dc.creatorWortsman, Ximena
dc.creatorLobos, Nelson
dc.creatorDe La Parra, Rodrigo
dc.creatorCarreno, Laura
dc.date.accessioned2019-03-18T11:53:08Z
dc.date.available2019-03-18T11:53:08Z
dc.date.created2019-03-18T11:53:08Z
dc.date.issued2015
dc.identifierIndian Journal of Dermatology, Volumen 60, Issue 4, 2018,
dc.identifier19983611
dc.identifier00195154
dc.identifier10.4103/0019-5154.160522
dc.identifierhttps://repositorio.uchile.cl/handle/2250/166606
dc.description.abstractActive bleeding in plexiform neurofibromatosis can be a life-threatening complication in neurofibromatosis type 1 (NF1). The prompt imaging support of 2D-3D ultrasound (US) and computed tomography (CT) during the active hemorrhage phase of cutaneous neurofibromas has not been previously reported. We report a case with NF1 who experienced a sudden swelling in the parieto-temporal region that corresponded to a massive and active hemorrhage within a plexiform neurofibroma. The US and CT imaging characteristics of this bleeding tumor are shown. Active hemorrhage in a plexiform neurofibroma of the scalp appeared in US as a heterogeneous hypodermal mass. CT demonstrated a fully hyperdense soft tissue mass. These characteristics differ from the non-complicated or old hemorrhagic imaging appearances of scalp plexiform neurofibromas and encourage prompt surgical treatment. This case report demonstrates the usefulness of imaging support in the early diagnosis of this hemorrhagic complication of
dc.languageen
dc.publisherMedknow Publications
dc.rightshttp://creativecommons.org/licenses/by-nc-nd/3.0/cl/
dc.rightsAttribution-NonCommercial-NoDerivs 3.0 Chile
dc.sourceIndian Journal of Dermatology
dc.subjectHemorrhagic neurofibromatosis
dc.subjectneurofibromatosis
dc.subjectneurofibromatosis computed tomography
dc.subjectneurofibromatosis imaging
dc.subjectneurofibromatosis ultrasound
dc.subjectscalp ultrasound
dc.subjectskin ultrasound
dc.titleMultidimensional ultrasound and computed tomography imaging support in bleeding plexiform neurofibromatosis of the scalp: A case report and literature review
dc.typeArtículos de revistas


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