Ítem
Acceso Abierto

Hallazgos radiológicos de la enfermedad pulmonar en pacientes Colombianos con esclerodermia

dc.contributor.advisorAnaya, Juan-Manuel
dc.contributor.advisorMolano González,Nicolás
dc.creatorMorales, Adriana
dc.creatorPérez, Camila
dc.creatorMolano González, Nicolás
dc.creatorRojas-Villarraga, Adriana
dc.creatorCarrillo Bayona, Jorge Alberto
dc.creatorAnaya, Juan-Manuel
dc.creator.degreeEspecialista en Epidemiología (en Convenio con el CES)
dc.date.accessioned2015-11-13T20:50:29Z
dc.date.available2015-11-13T20:50:29Z
dc.date.created2015-06-26
dc.date.issued2015
dc.descriptionLa esclerosis sistémica (ES) es una enfermedad autoinmune multisistémica que afecta principalmente la piel, los pulmones, el tracto gastrointestinal, el corazón y los riñones. La enfermedad pulmonar, presente en casi el 100% de los casos, es el factor con mayor influencia en la mortalidad. El propósito de este estudio es realizar un análisis detallado de la enfermedad pulmonar por tomografía computarizada de alta resolución(TCAR) en pacientes Colombianos con ES, para lo cual se realizó un estudio de prevalencia analítica en 44 pacientes con ES valorados en el Hospital Universitario Mayor Méderi en los últimos 7 años. Los resultados mostraron características demográficas y clínicas similares a las previamente descritas. La prevalencia de enfermedad pulmonar intersticial fue alta, y los hallazgos de fibrosis pulmonar como vidrio esmerilado y panal de abejas se asociaron con la presencia del autoanticuerpo antiSCL70. La medida del diámetro esofágico por TCAR fue mayor en los pacientes con disfagia, antiSCL 70 y linfopenia, los cuales son marcadores de mal pronóstico.spa
dc.description.abstractSystemic sclerosis (SSc) is a multisystem autoimmune disease that primarily affects the skin, lungs, gastrointestinal tract, heart and kidneys. Lung disease, present in almost 100% of cases, is the most influential factor in mortality. The purpose of this study is to perform a detailed analysis of lung disease CT high resolution in Colombian patients with SSc, for which a study of analytical prevalence was performed in 44 patients with ES valued at University Hospital Mayor mederi in the last 7 years. The results showed demographic characteristics similar to those previously described clinics. The prevalence of interstitial lung disease was high, and the findings of pulmonary fibrosis as "ground glass" and "honeycomb" were associated with the presence of autoantibody antiSCL70. The measure HRCT esophageal diameter was greater in patients with dysphagia, antiSCL 70 and lymphopenia, which are markers of poor prognosis.eng
dc.format.mimetypeapplication/pdf
dc.identifier.doihttps://doi.org/10.48713/10336_11507
dc.identifier.urihttp://repository.urosario.edu.co/handle/10336/11507
dc.language.isospa
dc.publisherUniversidad del Rosariospa
dc.publisher.departmentFacultad de medicinaspa
dc.rights.accesRightsinfo:eu-repo/semantics/openAccess
dc.rights.accesoAbierto (Texto completo)spa
dc.rights.licenciaEL AUTOR, manifiesta que la obra objeto de la presente autorización es original y la realizó sin violar o usurpar derechos de autor de terceros, por lo tanto la obra es de exclusiva autoría y tiene la titularidad sobre la misma. PARGRAFO: En caso de presentarse cualquier reclamación o acción por parte de un tercero en cuanto a los derechos de autor sobre la obra en cuestión, EL AUTOR, asumirá toda la responsabilidad, y saldrá en defensa de los derechos aquí autorizados; para todos los efectos la universidad actúa como un tercero de buena fe. EL AUTOR, autoriza a LA UNIVERSIDAD DEL ROSARIO, para que en los términos establecidos en la Ley 23 de 1982, Ley 44 de 1993, Decisión andina 351 de 1993, Decreto 460 de 1995 y demás normas generales sobre la materia, utilice y use la obra objeto de la presente autorización. -------------------------------------- POLITICA DE TRATAMIENTO DE DATOS PERSONALES. Declaro que autorizo previa y de forma informada el tratamiento de mis datos personales por parte de LA UNIVERSIDAD DEL ROSARIO para fines académicos y en aplicación de convenios con terceros o servicios conexos con actividades propias de la academia, con estricto cumplimiento de los principios de ley. Para el correcto ejercicio de mi derecho de habeas data cuento con la cuenta de correo habeasdata@urosario.edu.co, donde previa identificación podré solicitar la consulta, corrección y supresión de mis datos.spa
dc.source.bibliographicCitationDenton CP, Black CM. Scleroderma--clinical and pathological advances. Best Pract Res Clin Rheumatol 2004;18:271–90.
dc.source.bibliographicCitationD’Angelo WA, Fries JF, Masi AT, Shulman LE. Pathologic observations in systemic sclerosis (scleroderma). A study of fifty-eight autopsy cases and fifty-eight matched controls. Am J Med 1969;46:428–40.
dc.source.bibliographicCitationBenan M, Hande I, Gul O. The natural course of progressive systemic sclerosis patients with interstitial lung involvement. Clin Rheumatol 2007;26:349–54.
dc.source.bibliographicCitationSolomon JJ, Olson AL, Fisher A, Bull T, Brown KK, Ganesh Raghu. Scleroderma lung disease. Eur Respir Updat 2013;22:6–19.
dc.source.bibliographicCitationBattle RW, Davitt MA, Cooper SM, Buckley LM, Leib ES, Beglin PA, et al. Prevalence of pulmonary hypertension in limited and diffuse scleroderma. Chest 1996;110:1515–9.
dc.source.bibliographicCitationMukerjee D, St George D, Coleiro B, Knight C, Denton CP, Davar J, et al. Prevalence and outcome in systemic sclerosis associated pulmonary arterial hypertension: application of a registry approach. Ann Rheum Dis 2003;62:1088–93.
dc.source.bibliographicCitationRojas-serrano J, Codina-velásquez H, Medrano-ramírez G, Simón JA. Menor incidencia de daño grave en órganos diana en pacientes mexicanos con esclerosis sistémica con afección cutánea difusa 2008;4:3–7.
dc.source.bibliographicCitationSampaio-Barros PD, Bortoluzzo AB, Marangoni RG, Rocha LF, Del Rio APT, Samara AM, et al. Survival, causes of death, and prognostic factors in systemic sclerosis: analysis of 947 Brazilian patients. J Rheumatol 2012;39:1971–8.
dc.source.bibliographicCitationLondoño J, Restrepo JF, Moreno R, Iglesias A, Rondon F, Peña M. Esclerodermia. Estudio descriptivo de 102 pacientes en el Hospital San Juan de Dios de Santa Fe de Bogotá. Rev Colomb Reumatol 1998;5:131–42.
dc.source.bibliographicCitationCoral-alvarado P, Rojas-villarraga A, Latorre MC, Mantilla RD, Restrepo JF, Pardo AL, et al. Risk Factors Associated with Pulmonary Arterial Hypertension in Colombian Patients with Systemic Sclerosis : Review of the Literature 2007:1–7.
dc.source.bibliographicCitationMedina YF, Ortiz M, Barrera N, Chalem P, Motta A, Zamora F, et al. Relación de los anticuerpos anti-péptido citrulinado con manifestaciones osteo-articulares en una cohorte de pacientes con esclerodermia of systemic sclerosis patients. Rev Colomb Reumatol 2011;18:155–62.
dc.source.bibliographicCitationRomero RM, Plata P, Castro L, Vélez P, Hernández N, Londoño J, et al. Correlación entre la clínica y los hallazgos histopatológicos en biopsia de piel en una cohorte de pacientes con esclerosis sistémica ( SS ) 2003.
dc.source.bibliographicCitationWalsh S, Fenster J. Geographical clustering of mortality from systemic sclerosis in the Southeastern United States, 1981-90. J Rheumatol 1997;24:2348–52.
dc.source.bibliographicCitationIoannidis J, Vlachoyiannopoulos P, Medsger T, Lucas M, Michet C, Kuwana M, et al. Mortality in systemic sclerosis: an international meta-analysis of individual patient data. Am J Med 2005;118:2–10.
dc.source.bibliographicCitationCoral-Alvarado P, Pardo AL, Castaño-Rodriguez N, Rojas-Villarraga A, Anaya J-M. Systemic sclerosis: a world wide global analysis. Clin Rheumatol 2009;28:757–65.
dc.source.bibliographicCitationBarnes J, Mayes MD. Epidemiology of systemic sclerosis : incidence , prevalence , survival , risk factors , malignancy , and environmental triggers 2012:165–70.
dc.source.bibliographicCitationIngegnoli F, Ardoino I, Boracchi P, Cutolo M, Airò P, Ananieva LP, et al. Nailfold capillaroscopy in systemic sclerosis : Data from the EULAR scleroderma trials and research ( EUSTAR ) database. Microvasc Res 2013;89:122–8.
dc.source.bibliographicCitationDiot E, Lesire V, Guilmot JL, Metzger MD, Pilore R, Rogier S, et al. Systemic sclerosis and occupational risk factors: a case-control study. Occup Environ Med 2002;59:545–9.
dc.source.bibliographicCitationKettaneh A, Al Moufti O, Tiev KP, Chayet C, Tolédano C, Fabre B, et al. Occupational exposure to solvents and gender-related risk of systemic sclerosis: a metaanalysis of case-control studies. J Rheumatol 2007;34:97–103.
dc.source.bibliographicCitationVan den Hoogen F, Khanna D, Fransen J, Johnson SR, Baron M, Tyndall A, et al. 2013 classification criteria for systemic sclerosis: an American College of Rheumatology/European League against Rheumatism collaborative initiative. Arthritis Rheum 2013;65:2737–47.
dc.source.bibliographicCitationNihtyanova SI, Schreiber BE, Ong VH, Rosenberg D, Moinzadeh P, Coghlan JG, et al. Prediction of pulmonary complications and long-term survival in systemic sclerosis. Arthritis Rheum 2014;66:1625–35.
dc.source.bibliographicCitationHant FN, Herpel LB, Silver RM. Pulmonary Manifestations of Scleroderma and Mixed Connective Tissue Disease. Clin Chest Med 2010;31:433–49.
dc.source.bibliographicCitationMcNearney TA, Reveille JD, Fischbach M, Friedman AW, Lisse JR, Goel N, et al. Pulmonary involvement in systemic sclerosis: Associations with genetic, serologic, sociodemographic, and behavioral factors. Arthritis Care Res 2007;57:318–26.
dc.source.bibliographicCitationGreidinger EL, Flaherty KT, White B, Rosen A, Wigley FM, Wise RA. African-American race and antibodies to topoisomerase I are associated with increased severity of scleroderma lung disease. Chest 1998;114:801–7.
dc.source.bibliographicCitationSteele R, Hudson M, Lo E, Baron M. Clinical decision rule to predict the presence of interstitial lung disease in systemic sclerosis. Arthritis Care Res (Hoboken) 2012;64:519–24.
dc.source.bibliographicCitationLewandowska K, Ciurzynski M, Gorska E, Bienias P, Irzyk K, Siwicka M, et al. Antiendothelial cells antibodies in patients with systemic sclerosis in relation to pulmonary hypertension and lung fibrosis. Adv. Exp. Med. Biol., vol. 756, 2013, p. 147–53.
dc.source.bibliographicCitationCoral-Alvarado P, Rojas-Villarraga A, Latorre MC, Mantilla RD, Restrepo JF, Pardo AL, et al. Risk factors associated with pulmonary arterial hypertension in Colombian patients with systemic sclerosis: review of the literature. J Rheumatol 2008;35:244–50.
dc.source.bibliographicCitationMayes MD, Lacey J V., Beebe-Dimmer J, Gillespie BW, Cooper B, Laing TJ, et al. Prevalence, incidence, survival, and disease characteristics of systemic sclerosis in a large US population. Arthritis Rheum 2003;48:2246–55.
dc.source.bibliographicCitationFautrel B, Sordet C, Chatelus E, Sibilia J. Incidence and Prevalence of Systemic Sclerosis : A Systematic 2008:223–35.
dc.source.bibliographicCitationRosa JE, Soriano ER, Narvaez-Ponce L, del Cid CC, Imamura PM, Catoggio LJ. Incidence and prevalence of systemic sclerosis in a healthcare plan in Buenos Aires. J Clin Rheumatol 2011;17:59–63.
dc.source.bibliographicCitationArias-Nuñez MC, Llorca J, Vazquez-Rodriguez TR, Gomez-Acebo I, Miranda-Filloy JA, Martin J, et al. Systemic sclerosis in northwestern Spain: a 19-year epidemiologic study. Medicine (Baltimore) 2008;87:272–80.
dc.source.bibliographicCitationTamby MC, Chanseaud Y, Guillevin L, Mouthon L. New insights into the pathogenesis of systemic sclerosis. Autoimmun Rev 2003;2:152–7.
dc.source.bibliographicCitationLaing TJ, Gillespie BW, Toth MB, Mayes MD, Gallavan RH, Burns CJ, et al. Racial differences in scleroderma among women in Michigan. Arthritis Rheum 1997;40:734–42.
dc.source.bibliographicCitationWeaver A, Divertie M, Titus J. Pulmonary scleroderma. Dis Chest 1968;176:755–9.
dc.source.bibliographicCitationSchurawitzki H, Stiglbauer R, Graninger W, Herold C, Pölzleitner D, Burghuber OC, et al. Interstitial lung disease in progressive systemic sclerosis: high-resolution CT versus radiography. Radiology 1990;176:755–9.
dc.source.bibliographicCitationGu YS, Kong J, Cheema GS, Keen CL, Wick G, Gershwin ME. The immunobiology of systemic sclerosis. Semin Arthritis Rheum 2008;38:132–60.
dc.source.bibliographicCitationBussone G, Mouthon L. Interstitial lung disease in systemic sclerosis. Autoimmun Rev 2011;10:248–55.
dc.source.bibliographicCitationSfikakis PP. Is IL-4 a potential therapeutic target in systemic sclerosis-associated pulmonary fibrosis? Clin Immunol 2011;141:240–1.
dc.source.bibliographicCitationVeraldi KL, Hsu E, Feghali-Bostwick C a. Pathogenesis of pulmonary fibrosis in systemic sclerosis: lessons from interstitial lung disease. Curr Rheumatol Rep 2010;12:19–25.
dc.source.bibliographicCitationBogatkevich GS, Ludwicka-Bradley A, Highland KB, Hant F, Nietert PJ, Singleton CB, et al. Impairment of the antifibrotic effect of hepatocyte growth factor in lung fibroblasts from African Americans: Possible role in systemic sclerosis. Arthritis Rheum 2007;56:2432–42.
dc.source.bibliographicCitationDemir N, Sahin A, Küçükşahin O, Kayacan O, Dinçer I, Sayın T, et al. Pulmonary arterial hypertension and systemic sclerosis relation: a single centre experience. Heart Lung Circ 2014;23:667–73.
dc.source.bibliographicCitationTheodore AC, Tseng C-H, Li N, Elashoff RM, Tashkin DP. Correlation of cough with disease activity and treatment with cyclophosphamide in scleroderma interstitial lung disease: findings from the Scleroderma Lung Study. Chest 2012;142:614–21.
dc.source.bibliographicCitationSchettino I a L, Ab’Saber AM, Vollmer R, Saldiva PHN, Carvalho CRR, Kairalla R a, et al. Accuracy of high resolution CT in assessing idiopathic pulmonary fibrosis histology by objective morphometric index. Pathol Res Pract 2002;198:347–54.
dc.source.bibliographicCitationLaunay D, Remy-Jardin M, Michon-Pasturel U, Mastora I, Hachulla E, Lambert M, et al. High resolution computed tomography in fibrosing alveolitis associated with systemic sclerosis. J Rheumatol 2006;33:1789–801.
dc.source.bibliographicCitationPernot J, Puzenat E, Magy-Bertrand N, Manzoni P, Gondouin A, Bourdin H, et al. Detection of interstitial lung disease in systemic sclerosis through partitioning of lung transfer for carbon monoxide. Respiration 2012;84:461–8.
dc.source.bibliographicCitationQuadrelli S a, Molinari L, Ciallella LM, Bosio M, Salvado A. Patterns of pulmonary function in smoking and nonsmoking patients with progressive systemic sclerosis. Rheumatol Int 2009;29:995–9.
dc.source.bibliographicCitationGoh NSL, Desai SR, Veeraraghavan S, Hansell DM, Copley SJ, Maher TM, et al. Interstitial lung disease in systemic sclerosis: a simple staging system. Am J Respir Crit Care Med 2008;177:1248–54.
dc.source.bibliographicCitationSteen VD, Conte C, Owens GR, Medsger TA. Severe restrictive lung disease in systemic sclerosis. Arthritis Rheum 1994;37:1283–9.
dc.source.bibliographicCitationKhanna D, Tseng C-H, Farmani N, Steen V, Furst DE, Clements PJ, et al. Clinical course of lung physiology in patients with scleroderma and interstitial lung disease: analysis of the Scleroderma Lung Study Placebo Group. Arthritis Rheum 2011;63:3078–85.
dc.source.bibliographicCitationGarin MC, Highland KB, Silver RM, Strange C. Limitations to the 6-minute walk test in interstitial lung disease and pulmonary hypertension in scleroderma. J Rheumatol 2009;36:330–6.
dc.source.bibliographicCitationPatiwetwitoon S, Wangkaew S, Euathrongchit J, Kasitanon N, Louthrenoo W. High-resolution computed tomographic findings in systemic sclerosis-associated interstitial lung disease: comparison between diffuse and limited systemic sclerosis. J Clin Rheumatol 2012;18:229–33.
dc.source.bibliographicCitationBouros D, Wells AU, Nicholson AG, Colby T V, Polychronopoulos V, Pantelidis P, et al. Histopathologic subsets of fibrosing alveolitis in patients with systemic sclerosis and their relationship to outcome. Am J Respir Crit Care Med 2002;165:1581–6.
dc.source.bibliographicCitationTravis WD, Costabel U, Hansell DM, King TE, Jr., Lynch DA, et al. An official AmericanThoracic Society / European Respiratory Society Statement: Update od the International Multidisciplinary Classification of the Idiopathic Interstitial Pneumonias. Am J Respir Crit Care Med 2013;188:733–48.
dc.source.bibliographicCitationCottin V, Donsbeck A V, Revel D, Loire R, Cordier JF. Nonspecific interstitial pneumonia. Individualization of a clinicopathologic entity in a series of 12 patients. Am J Respir Crit Care Med 1998;158:1286–93.
dc.source.bibliographicCitationKim TS, Lee KS, Chung MP, Han J, Park JS, Hwang JH, et al. Nonspecific interstitial pneumonia with fibrosis: high-resolution CT and pathologic findings. AJR Am J Roentgenol 1998;171:1645–50.
dc.source.bibliographicCitationPark CS, Jeon JW, Park SW, Lim GI, Jeong SH, Uh ST, et al. Nonspecific interstitial pneumonia/fibrosis: clinical manifestations, histologic and radiologic features. Korean J Intern Med 1996;11:122–32.
dc.source.bibliographicCitationBellia M, Cannizzaro F, Scichilone N, Riili M, Triolo G, Midiri M, et al. HRCT and scleroderma: semiquantitative evaluation of lung damage and functional abnormalities. Radiol Med 2009;114:190–203.
dc.source.bibliographicCitationParra ER, Otani LH, Carvalho EF De, Saber AA, Capelozzi VL. Systemic sclerosis and idiophatic interstitial pneumonia: histomorphometric differences in lung biopsies 2009;35:529–40.
dc.source.bibliographicCitationDe Carvalho EF, Parra ER, De Souza R, A’B Saber AM, De Carvalho Machado J, Capelozzi VL. Arterial and interstitial remodelling processes in non-specific interstitial pneumonia: Systemic sclerosis versus idiopathic. Histopathology 2008;53:195–204.
dc.source.bibliographicCitationTaylor JG, Bolster MB. Bronchiolitis obliterans with organizing pneumonia associated with scleroderma and scleroderma spectrum diseases. J Clin Rheumatol 2003;9:239–45.
dc.source.bibliographicCitationShimizu Y, Tsukagoshi H, Nemoto T, Honma M, Nojima Y, Mori M. Recurrent bronchiolitis obliterans organizing pneumonia in a patient with limited cutaneous systemic sclerosis. Rheumatol Int 2002;22:216–8.
dc.source.bibliographicCitationBridges AJ, Hsu KC, Dias-Arias AA, Chechani V. Bronchiolitis obliterans organizing pneumonia and scleroderma. J Rheumatol 1992;19:1136–40.
dc.source.bibliographicCitationMuir TE, Tazelaar HD, Colby T V, Myers JL. Organizing diffuse alveolar damage associated with progressive systemic sclerosis. Mayo Clin Proc 1997;72:639–42.
dc.source.bibliographicCitationGluecker T, Capasso P, Schnyder P, Gudinchet F, Schaller M-D, Revelly J-P. Clinical and Radiologic Features of Pulmonary Edema. Radiographics 1999;19:1507–31.
dc.source.bibliographicCitationCottin V, Nunes H, Mouthon L, Gamondes D, Lazor R, Hachulla E, et al. Combined pulmonary fibrosis and emphysema syndrome in connective tissue disease. Arthritis Rheum 2011;63:295–304.
dc.source.bibliographicCitationDesai SR, Veeraraghavan S, Hansell DM, Nikolakopolou A, Goh NSL, Nicholson AG, et al. CT features of lung disease in patients with systemic sclerosis: comparison with idiopathic pulmonary fibrosis and nonspecific interstitial pneumonia. Radiology 2004;232:560–7.
dc.source.bibliographicCitationRoman MJ, Salmon JE. Cardiovascular manifestations of rheumatologic diseases. Circulation 2007;116:2346–55.
dc.source.bibliographicCitationBauer PR, Schiavo DN, Osborn TG, Levin DL, St Sauver J, Hanson AC, et al. Influence of interstitial lung disease on outcome in systemic sclerosis: a population-based historical cohort study. Chest 2013;144:571–7.
dc.source.bibliographicCitationZompatori M, Leone MB, Giannotta M, Galie N, Palazzini M, Reggiani ML, et al. Pulmonary hypertension and systemic sclerosis: the role of high-resolution computed tomography. Radiol Med 2013;118:1360–72.
dc.source.bibliographicCitationMcCall RK, Ravenel JG, Nietert PJ, Granath A, Silver RM. Relationship of main pulmonary artery diameter to pulmonary arterial pressure in scleroderma patients with and without interstitial fibrosis. J Comput Assist Tomogr 2014;38:163–8.
dc.source.bibliographicCitationGünther S, Jaïs X, Maitre S, Bérezné a, Dorfmüller P, Seferian a, et al. Computed tomography findings of pulmonary venoocclusive disease in scleroderma patients presenting with precapillary pulmonary hypertension. Arthritis Rheum 2012;64:2995–3005.
dc.source.bibliographicCitationMcGuire F, Kennelly T, Tillack T, Robbins M. Pulmonary capillary hemangiomatosis associated with CREST syndrome: a case report and review of the literature. Respiration 2010;80:435–8.
dc.source.bibliographicCitationNakanishi N. 2009 ESC/ERS Pulmonary Hypertension Guidelines and Connective Tissue Disease. Allergol Int 2011;60:419–24.
dc.source.bibliographicCitationGugnani MK, Pierson C, Vanderheide R, Girgis RE. Pulmonary edema complicating prostacyclin therapy in pulmonary hypertension associated with scleroderma: A case of pulmonary capillary hemangiomatosis. Arthritis Rheum 2000;43:699–703.
dc.source.bibliographicCitationJohnson SR, Patsios D, Hwang DM, Granton JT. Pulmonary veno-occlusive disease and scleroderma associated pulmonary hypertension. J Rheumatol 2006;33:2347–50.
dc.source.bibliographicCitationChaer R a, Massad MG, Evans a, Olopade C, Varga J. Systemic sclerosis complicated by diffuse alveolar hemorrhage. Med Sci Monit 2001;7:1013–5.
dc.source.bibliographicCitationPrather AD, Smith TR, Poletto DM, Tavora F, Chung JH, Nallamshetty L, et al. Aspiration-related lung diseases. J Thorac Imaging 2014;29:304–9.
dc.source.bibliographicCitationLichtenstein J, Aispaugh P, Blebea J, Donnelly L, Gasparaitis A, Blaise J, et al. Image interpretation Session: 1995. Radiographics 1996;16:215–39.
dc.source.bibliographicCitationYousem SA, Dacic S. Idiopathic bronchiolocentric interstitial pneumonia. Mod Pathol 2002;15:1148–53.
dc.source.bibliographicCitationDe Carvalho M-EP, Kairalla RA, Capelozzi VL, Deheinzelin D, do Nascimento Saldiva PH, de Carvalho CRR. Centrilobular fibrosis: a novel histological pattern of idiopathic interstitial pneumonia. Pathol Res Pract 2002;198:577–83.
dc.source.bibliographicCitationCordier J-F. Challenges in pulmonary fibrosis. 2: Bronchiolocentric fibrosis. Thorax 2007;62:638–49.
dc.source.bibliographicCitationDe Souza RBC, Borges CTL, Capelozzi VL, Parra ER, Jatene FB, Kavakama J, et al. Centrilobular fibrosis: An underrecognized pattern in systemic sclerosis. Respiration 2009;77:389–97.
dc.source.bibliographicCitationMorgan C, Knight C, Lunt M, Black CM, Silman AJ. Predictors of end stage lung disease in a cohort of patients with scleroderma. Ann Rheum Dis 2003;62:146–50.
dc.source.bibliographicCitationMeier FMP, Frommer KW, Dinser R, Walker U a, Czirjak L, Denton CP, et al. Update on the profile of the EUSTAR cohort: an analysis of the EULAR Scleroderma Trials and Research group database. Ann Rheum Dis 2012;71:1355–60.
dc.source.bibliographicCitationManno R, Wigley FM, Gelber AC. LATE-AGE ONSET SCLERODERMA. J Rheumatol 2012;38:1317–25.
dc.source.bibliographicCitationAl-dhaher FF, Pope JE. Determinants of Morbidity and Mortality of Systemic Sclerosis in Canada. YSARH 2010;39:269–77.
dc.source.bibliographicCitationMerkel P a, Silliman NP, Clements PJ, Denton CP, Furst DE, Mayes MD, et al. Patterns and predictors of change in outcome measures in clinical trials in scleroderma: an individual patient meta-analysis of 629 subjects with diffuse cutaneous systemic sclerosis. Arthritis Rheum 2012;64:3420–9.
dc.source.bibliographicCitationSampaio-Barros PD, Bortoluzzo AB, Marangoni RG, Rocha LF, Del Rio APT, Samara AM, et al. Survival, causes of death, and prognostic factors in systemic sclerosis: analysis of 947 Brazilian patients. J Rheumatol 2012;39:1971–8.
dc.source.bibliographicCitationPoormoghim H, Lucas M, Fertig N, Medsger TA. SYSTEMIC SCLEROSIS SINE SCLERODERMA Demographic , Clinical , and Serologic Features and Survival in Forty-Eight Patients. Arthritis Rheum 2000;43:444–51.
dc.source.bibliographicCitationHashimoto A, Endo H, Kondo H, Hirohata S. Clinical features of 405 Japanese patients with systemic sclerosis. Mod Rheumatol 2012;22:272–9.
dc.source.bibliographicCitationPandey AK, Wilcox P, Mayo JR, Moss R, Ellis J, Brown J, et al. Oesophageal dilatation on high-resolution CT chest in systemic sclerosis: what does it signify? J Med Imaging Radiat Oncol 2011;55:551–5.
dc.source.bibliographicCitationBhalla M, Silver R, Shepard J-A, McLoud T. Chest CT in Patients with Scieroderma : Prevalence of Asymptomatic Esophageal Mediastinal Lymphadenopathy. AJR Am J Roentgenol 1993;161:269–72.
dc.source.bibliographicCitationPandey AK, Wilcox P, Mayo JR, Moss R, Ellis J, Brown J, et al. Oesophageal dilatation on high-resolution CT chest in systemic sclerosis: what does it signify? J Med Imaging Radiat Oncol 2011;55:551–5.
dc.source.bibliographicCitationKinuya K, Nakajima K, Kinuya S. Esophageal hypomotility in systemic sclerosis : Close relationship with pulmonary involvement 2001;15:97–101.
dc.source.bibliographicCitationMarie I, Dominique S, Levesque H, Ducrotté P, Denis P, Hellot MF, et al. Esophageal involvement and pulmonary manifestations in systemic sclerosis. Arthritis Rheum 2001;45:346–54.
dc.source.bibliographicCitationEbert EC. Esophageal disease in scleroderma. J Clin Gastroenterol 2006;40:769–75.
dc.source.bibliographicCitationLambova S, Müller-Ladner U. Pulmonary arterial hypertension in systemic sclerosis. Autoimmun Rev 2010;9:761–70.
dc.source.bibliographicCitationChampion HC. The Heart in Scleroderma. Rheum Dis Clin North Am 2009;34:1–8.
dc.source.bibliographicCitationHachulla a-L, Launay D, Gaxotte V, de Groote P, Lamblin N, Devos P, et al. Cardiac magnetic resonance imaging in systemic sclerosis: a cross-sectional observational study of 52 patients. Ann Rheum Dis 2009;68:1878–84.
dc.source.bibliographicCitationDesai C, Lee D, Sanjiv S. Systemic sclerosis and the heart: current diagnosis and management. Curr Opin Rheumatol 2013;23:545–54.
dc.source.bibliographicCitationUresandi F, Monreal M, García-bragado F, Domenech P, Lecumberri R, Escribano P, et al. Consenso nacional sobre el diagnóstico , estratificación de riesgo y tratamiento de los pacientes con tromboembolia pulmonar. National Consensus on the Diagnosis , Risk Stratification and Treatment of Patients with Pulmonary Embolism. Arch Bronconeumol 2014;49:534–47.
dc.source.bibliographicCitationChung W-S, Lin C-L, Sung F-C, Hsu W-H, Yang W-T, Lu C-C, et al. Systemic sclerosis increases the risks of deep vein thrombosis and pulmonary thromboembolism: a nationwide cohort study. Rheumatology (Oxford) 2014;53:1639–45.
dc.source.instnameinstname:Universidad del Rosariospa
dc.source.reponamereponame:Repositorio Institucional EdocURspa
dc.subjectEsclerodermiaspa
dc.subjectenfermedad pulmonarspa
dc.subjectfibrosis pulmonarspa
dc.subjecthipertensión pulmonarspa
dc.subjectesofagopatíaspa
dc.subject.ddcEnfermedades
dc.subject.decsEnfermedades Pulmonaresspa
dc.subject.decsFibrosis Pulmonarspa
dc.subject.decsEsclerodermia Sistémicaspa
dc.subject.keywordSystemic sclerosiseng
dc.subject.keywordpulmonary diseaseeng
dc.subject.keywordpulmonary fibrosiseng
dc.subject.keywordpulmonary hypertensioneng
dc.subject.keywordesophagopathyeng
dc.subject.lembEpidemiologíaspa
dc.subject.lembEnfermedades de los pulmonesspa
dc.titleHallazgos radiológicos de la enfermedad pulmonar en pacientes Colombianos con esclerodermiaspa
dc.title.TranslatedTitleRadiologic findings of pulmonary involvement in Colombian patients with systemic sclerosiseng
dc.typebachelorThesiseng
dc.type.hasVersioninfo:eu-repo/semantics/acceptedVersion
dc.type.spaTrabajo de gradospa
Archivos
Bloque original
Mostrando1 - 1 de 1
Cargando...
Miniatura
Nombre:
TesisFinal.pdf
Tamaño:
3.83 MB
Formato:
Adobe Portable Document Format
Descripción:
Artículo principal