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          "en" => "<p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">&#40;A&#41; An area of bronchial epithelium can be seen on lower magnification &#40;top right&#44; darker area&#41;&#46; The rest of the sample consists of tumor tissue&#46; &#40;B&#41; Fusiform cells and granular cytoplasma can been seen on greater magnification&#46; Bronchial schwannoma or granular cell tumor&#46; &#40;C&#41; Immunohistochemistry positive for S100 &#40;darker staining&#41;&#46;</p>"
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Four weeks later&#44; a radiological control was performed and the patient was referred to the respiratory medicine department&#46; During anamnesis&#44; she reported a long history of episodes of lower respiratory tract infections&#46; Physical examination and blood test results were normal&#46; Chest X-ray showed LUL atelectasis with left hilar elevation&#46; Chest computed tomography revealed a 2<span class="elsevierStyleHsp" style=""></span>cm nodular lesion in the LUL&#44; causing partial atelectasis&#44; with no mediastinal or hilar lymphadenopathies&#46; Spirometric results were normal&#46; Fiberoptic bronchoscopy showed a pedunculated lesion in the left bronchial tree&#44; obstructing the upper lobe&#46; The lesion surface was smooth&#44; shiny and vascularized&#46; It was contingent on the carina dividing the lobes&#44; and there was no adhesion to the lateral walls&#46; Biopsy showed fusiform&#44; polygonal cells and granular cytoplasm with immunohistochemical &#40;IHC&#41; expression of neuron-specific enolase&#44; S100 protein and vimentin &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Fig&#46; 1</a>&#41;&#44; indicative of LUL schwannoma&#46;</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia><p id="par0015" class="elsevierStylePara elsevierViewall">The LUL was lobectomized&#44; and the patient did not require any further treatment&#46;</p><p id="par0020" class="elsevierStylePara elsevierViewall">Schwannomas are extremely rare<a class="elsevierStyleCrossRef" href="#bib0030"><span class="elsevierStyleSup">1</span></a> benign tumors&#44; originating in the Schwann cells that produce the myelin sheath of the peripheral nerves&#46; The first case was described by Feckner in 1938&#44; and at least 80 cases have been published since then&#46; These are slow-growing tumors&#44; that do not infiltrate the neuronal axon&#44; but which can affect nerve conduction by extrinsic compression&#46; They appear in wide range of sites&#44; the most common of which are the skin and the tongue&#46;<a class="elsevierStyleCrossRef" href="#bib0035"><span class="elsevierStyleSup">2</span></a> Endobronchial presentation occurs in only 6&#37; of cases&#46;<a class="elsevierStyleCrossRefs" href="#bib0035"><span class="elsevierStyleSup">2&#44;3</span></a></p><p id="par0025" class="elsevierStylePara elsevierViewall">Schwannomas generally occur in middle age&#44; and no differences are observed between sexes&#46;<a class="elsevierStyleCrossRef" href="#bib0030"><span class="elsevierStyleSup">1</span></a> Clinical presentation can very&#44; and is determined by the size and location&#46; Early symptoms include asthma&#44; unproductive cough&#44; recurrent infections &#40;as in our case&#41;&#44; fever&#44; dyspnea and hemoptysis&#46;<a class="elsevierStyleCrossRefs" href="#bib0035"><span class="elsevierStyleSup">2&#44;3</span></a> Lesions tend to develop in the large bronchi or in bifurcatons&#46;<a class="elsevierStyleCrossRefs" href="#bib0040"><span class="elsevierStyleSup">3&#44;4</span></a> Up to 25&#37; may be multiple&#44; and they can even mimic metastasis&#44; if they occur concomitantly with other neoplasms&#46;<a class="elsevierStyleCrossRef" href="#bib0035"><span class="elsevierStyleSup">2</span></a> Radiographs can be useful in differential diagnosis&#44; but definitive diagnosis is usually obtained on fiberoptic bronchoscopy for atelectasis and secondary pneumonia&#44; as in our case&#46;<a class="elsevierStyleCrossRefs" href="#bib0035"><span class="elsevierStyleSup">2&#44;3</span></a></p><p id="par0030" class="elsevierStylePara elsevierViewall">On histological examination&#44; tumor cells are polygonal and fusiform&#44; with granular cytoplasma&#46; On IHC&#44; antigen expression is positive for S100 protein&#44; vimentin&#44; neuron-specific enolase&#44; and negative for keratins&#46;<a class="elsevierStyleCrossRef" href="#bib0045"><span class="elsevierStyleSup">4</span></a></p><p id="par0035" class="elsevierStylePara elsevierViewall">While endoscopic resection has been recommended for treating small lesions&#44; surgical resection is still the treatment of choice due to the risk of recurrence&#44; irrespective of tumor size&#46;<a class="elsevierStyleCrossRefs" href="#bib0040"><span class="elsevierStyleSup">3&#44;5</span></a> Prognosis is favorable&#44; and mean survival after surgery is longer than 5 years&#46;<a class="elsevierStyleCrossRef" href="#bib0030"><span class="elsevierStyleSup">1</span></a></p><span id="sec0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0005">Conflict of Interests</span><p id="par0040" class="elsevierStylePara elsevierViewall">The authors state that they have no conflict of interests&#46;</p></span></span>"
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Letter to the Editor
Bronchial Schwannoma: An Uncommon Tumor
Schwannoma bronquial, un tumor poco frecuente
Pedro Landete, Eusebi Chiner
Corresponding author
echinervives@gmail.com

Corresponding author.
, José Norberto Sancho-Chust, Patricia Pérez-Ferrer
Servicio de Neumología, Hospital Universitario San Juan de Alicante, San Juan, Alicante, Spain
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Four weeks later&#44; a radiological control was performed and the patient was referred to the respiratory medicine department&#46; During anamnesis&#44; she reported a long history of episodes of lower respiratory tract infections&#46; Physical examination and blood test results were normal&#46; Chest X-ray showed LUL atelectasis with left hilar elevation&#46; Chest computed tomography revealed a 2<span class="elsevierStyleHsp" style=""></span>cm nodular lesion in the LUL&#44; causing partial atelectasis&#44; with no mediastinal or hilar lymphadenopathies&#46; Spirometric results were normal&#46; Fiberoptic bronchoscopy showed a pedunculated lesion in the left bronchial tree&#44; obstructing the upper lobe&#46; The lesion surface was smooth&#44; shiny and vascularized&#46; It was contingent on the carina dividing the lobes&#44; and there was no adhesion to the lateral walls&#46; Biopsy showed fusiform&#44; polygonal cells and granular cytoplasm with immunohistochemical &#40;IHC&#41; expression of neuron-specific enolase&#44; S100 protein and vimentin &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Fig&#46; 1</a>&#41;&#44; indicative of LUL schwannoma&#46;</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia><p id="par0015" class="elsevierStylePara elsevierViewall">The LUL was lobectomized&#44; and the patient did not require any further treatment&#46;</p><p id="par0020" class="elsevierStylePara elsevierViewall">Schwannomas are extremely rare<a class="elsevierStyleCrossRef" href="#bib0030"><span class="elsevierStyleSup">1</span></a> benign tumors&#44; originating in the Schwann cells that produce the myelin sheath of the peripheral nerves&#46; The first case was described by Feckner in 1938&#44; and at least 80 cases have been published since then&#46; These are slow-growing tumors&#44; that do not infiltrate the neuronal axon&#44; but which can affect nerve conduction by extrinsic compression&#46; They appear in wide range of sites&#44; the most common of which are the skin and the tongue&#46;<a class="elsevierStyleCrossRef" href="#bib0035"><span class="elsevierStyleSup">2</span></a> Endobronchial presentation occurs in only 6&#37; of cases&#46;<a class="elsevierStyleCrossRefs" href="#bib0035"><span class="elsevierStyleSup">2&#44;3</span></a></p><p id="par0025" class="elsevierStylePara elsevierViewall">Schwannomas generally occur in middle age&#44; and no differences are observed between sexes&#46;<a class="elsevierStyleCrossRef" href="#bib0030"><span class="elsevierStyleSup">1</span></a> Clinical presentation can very&#44; and is determined by the size and location&#46; Early symptoms include asthma&#44; unproductive cough&#44; recurrent infections &#40;as in our case&#41;&#44; fever&#44; dyspnea and hemoptysis&#46;<a class="elsevierStyleCrossRefs" href="#bib0035"><span class="elsevierStyleSup">2&#44;3</span></a> Lesions tend to develop in the large bronchi or in bifurcatons&#46;<a class="elsevierStyleCrossRefs" href="#bib0040"><span class="elsevierStyleSup">3&#44;4</span></a> Up to 25&#37; may be multiple&#44; and they can even mimic metastasis&#44; if they occur concomitantly with other neoplasms&#46;<a class="elsevierStyleCrossRef" href="#bib0035"><span class="elsevierStyleSup">2</span></a> Radiographs can be useful in differential diagnosis&#44; but definitive diagnosis is usually obtained on fiberoptic bronchoscopy for atelectasis and secondary pneumonia&#44; as in our case&#46;<a class="elsevierStyleCrossRefs" href="#bib0035"><span class="elsevierStyleSup">2&#44;3</span></a></p><p id="par0030" class="elsevierStylePara elsevierViewall">On histological examination&#44; tumor cells are polygonal and fusiform&#44; with granular cytoplasma&#46; On IHC&#44; antigen expression is positive for S100 protein&#44; vimentin&#44; neuron-specific enolase&#44; and negative for keratins&#46;<a class="elsevierStyleCrossRef" href="#bib0045"><span class="elsevierStyleSup">4</span></a></p><p id="par0035" class="elsevierStylePara elsevierViewall">While endoscopic resection has been recommended for treating small lesions&#44; surgical resection is still the treatment of choice due to the risk of recurrence&#44; irrespective of tumor size&#46;<a class="elsevierStyleCrossRefs" href="#bib0040"><span class="elsevierStyleSup">3&#44;5</span></a> Prognosis is favorable&#44; and mean survival after surgery is longer than 5 years&#46;<a class="elsevierStyleCrossRef" href="#bib0030"><span class="elsevierStyleSup">1</span></a></p><span id="sec0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0005">Conflict of Interests</span><p id="par0040" class="elsevierStylePara elsevierViewall">The authors state that they have no conflict of interests&#46;</p></span></span>"
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        "nota" => "<p class="elsevierStyleNotepara" id="npar0005">Please cite this article as&#58; Landete P&#44; Chiner E&#44; Sancho-Chust JN&#44; P&#233;rez-Ferrer P&#46; Schwannoma bronquial&#44; un tumor poco frecuente&#46; Arch Bronconeumol&#46; 2015&#59;51&#58;471&#8211;472&#46;</p>"
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          "en" => "<p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">&#40;A&#41; An area of bronchial epithelium can be seen on lower magnification &#40;top right&#44; darker area&#41;&#46; The rest of the sample consists of tumor tissue&#46; &#40;B&#41; Fusiform cells and granular cytoplasma can been seen on greater magnification&#46; Bronchial schwannoma or granular cell tumor&#46; &#40;C&#41; Immunohistochemistry positive for S100 &#40;darker staining&#41;&#46;</p>"
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ISSN: 15792129
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