dc.creatorFaria, MHG
dc.creatorDoria-Netto, RH
dc.creatorOsugue, GJ
dc.creatorQueiroz, LD
dc.creatorChaddad-Neto, FE
dc.date2013
dc.dateOCT
dc.date2014-07-30T13:40:59Z
dc.date2015-11-26T16:41:49Z
dc.date2014-07-30T13:40:59Z
dc.date2015-11-26T16:41:49Z
dc.date.accessioned2018-03-28T23:26:09Z
dc.date.available2018-03-28T23:26:09Z
dc.identifierNeurologia Medico-chirurgica. Japan Neurosurgical Soc, v. 53, n. 10, n. 712, n. 716, 2013.
dc.identifier0470-8105
dc.identifier1349-8029
dc.identifierWOS:000326199000010
dc.identifier10.2176/nmc.cr2012-0203
dc.identifierhttp://www.repositorio.unicamp.br/jspui/handle/REPOSIP/53571
dc.identifierhttp://repositorio.unicamp.br/jspui/handle/REPOSIP/53571
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1273057
dc.descriptionMelanotic schwannoma (MS) is an unusual variant of nerve sheath neoplasm. Only 10% of these tumors will undergo malignant degeneration, with exceedingly rare reported metastasis. We present a 32-year-old woman with a 6-month history of cervical pain and left arm progressive weakness. Neurological examination showed a left upper limb radicular pain, with pyramidal syndrome at C5 level. The magnetic resonance imaging (MRI) study highlighted an intradural extramedullary heterogeneous mass along the spinal cord at the C4-C5 level, slightly hyperintense with T-1 and hypointense with T-2-weighted sequences, invading the left neural foramen. The patient underwent C3-C5 laminectomy with total resection of a black tumor. In the postoperative period, a patent deficit of shoulder abduction ensued related to the nervous section. Microscopically, compactly fascicles of spindle-shaped cells with pleomorphic and hypercromatic nuclei, dark brown intracellular pigments, as well as some mitotic figures were seen. Immunohistochemical stains for S-100, Human Melanoma Black-45 (HME-45), and vimentin were positive, with Ki-67 Labelling Index (LI) of 15% compatible with MS. Six months after radiotherapy she presents local recurrence and lung metastatic dissemination of the MS. She underwent left pulmonary segmentectomy, followed by chemotherapy and radiosurgery. The patient developed a febrile neutropenia and worsening of general status, and died after 3 months due to respiratory complications. MS are rare tumors with potential for local recurrence and distal metastasis. Complete surgical resection remains as the treatment of choice, once the uncommon cases with malignant progression shows low response to chemo and radiotherapy.
dc.description53
dc.description10
dc.description712
dc.description716
dc.languageen
dc.publisherJapan Neurosurgical Soc
dc.publisherTokyo
dc.publisherJapão
dc.relationNeurologia Medico-chirurgica
dc.relationNeurol. Med.-Chir.
dc.rightsfechado
dc.sourceWeb of Science
dc.subjectcervical neoplasm
dc.subjectmelanotic schwannoma
dc.subjectmetastasis
dc.subjectnerve sheath tumor
dc.subjectspine
dc.subjectOf-the-literature
dc.subjectMelanocytic Schwannoma
dc.subjectLesions
dc.subjectGene
dc.titleMelanotic Schwannoma of the Cervical Spine Progressing With Pulmonary Metastasis: Case Report
dc.typeArtículos de revistas


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