Müllerian papilloma of the rectovaginal septum
Clínica/ presentation of a fifty-one year old fema/e patient who carried Müller's papilloma inrectovaginal septum.These tumors are rare and their origin isembryologic; they are the remains ofparamesonephrical or ducts of Mül/er fusion fromwhich deve/op the uterus and the upper sector ofvagina.They a...
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| Andere auteurs: | , , , , |
| Formaat: | article |
| Taal: | Spaans |
| Gepubliceerd in: |
2005
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| Onderwerpen: | |
| Online toegang: | https://revista.scu.org.uy/index.php/cir_urug/article/view/4587 |
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| Samenvatting: | Clínica/ presentation of a fifty-one year old fema/e patient who carried Müller's papilloma inrectovaginal septum.These tumors are rare and their origin isembryologic; they are the remains ofparamesonephrical or ducts of Mül/er fusion fromwhich deve/op the uterus and the upper sector ofvagina.They are frequent in girls, exceptional in adultsand they appear as genitorrhage or tumoration ofthe vaginal sac fundus; very rarely do they producestraining or rectal tenesmus.They are benign tumors having p/eomorphicmorpho/ogy, with a we/1 defined histologic and immunohistochemicalprofile and /ow possibility ofturning ma/ignant.Their clinical presentation with rectal syndromeelements, the exceptional nature of this type of lesion, its uncertain diagnosis and the surgica/ tacticsadopted, confer interest to this communication. |
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