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Sirolimus in the Treatment of Cystic Lymphangioma in a Pediatric Patient

dc.contributor.authorFidalgo Martins, I
dc.contributor.authorCordeiro, AI
dc.contributor.authorPaiva Lopes, MJ
dc.date.accessioned2023-02-10T11:49:20Z
dc.date.available2023-02-10T11:49:20Z
dc.date.issued2022
dc.description.abstractCystic lymphangioma (CL) is a rare benign tumor, which occurs typically during childhood, with craniofacial, cervical or axillary being the most common locations. Lymphangiomas management can be challenging due to their permeative growth throughout tissue layers. Sirolimus is an immunosuppressive and antitumor agent that can inhibit abnormal vascular proliferation by blocking the mTOR/PI3K pathway. It is typically well-tolerated, with nausea, cytopenias, and metabolic imbalances as the most significant adverse effects. We present the case of a pediatric patient in which sirolimus was used to treat a macrocytic lymphangioma, highlighting its effectiveness and safety.pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.citationPort J Dermatol and Venereol. 2022;80(3):227-230pt_PT
dc.identifier.urihttp://hdl.handle.net/10400.17/4396
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.publisherSociedade Portuguesa de Dermatologiapt_PT
dc.subjectLymphangiomapt_PT
dc.subjectSirolimuspt_PT
dc.subjectChildpt_PT
dc.subjectCase Reportpt_PT
dc.subjectHDE PEDpt_PT
dc.titleSirolimus in the Treatment of Cystic Lymphangioma in a Pediatric Patientpt_PT
dc.title.alternativeSirolimus no Tratamento de um Linfangioma Quístico num Doente Pediátricopt_PT
dc.typejournal article
dspace.entity.typePublication
oaire.citation.endPage230pt_PT
oaire.citation.issue3pt_PT
oaire.citation.startPage227pt_PT
oaire.citation.volume80pt_PT
rcaap.rightsopenAccesspt_PT
rcaap.typearticlept_PT

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