev Méd Chile 2003; 131: 303-8).
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dc.publisherSociedad Médica de Santiago
dc.relation10.4067/S0034-98872003000300009
dc.rightsinfo:eu-repo/semantics/openAccess
dc.sourceRevista médica de Chile v.131 n.3 2003
dc.subjectCholangitis, Sclerosing
dc.subjectGallbladder, neoplasms
dc.subjectIgM
dc.titleSíndrome de hiper-IgM asociado a colangitis esclerosante y neoplasia vesicular: Caso clínico


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