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"documento" => "article" "crossmark" => 0 "subdocumento" => "sco" "cita" => "Acta Otorrinolaringol Esp. 2011;62:465-8" "abierto" => array:3 [ "ES" => true "ES2" => true "LATM" => true ] "gratuito" => true "lecturas" => array:2 [ "total" => 2135 "formatos" => array:3 [ "EPUB" => 40 "HTML" => 1457 "PDF" => 638 ] ] "en" => array:13 [ "idiomaDefecto" => true "cabecera" => "<span class="elsevierStyleTextfn">Case study</span>" "titulo" => "Sensorineural Hearing Loss Evolution in Vogt–Koyanagi–Harada Syndrome" "tienePdf" => "en" "tieneTextoCompleto" => "en" "tieneResumen" => array:2 [ 0 => "en" 1 => "es" ] "paginas" => array:1 [ 0 => array:2 [ "paginaInicial" => "465" "paginaFinal" => "468" ] ] "titulosAlternativos" => array:1 [ "es" => array:1 [ "titulo" => "Evolución de la hipoacusia neurosensorial bilateral en el síndrome de Vogt Koyanagi Harada" ] ] "contieneResumen" => array:2 [ "en" => true "es" => true ] "contieneTextoCompleto" => array:1 [ "en" => true ] "contienePdf" => array:1 [ "en" => true ] "resumenGrafico" => array:2 [ "original" => 0 "multimedia" => array:7 [ "identificador" => "fig0005" "etiqueta" => "Figure 1" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr1.jpeg" "Alto" => 2424 "Ancho" => 3285 "Tamanyo" => 359069 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0015" class="elsevierStyleSimplePara elsevierViewall">Changes in macular width and hearing over time. <span class="elsevierStyleItalic">X</span>-axis: time in months, from April 2008 until November 2009, with the treatments applied. <span class="elsevierStyleItalic">Y</span>-axis: macular width in microns. <span class="elsevierStyleItalic">Z</span>-axis: hearing in dB. Solid lines express the variation of macular width over time: marked with squares for the right eye and with diamonds for the left eye. 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It is possible to identify the posterior side of the digastric muscle (md) and the pointer (p).</p>" ] ] ] "textoCompleto" => "<span class="elsevierStyleSections"><span id="sec0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Introduction</span><p id="par0005" class="elsevierStylePara elsevierViewall">Facial nerve schwannomas are infrequent benign tumours.<a class="elsevierStyleCrossRefs" href="#bib0005"><span class="elsevierStyleSup">1,2</span></a> They are characterised by progressive facial palsy symptoms when they affect the intratemporal facial nerve. In contrast, the first symptom manifested by extratemporal schwannomas is a parotid mass, which can be mistaken for a parotid tumour.<a class="elsevierStyleCrossRefs" href="#bib0015"><span class="elsevierStyleSup">3,4</span></a> Preoperative diagnosis is difficult,<a class="elsevierStyleCrossRefs" href="#bib0025"><span class="elsevierStyleSup">5,6</span></a> so different therapeutic algorithms have been proposed to indicate the course of action in case of intraoperative suspicion of facial nerve schwannoma.<a class="elsevierStyleCrossRefs" href="#bib0015"><span class="elsevierStyleSup">3,4,7</span></a></p></span><span id="sec0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Clinical Case</span><span id="sec0015" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Clinical Case 1</span><p id="par0010" class="elsevierStylePara elsevierViewall">We present the case of a 51-year-old female patient who attended consultation due to a painless right submandibular nodule of 4 months’ evolution, with fine needle aspiration (FNA) cytology suggestive of pleomorphic adenoma and with no other clinical manifestations. The preoperative magnetic resonance imaging (MRI) study revealed another, previously unknown injury in the deep plane of the left parotid gland, also suggestive of pleomorphic adenoma. For this reason, the patient was taken to surgery with the tentative diagnosis of pleomorphic adenoma of the right submandibular and left parotid glands. The parotidectomy found a tumour in the anterior region of the stylomastoid foramen (<a class="elsevierStyleCrossRef" href="#fig0005">Fig. 1</a>). The facial nerve entered the tumour and could not be separated from it, so an intraoperative biopsy had to be performed. The study was consistent with schwannoma, so the tumour was dissected, attempting to preserve the majority of nerve fibres. The patient presented a House-Brackmann grade V facial palsy in the immediate postoperative period. Facial function improved after rehabilitation treatment, achieving almost complete eye closure and facial mobility in lower areas. She did not require reoperation in 2 years of follow-up.</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia></span><span id="sec0020" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Clinical Case 2</span><p id="par0015" class="elsevierStylePara elsevierViewall">We also present the case of a 52-year-old male patient who complained of a painless lump in the right parotid region of 3 months’ evolution, with no other clinical manifestations. The FNA cytology was suggestive of pleomorphic adenoma. The MRI showed a 4-cm mass in the right parotid, suggestive of pleomorphic adenoma (<a class="elsevierStyleCrossRef" href="#fig0010">Fig. 2</a>). We decided to perform a subtotal parotidectomy. During surgery, we could not identify the facial nerve trunk so we began to search for it through retrograde dissection. Once we reached the fork, we observed that the nerve entered the tumour without the possibility of separating them. Although an intraoperative biopsy was consistent with pleomorphic adenoma, given the strong suspicion that this was a schwannoma, we decided to excise the tumour to preserve the nerve fibres. The definitive result of the histological study was schwannoma with a microscopic epithelioid pattern. The patient presented transient facial paresis with complete recovery of facial function 3 months after surgery. He did not require reoperation after 16 months of follow-up.</p><elsevierMultimedia ident="fig0010"></elsevierMultimedia></span></span><span id="sec0025" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Discussion</span><p id="par0020" class="elsevierStylePara elsevierViewall">Facial nerve schwannomas are infrequent benign tumours.<a class="elsevierStyleCrossRefs" href="#bib0005"><span class="elsevierStyleSup">1,8</span></a> Intraparotid involvement is the least common,<a class="elsevierStyleCrossRefs" href="#bib0005"><span class="elsevierStyleSup">1,4,7,9</span></a> representing approximately 10% of all cases of facial nerve schwannomas.<a class="elsevierStyleCrossRefs" href="#bib0050"><span class="elsevierStyleSup">10,11</span></a> Its malignant degeneration is not frequent.<a class="elsevierStyleCrossRef" href="#bib0010"><span class="elsevierStyleSup">2</span></a></p><p id="par0025" class="elsevierStylePara elsevierViewall">The extratemporal form commonly manifests as a painless parotid mass with slow growth<a class="elsevierStyleCrossRefs" href="#bib0015"><span class="elsevierStyleSup">3,4,8,11</span></a> and unaffected facial nerve function.<a class="elsevierStyleCrossRefs" href="#bib0010"><span class="elsevierStyleSup">2,4,5,7,8,11</span></a> These clinical features are similar to those of pleomorphic adenoma.<a class="elsevierStyleCrossRefs" href="#bib0020"><span class="elsevierStyleSup">4,8,10</span></a> Our first case of facial schwannoma was detected accidentally during the magnetic resonance imaging study of a submandibular gland tumour, while the second patient presented the typical clinical symptoms.</p><p id="par0030" class="elsevierStylePara elsevierViewall">Preoperative diagnosis is difficult<a class="elsevierStyleCrossRefs" href="#bib0020"><span class="elsevierStyleSup">4–6,12</span></a> because FNA cytology and MRI studies are not always conclusive.<a class="elsevierStyleCrossRefs" href="#bib0050"><span class="elsevierStyleSup">10,13</span></a> The lack of a preoperative diagnosis means that the surgeon may have to change the surgical plan based on intraoperative findings and have to decide what to do with a tumour that affects the facial nerve and whose resection may lead to considerable morbidity.<a class="elsevierStyleCrossRef" href="#bib0050"><span class="elsevierStyleSup">10</span></a> Different authors have proposed various algorithms to facilitate intraoperative treatment decisions.<a class="elsevierStyleCrossRefs" href="#bib0015"><span class="elsevierStyleSup">3,4,7</span></a> Suspicion that the tumour found is a facial schwannoma is established through difficulty in identifying the facial nerve,<a class="elsevierStyleCrossRefs" href="#bib0035"><span class="elsevierStyleSup">7,11</span></a> strong adhesion between the nerve and the tumour<a class="elsevierStyleCrossRefs" href="#bib0025"><span class="elsevierStyleSup">5,11</span></a> and the presence of facial muscle activity by electrical stimulation of the tumour.<a class="elsevierStyleCrossRefs" href="#bib0025"><span class="elsevierStyleSup">5,7,8</span></a> Alicandri-Ciufelli et al.<a class="elsevierStyleCrossRef" href="#bib0035"><span class="elsevierStyleSup">7</span></a> recommend performing an intraoperative biopsy for diagnostic purposes if the tumour cannot be resected without damaging the nerve at its trunk or fork and the patient presents good facial nerve function (House-Brackmann grade III or less).</p><p id="par0035" class="elsevierStylePara elsevierViewall">Intraoperative biopsy has also been recommended to rule out malignancy,<a class="elsevierStyleCrossRefs" href="#bib0005"><span class="elsevierStyleSup">1,4,10,12,14</span></a> but we must consider that the intraoperative diagnosis is not always correct.<a class="elsevierStyleCrossRefs" href="#bib0020"><span class="elsevierStyleSup">4,14</span></a> In the second case presented here, the preoperative biopsy was consistent with pleomorphic adenoma. However, faced with a strong suspicion of schwannoma, excision was not performed and tumour dissection was chosen instead. Subsequently, the definitive histological study confirmed the diagnosis of schwannoma.</p><p id="par0040" class="elsevierStylePara elsevierViewall">Some authors suggest that the best approach for patients with normal facial nerve function or mild dysfunction would be therapeutic abstention (not carrying out the excision), considering the suboptimal results obtained with nerve reconstruction.<a class="elsevierStyleCrossRefs" href="#bib0020"><span class="elsevierStyleSup">4,11</span></a> Alicandri-Ciufelli et al.<a class="elsevierStyleCrossRef" href="#bib0035"><span class="elsevierStyleSup">7</span></a> propose an intraoperative action guide for intraparotid facial nerve schwannomas, based on the classification by Marchioni et al.<a class="elsevierStyleCrossRef" href="#bib0010"><span class="elsevierStyleSup">2</span></a> This classification relates the position of the tumour within the facial nerve path with the possibility of injuring the nerve when resecting the tumour. It divides schwannomas into 4 types. Type A includes tumours that can be resected without sacrificing the facial nerve and that may be located in any portion of the extratemporal pathway. Type B includes tumours that can be resected with a partial sacrifice of facial function because they involve one of the peripheral branches or their distal divisions. Type C includes tumours that require sacrificing the main trunk of the nerve for their resection, while type D includes tumours that require sacrificing the trunk and its main divisions to be resected. Alicandri-Ciufelli et al.<a class="elsevierStyleCrossRef" href="#bib0035"><span class="elsevierStyleSup">7</span></a> propose that type A schwannomas should be resected regardless of preoperative facial function. For type B schwannomas, they propose resecting those affecting a branch of the facial nerve whose sacrifice does not cause significant facial nerve dysfunction. With regard to type C and D schwannomas, they recommend resecting tumours that cause facial paralysis of House-Brackmann grade IV or greater. For cases, which cause a facial nerve dysfunction of House-Brackmann grade III or less, they do not recommend resecting the tumours in which malignancy has been ruled out through a preoperative biopsy. Once resection of the schwannoma has been decided against, some authors advocate draining the tumour and controlling its evolution.<a class="elsevierStyleCrossRef" href="#bib0075"><span class="elsevierStyleSup">15</span></a></p><p id="par0045" class="elsevierStylePara elsevierViewall">Our cases followed the recommended annual monitoring.<a class="elsevierStyleCrossRef" href="#bib0055"><span class="elsevierStyleSup">11</span></a> Given the characteristic slow growth of schwannomas, a period of prolonged absence of facial paralysis is expected.</p></span><span id="sec0030" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Conflict of interests</span><p id="par0050" class="elsevierStylePara elsevierViewall">The authors have no conflicts of interest to declare.</p></span></span>" "textoCompletoSecciones" => array:1 [ "secciones" => array:9 [ 0 => array:2 [ "identificador" => "xres94892" "titulo" => "Abstract" ] 1 => array:2 [ "identificador" => "xpalclavsec82045" "titulo" => "Keywords" ] 2 => array:2 [ "identificador" => "xres94893" "titulo" => "Resumen" ] 3 => array:2 [ "identificador" => "xpalclavsec82044" "titulo" => "Palabras clave" ] 4 => array:2 [ "identificador" => "sec0005" "titulo" => "Introduction" ] 5 => array:3 [ "identificador" => "sec0010" "titulo" => "Clinical Case" "secciones" => array:2 [ 0 => array:2 [ "identificador" => "sec0015" "titulo" => "Clinical Case 1" ] 1 => array:2 [ "identificador" => "sec0020" "titulo" => "Clinical Case 2" ] ] ] 6 => array:2 [ "identificador" => "sec0025" "titulo" => "Discussion" ] 7 => array:2 [ "identificador" => "sec0030" "titulo" => "Conflict of interests" ] 8 => array:1 [ "titulo" => "References" ] ] ] "pdfFichero" => "main.pdf" "tienePdf" => true "fechaRecibido" => "2010-05-02" "fechaAceptado" => "2010-09-20" "PalabrasClave" => array:2 [ "en" => array:1 [ 0 => array:4 [ "clase" => "keyword" "titulo" => "Keywords" "identificador" => "xpalclavsec82045" "palabras" => array:3 [ 0 => "Schwannoma" 1 => "Facial nerve" 2 => "Parotid gland" ] ] ] "es" => array:1 [ 0 => array:4 [ "clase" => "keyword" "titulo" => "Palabras clave" "identificador" => "xpalclavsec82044" "palabras" => array:3 [ 0 => "Schwannoma" 1 => "Nervio facial" 2 => "Glándula parótida" ] ] ] ] "tieneResumen" => true "resumen" => array:2 [ "en" => array:2 [ "titulo" => "Abstract" "resumen" => "<p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">Intraparotid facial nerve schwannomas are rare, their preoperative diagnosis is difficult, and there are controversies about how to proceed when they are suspected intraoperatively. We present two cases of intraparotid facial nerve schwannoma that were diagnosed during parotid surgery, and describe the procedure and follow-up performed.</p>" ] "es" => array:2 [ "titulo" => "Resumen" "resumen" => "<p id="spar0010" class="elsevierStyleSimplePara elsevierViewall">La localización intraparotídea de schwannomas del nervio facial es poco frecuente y su diagnóstico preoperatorio es difícil. Estos hechos causan controversia sobre cual es la actitud que debe seguirse ante la sospecha intraoperatoria de un schwannoma del nervio facial intraparotídeo. Se presentan dos casos de schwannoma intraparotídeo del nervio facial diagnosticados en el transcurso de una cirugía de parótida. Se describe la conducta terapéutica y seguimiento realizado en ambos casos.</p>" ] ] "NotaPie" => array:1 [ 0 => array:2 [ "etiqueta" => "☆" "nota" => "<p class="elsevierStyleNotepara">Please cite this article as: Villatoro JC, et al. Dos casos de schwannoma intraparotídeo del nervio facial. Acta Otorrinolaringol Esp. 2011;62:469–71.</p>" ] ] "multimedia" => array:2 [ 0 => array:7 [ "identificador" => "fig0005" "etiqueta" => "Figure 1" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr1.jpeg" "Alto" => 1188 "Ancho" => 1565 "Tamanyo" => 377307 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0015" class="elsevierStyleSimplePara elsevierViewall">Tumour (s) located in the region anterior to the stylomastoid foramen, showing branches of the facial nerve (f). It is possible to identify the posterior side of the digastric muscle (md) and the pointer (p).</p>" ] ] 1 => array:7 [ "identificador" => "fig0010" "etiqueta" => "Figure 2" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr2.jpeg" "Alto" => 1277 "Ancho" => 1574 "Tamanyo" => 178973 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0020" class="elsevierStyleSimplePara elsevierViewall">Magnetic resonance image in T2 showing the tumour (arrow) located in the right parotid gland, with a heterogeneous pattern.</p>" ] ] ] "bibliografia" => array:2 [ "titulo" => "References" "seccion" => array:1 [ 0 => array:2 [ "identificador" => "bibs0005" "bibliografiaReferencia" => array:15 [ 0 => array:3 [ "identificador" => "bib0005" "etiqueta" => "1" "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "Intraparotid facial nerve schwannoma in a child" "autores" => array:1 [ 0 => array:2 [ "etal" => false "autores" => array:4 [ 0 => "B.N. 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