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Disseminated Peritoneal Leiomyomatosis: A Rare Case Report in a Woman without a Prior History of Uterine Leiomyomas

dc.contributor.authorLameiras Costa, MD
dc.contributor.authorCunha, TM
dc.date.accessioned2022-08-10T13:32:22Z
dc.date.available2022-08-10T13:32:22Z
dc.date.issued2020
dc.description.abstractDisseminated peritoneal leiomyomatosis (DPL) is a rare disease characterized by multiple leiomyomas disseminated throughout the peritoneal cavity, occurring most commonly in women of childbearing age. Although typically benign, DPL may degenerate into malignancy. As the majority are asymptomatic, these tumors are usually incidentally found incidentally. Differential diagnosis includes peritoneal carcinomatosis peritoneal or abdominal disseminated malignancy; the clinical and radiological context can help differentiate these entities, but only histopathological examination achieves the final diagnosis. The authors present a case of a woman with DPL found during infertility workup. She had undergone laparoscopic broad ligament myomectomy 5 years previously, but there was no prior history of uterine leiomyomas. A revision of the clinical, pathological and imaging features of this entity was also performed.pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.citationActa Radiol Port. 2020; 32(2)27-30pt_PT
dc.identifier.urihttp://hdl.handle.net/10400.17/4195
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.publisherSociedade Portuguesa de Radiologia e Medicina Nuclearpt_PT
dc.subjectDisseminated peritoneal leiomyomatosispt_PT
dc.subjectLeiomyomapt_PT
dc.subjectCase Reportpt_PT
dc.subjectHCC IMApt_PT
dc.titleDisseminated Peritoneal Leiomyomatosis: A Rare Case Report in a Woman without a Prior History of Uterine Leiomyomaspt_PT
dc.title.alternativeLeiomiomatose Peritoneal Disseminada: Relato de um Caso Raro numa Mulher sem História Prévia de Leiomiomas Uterinospt_PT
dc.typejournal article
dspace.entity.typePublication
oaire.citation.endPage30pt_PT
oaire.citation.issue2pt_PT
oaire.citation.startPage27pt_PT
oaire.citation.volume32pt_PT
rcaap.rightsopenAccesspt_PT
rcaap.typearticlept_PT

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