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Pseudomyogenic hemangioendothelioma: a little-known tumor

dc.contributor.authorSantos, RP
dc.contributor.authorCarvalho, S
dc.contributor.authorJoana, G
dc.contributor.authorPerdal, J
dc.date.accessioned2019-01-18T12:45:30Z
dc.date.available2019-01-18T12:45:30Z
dc.date.issued2018-12
dc.description.abstractPseudomyogenic hemangioendothelioma (PHE) is a rare indolent vascular tumor that typically has a multifocal presentation and involves multiple tissue planes. This report describes a 34-year-old man with multiple infiltrated brown papules and plaques on his left leg that had evolved for 6 months. The skin biopsy revealed a dermal and subcutaneous neoplasm composed of fascicles of spindle cells with atypia and epithelioid cells with prominent nucleoli and abundant eosinophilic cytoplasm. There was no evidence of necrosis, and the mitotic rate was low. There was strong reactivity with cytokeratin AE1/AE3, ERG, and FLI1, multifocal reactivity with smooth muscle actin, and focal reactivity with CD31. There was no expression of keratin MNF116, CAM5.2, CD34, CAMTA1, S100-protein, epithelial membrane antigen, melan-A, HMB-45, factor XIIIa, HHV8, or CD10. The nuclei of neoplastic cells showed intact expression of INI1. The clinical, histological, and immunophenotypical aspects were consistent with a diagnosis of PHE. A lower limb CT scan showed lesions in the skin, muscle, and bone planes. The patient was sent to an oncology center, where he maintains regular clinical and imagiological follow-up.pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.citationActa Dermatovenerol Alp Pannonica Adriat. 2018 Dec;27(4):225-229.pt_PT
dc.identifier.urihttp://hdl.handle.net/10400.23/1300
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.subjectHemangioendoteliomapt_PT
dc.subjectNeoplasias de Tecidos Molespt_PT
dc.titlePseudomyogenic hemangioendothelioma: a little-known tumorpt_PT
dc.typejournal article
dspace.entity.typePublication
oaire.citation.issue4pt_PT
oaire.citation.startPage225-229pt_PT
oaire.citation.volume27pt_PT
rcaap.rightsopenAccesspt_PT
rcaap.typearticlept_PT

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