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    "textoCompleto" => "<span class="elsevierStyleSections"><p id="par0005" class="elsevierStylePara elsevierViewall">A 30-year-old man with no significant history presented in the emergency department in 2007 with loss of vision&#46; A campimetric defect indicative of optic neuritis was confirmed&#46; In view of these findings&#44; corticosteroid treatment &#40;1<span class="elsevierStyleHsp" style=""></span>g&#47;day for 5 days&#41; was administered&#44; and magnetic resonance imaging &#40;MRI&#41; of the head was performed&#46; No radiological studies of the chest were performed during this episode&#46; The head MRI &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Fig&#46; 1</a>&#41; showed focal lesions in the white matter&#44; indicative of demyelinating disease&#46; Since the patient did not meet all the criteria for multiple sclerosis &#40;MS&#41; and had presented no new episodes of neurological symptoms during follow-up&#44; no specific MS treatment was initiated and the patient continued follow-up on an outpatient basis&#46;</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia><p id="par0010" class="elsevierStylePara elsevierViewall">Several follow-up head MRIs were performed&#44; showing mild disease progression with no clinical repercussions&#44; and the presumed diagnosis of MS was maintained&#46; Six years after this episode&#44; the patient presented with cough and dyspnea&#46; A chest X-ray &#40;<a class="elsevierStyleCrossRef" href="#fig0010">Fig&#46; 2</a>A&#41; showed widened mediastinum&#44; enlarged pulmonary hila&#44; and interstitial involvement&#46; In view of the radiological suspicion of sarcoidosis&#44; a chest CT was performed&#46; Multiple lymphadenopathies in the mediastinum and both pulmonary hila and severe interstitial involvement were confirmed on CT &#40;<a class="elsevierStyleCrossRef" href="#fig0010">Fig&#46; 2</a>B&#41;&#46; Presumed radiological diagnosis was sarcoidosis &#40;stage II&#41;&#44; confirmed on histology of a transbronchial biopsy specimen&#46; After treatment began with systemic and inhaled corticosteroids&#44; the patient&#39;s clinical and radiological picture improved &#40;<a class="elsevierStyleCrossRef" href="#fig0010">Fig&#46; 2</a>D&#41;&#46; A repeat CT of the head showed stabilization of the lesions with respect to the previous examination&#46;</p><elsevierMultimedia ident="fig0010"></elsevierMultimedia><p id="par0020" class="elsevierStylePara elsevierViewall">Sarcoidosis is a multisystemic disease of unknown origin that typically affects the lung and intrathoracic lymph nodes&#44; although it can affect the eye&#44; liver&#44; heart&#44; spleen&#44; saliva glands&#44; bone and central nervous system&#46;<a class="elsevierStyleCrossRefs" href="#bib0030"><span class="elsevierStyleSup">1&#44;2</span></a> Neurosarcoidosis is uncommon &#40;5&#37; of all patients&#41; and is usually diagnosed by a process of elimination&#44; given the difficulty of obtaining biological samples&#46;<a class="elsevierStyleCrossRef" href="#bib0040"><span class="elsevierStyleSup">3</span></a> Nevertheless&#44; awareness of this entity may facilitate prompt diagnosis and prevent the development of neurological deficits&#46; Moreover&#44; mistreatment of neurosarcoidosis with interferon &#40;as used in some MS patients&#41; may lead to worsening of the disease&#46;<a class="elsevierStyleCrossRefs" href="#bib0045"><span class="elsevierStyleSup">4&#44;5</span></a> The unusual feature of our case is that the patient had been initially diagnosed with probable MS&#44; but 6 years later&#44; in the light of radiological findings in the chest&#44; sarcoidosis was suggested&#46; In view of the lack of clinical activity of the presumed demyelinating disease&#44; clinicians from the Pulmonology&#44; Neurology and Radiology departments agreed to change the initial clinical suspicion of MS to sarcoidosis with neurological involvement&#46; This case demonstrates the complexity of diagnosing this disease in patients whose initial clinical symptoms are neurological&#44; and the importance of including sarcoidosis in the differential diagnosis of demyelinating diseases of the central nervous system&#46;</p></span>"
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Letter to the Editor
Sarcoidosis With Neurological Involvement Imitating Multiple Sclerosis: The Importance of Thoracic Imaging
Sarcoidosis con afectación neurológica simulando una esclerosis múltiple: importancia de la imagen torácica
Carmen Picón Serrano
Corresponding author
cpiconserrano@gmail.com

Corresponding author.
, Sara Escoda Menéndez, Luis Gorospe Sarasúa
Departamento de Radiodiagnóstico, Hospital Universitario Ramón y Cajal, Madrid, Spain
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          "en" => "<p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">Magnetic resonance imaging &#40;MRI&#41; of the head in T2 &#40;A&#41; showing a hyperintense focal lesion in the splenium of the corpus callosum &#40;white arrow&#41;&#46; Axial FLAIR image &#40;B&#41; showing a hyperintense focal lesion in the periventricular white matter &#40;white arrow&#41;&#46; Both lesions are radiologically non-specific&#44; but in the right clinical context can be indicative of demyelinating disease&#46;</p>"
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    "textoCompleto" => "<span class="elsevierStyleSections"><p id="par0005" class="elsevierStylePara elsevierViewall">A 30-year-old man with no significant history presented in the emergency department in 2007 with loss of vision&#46; A campimetric defect indicative of optic neuritis was confirmed&#46; In view of these findings&#44; corticosteroid treatment &#40;1<span class="elsevierStyleHsp" style=""></span>g&#47;day for 5 days&#41; was administered&#44; and magnetic resonance imaging &#40;MRI&#41; of the head was performed&#46; No radiological studies of the chest were performed during this episode&#46; The head MRI &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Fig&#46; 1</a>&#41; showed focal lesions in the white matter&#44; indicative of demyelinating disease&#46; Since the patient did not meet all the criteria for multiple sclerosis &#40;MS&#41; and had presented no new episodes of neurological symptoms during follow-up&#44; no specific MS treatment was initiated and the patient continued follow-up on an outpatient basis&#46;</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia><p id="par0010" class="elsevierStylePara elsevierViewall">Several follow-up head MRIs were performed&#44; showing mild disease progression with no clinical repercussions&#44; and the presumed diagnosis of MS was maintained&#46; Six years after this episode&#44; the patient presented with cough and dyspnea&#46; A chest X-ray &#40;<a class="elsevierStyleCrossRef" href="#fig0010">Fig&#46; 2</a>A&#41; showed widened mediastinum&#44; enlarged pulmonary hila&#44; and interstitial involvement&#46; In view of the radiological suspicion of sarcoidosis&#44; a chest CT was performed&#46; Multiple lymphadenopathies in the mediastinum and both pulmonary hila and severe interstitial involvement were confirmed on CT &#40;<a class="elsevierStyleCrossRef" href="#fig0010">Fig&#46; 2</a>B&#41;&#46; Presumed radiological diagnosis was sarcoidosis &#40;stage II&#41;&#44; confirmed on histology of a transbronchial biopsy specimen&#46; After treatment began with systemic and inhaled corticosteroids&#44; the patient&#39;s clinical and radiological picture improved &#40;<a class="elsevierStyleCrossRef" href="#fig0010">Fig&#46; 2</a>D&#41;&#46; A repeat CT of the head showed stabilization of the lesions with respect to the previous examination&#46;</p><elsevierMultimedia ident="fig0010"></elsevierMultimedia><p id="par0020" class="elsevierStylePara elsevierViewall">Sarcoidosis is a multisystemic disease of unknown origin that typically affects the lung and intrathoracic lymph nodes&#44; although it can affect the eye&#44; liver&#44; heart&#44; spleen&#44; saliva glands&#44; bone and central nervous system&#46;<a class="elsevierStyleCrossRefs" href="#bib0030"><span class="elsevierStyleSup">1&#44;2</span></a> Neurosarcoidosis is uncommon &#40;5&#37; of all patients&#41; and is usually diagnosed by a process of elimination&#44; given the difficulty of obtaining biological samples&#46;<a class="elsevierStyleCrossRef" href="#bib0040"><span class="elsevierStyleSup">3</span></a> Nevertheless&#44; awareness of this entity may facilitate prompt diagnosis and prevent the development of neurological deficits&#46; Moreover&#44; mistreatment of neurosarcoidosis with interferon &#40;as used in some MS patients&#41; may lead to worsening of the disease&#46;<a class="elsevierStyleCrossRefs" href="#bib0045"><span class="elsevierStyleSup">4&#44;5</span></a> The unusual feature of our case is that the patient had been initially diagnosed with probable MS&#44; but 6 years later&#44; in the light of radiological findings in the chest&#44; sarcoidosis was suggested&#46; In view of the lack of clinical activity of the presumed demyelinating disease&#44; clinicians from the Pulmonology&#44; Neurology and Radiology departments agreed to change the initial clinical suspicion of MS to sarcoidosis with neurological involvement&#46; This case demonstrates the complexity of diagnosing this disease in patients whose initial clinical symptoms are neurological&#44; and the importance of including sarcoidosis in the differential diagnosis of demyelinating diseases of the central nervous system&#46;</p></span>"
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        "nota" => "<p class="elsevierStyleNotepara" id="npar0005">Please cite this article as&#58; Pic&#243;n Serrano C&#44; Escoda Men&#233;ndez S&#44; Gorospe Saras&#250;a L&#46; Sarcoidosis con afectaci&#243;n neurol&#243;gica simulando una esclerosis m&#250;ltiple&#58; importancia de la imagen tor&#225;cica&#46; Arch Bronconeumol&#46; 2015&#59;51&#58;307-308&#46;</p>"
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          "en" => "<p id="spar0010" class="elsevierStyleSimplePara elsevierViewall">Chest X-ray &#40;A&#41; showing a widened mediastinum&#44; enlarged pulmonary hila and interstitial involvement&#46; Chest computed tomography confirming presence of large mediastinal lymphadenopathies&#44; and bilateral hilar &#40;B&#44; coronal reconstruction with intravenous contrast medium&#41; and pulmonary parenchymal &#40;C&#44; axial image in lung window&#41; involvement&#46; Chest X-ray &#40;D&#41; obtained 6 months after starting corticosteroid treatment showing normalization of findings&#46;</p>"
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Article information
ISSN: 15792129
Original language: English
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