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Diagnostic difficulties in congenital tumor with positive antibodies for skeletal muscle. Lipofibromatosis case report

dc.contributor.authorCaƱon-Cubillos Oriana
dc.contributor.authorUribe-Lopez, Juan Manuel
dc.contributor.authorFranco-Olaya, Mariana
dc.contributor.authorMendez-Reyes, Hector F.
dc.contributor.authorVelasquez-Portilla, Mauricio
dc.contributor.authorOlaya-C., Mercedes
dc.contributor.authorMessa Botero, Oscar Alberto
dc.contributor.corporatenamePontificia Universidad Javeriana. Facultad de Medicina. Departamento de PatologĆ­aspa
dc.contributor.javerianateacherOlaya-C., Mercedes
dc.contributor.javerianateacherMessa Botero, Oscar Alberto
dc.date.accessioned2023-03-14T15:10:36Z
dc.date.available2023-03-14T15:10:36Z
dc.date.created2022-08-08
dc.description.abstractenglishIntroduction: Congenital soft tissue tumors are uncommon; proper diagnosis calls for histopathological experience and ancillary techniques based upon immunohistochemial, cytogenetic, and molecular biology. Following excision, intermediately aggressive soft tumors tend to local recurrence, which significantly impacts prognosis; some cases occur close to malignity; subsequently, diagnostic implications are enormous for the patient. Case report: A 26-day old neonate with a posterior left thigh mass entered hospital. Initial biopsy analysis could not rule out either striated muscle origin or malignancy; resection and classification of surgical piece followed. Pursuant to resection, using immunohistochemistry panel, tumor analysis and classification took place. Conclusion: Soft tumor diagnosis is a complex process, even more so for newborns. Infrequent occurrence requires that examiners have ample histopathological experience in the handling of ancillary techniques. Furthermore, as in lipofibromatosis, determining the presence of trapped vs. malignant tissue hinders proper classification, which, in turn, has profound implications for the patient. We include a standard diagnostic algorithm based on clinical and histological characteristics for this type of congenital lesions.spa
dc.description.comunidadNeonatos con Tumores congƩnitos de partes blandasspa
dc.description.esciNospa
dc.description.indexingRevista Internacional - No indexadaspa
dc.description.orcidhttps://orcid.org/0000-0003-3507-7596spa
dc.description.orcidhttps://orcid.org/0000-0001-8932-4877spa
dc.description.orcidhttps://orcid.org/0000-0002-7147-425Xspa
dc.description.orcidhttps://orcid.org/0000-0001-7982-4552spa
dc.formatPDFspa
dc.format.mimetypeapplication/pdfspa
dc.identifierhttp://www.jclinmedsurgery.com/articles.php#spa
dc.identifier.instnameinstname:Pontificia Universidad Javerianaspa
dc.identifier.issn2833-5465spa
dc.identifier.reponamereponame:Repositorio Institucional - Pontificia Universidad Javerianaspa
dc.identifier.repourlrepourl:https://repository.javeriana.edu.cospa
dc.identifier.urihttp://hdl.handle.net/10554/63761
dc.language.isoengspa
dc.relation.citationendpage5spa
dc.relation.citationissue2spa
dc.relation.citationstartpage1spa
dc.relation.citationvolume2spa
dc.relation.ispartofjournalJournal of Clinical and Medical Surgeryspa
dc.rights.coarhttp://purl.org/coar/access_right/c_abf2spa
dc.rights.licenceAtribución-NoComercial 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/*
dc.subject.keywordCongenital Tumorspa
dc.subject.keywordFibroblastic/ Myofibroblastic Tumorspa
dc.subject.keywordLipofibromatosisspa
dc.subject.keywordPediatric Pathologyspa
dc.titleDiagnostic difficulties in congenital tumor with positive antibodies for skeletal muscle. Lipofibromatosis case reportspa
dc.type.coarhttp://purl.org/coar/resource_type/c_93fcspa
dc.type.hasversionhttp://purl.org/coar/version/c_ab4af688f83e57aa
dc.type.localArtĆ­culo de revistaspa

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