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dc.contributor.authorYazici, Mutlu Uysal
dc.contributor.authorEkinci, Saniye
dc.contributor.authorTurkmen, Ozlem Keskin
dc.contributor.authorYalcin, Ebru Gunes
dc.contributor.authorCiftci, Arbay O.
dc.contributor.authorGucer, Safak
dc.contributor.authorOrhan, Diclehan
dc.contributor.authorTezcan, Ilhan
dc.date.accessioned2019-12-12T06:44:41Z
dc.date.available2019-12-12T06:44:41Z
dc.date.issued2014
dc.identifier.issn2194-7619
dc.identifier.urihttps://doi.org/10.1055/s-0033-1354745
dc.identifier.urihttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4335950/
dc.identifier.urihttp://hdl.handle.net/11655/16892
dc.description.abstractSplit notochord syndrome is a rare group of developmental abnormalities caused by abnormal splitting or deviation of the notochord clinically resulting in the duplicated bowel associated with vertebral anomalies. We report on a case of 11-month-old female infant with mediastinal hyperechogenic cyst and intestinal duplication cyst associated with T5-T6 hemivertebrae, scoliosis, and nonfusion of posterior part of T6 vertebrae, presenting with severe hemoptysis and hematemesis. The cysts were surgically removed, and histopathologic analysis revealed that the mediastinal cyst was lined by gastric mucosa and intestinal one was lined with gastric mucosa including ectopic pancreatic tissue. After removal of the lesion the patient made an uneventful recovery and shows no signs of long-term pulmonary sequelae.
dc.relation.isversionof10.1055/s-0033-1354745
dc.rightsinfo:eu-repo/semantics/openAccess
dc.titleRecurrent Hemoptysis And A Mass In The Thorax In An Infant: The Split Notochord Syndrome
dc.typeinfo:eu-repo/semantics/article
dc.relation.journalEuropean Journal of Pediatric Surgery Reports
dc.contributor.departmentÇocuk Cerrahisi
dc.identifier.volume2
dc.identifier.issue1
dc.identifier.startpage38
dc.identifier.endpage42
dc.description.indexPubMed


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