Please use this identifier to cite or link to this item: https://olympias.lib.uoi.gr/jspui/handle/123456789/18026
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dc.contributor.authorThiry, A. J.en
dc.contributor.authorGiannakopoulos, X.en
dc.date.accessioned2015-11-24T18:50:01Z-
dc.date.available2015-11-24T18:50:01Z-
dc.identifier.issn0248-0018-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/18026-
dc.rightsDefault Licence-
dc.subjectAdulten
dc.subjectDigestive System Diseases/etiologyen
dc.subjectHumansen
dc.subjectMaleen
dc.subjectNeurilemmoma/complications/*diagnosisen
dc.subjectRetroperitoneal Neoplasms/complications/*diagnosisen
dc.subjectUrologic Diseases/etiologyen
dc.titleSub-peritoneal schwannomaen
heal.typejournalArticle-
heal.type.enJournal articleen
heal.type.elΆρθρο Περιοδικούel
heal.identifier.secondaryhttp://www.ncbi.nlm.nih.gov/pubmed/7400602-
heal.languagefr-
heal.accesscampus-
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Επιστημών Υγείας. Τμήμα Ιατρικήςel
heal.publicationDate1980-
heal.abstractThe authors report a rare case of sub-peritoneal malignant schwannoma developing 5 years after excision of a schwannoma of the sigmoid. The non-excised tumour compressed the bladder and one ureter. This type of tumour, extremely rare, accounts for less than 2% of tumours. Arising in the cells of the Schwann sheath, and as a general rule developing in the central nervous system, peripheral nerves of the neck, mediastinum, flexor surfaces of the extremities or nerves of the digestive tract, they may be benign tumours do not recur. The example reported here showed that this distinction is in no way absolute.en
heal.journalNameJ Urol (Paris)en
heal.journalTypepeer-reviewed-
heal.fullTextAvailabilityTRUE-
Appears in Collections:Άρθρα σε επιστημονικά περιοδικά ( Ανοικτά) - ΙΑΤ

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