Myasthenia gravis and thymoma coexisting with myotonic dystrophy type 1

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dc.contributor.authorEkmekci, Ozgul
dc.contributor.authorKarasoy, Hatice
dc.contributor.authorBademkiran, Fikret
dc.contributor.authorAkkus, Dilek Evyapan
dc.contributor.authorYuceyar, Nur
dc.date.accessioned2019-10-27T22:06:04Z
dc.date.available2019-10-27T22:06:04Z
dc.date.issued2014
dc.departmentEge Üniversitesien_US
dc.description.abstractWe describe a 34-year old man presenting with subacute generalized myasthenic symptoms. His clinical features and laboratory investigations demonstrated both myasthenia gravis and myotonic dystrophy type 1. The computerized tomography of chest revealed anterior mediastinal mass. The lymphocyte-rich thymoma was removed surgically and he received radiotherapy. Recent observations suggested that the patients with myotonic dystrophy may have an increased risk of benign and malignant tumours but its coexistence with thymoma is very rare. The risk of thymoma associated with myotonic dystrophy is unknown. (C) 2013 The Authors. Published by Elsevier B.V. All rights reserved.en_US
dc.identifier.doi10.1016/j.nmd.2013.09.001en_US
dc.identifier.endpage42en_US
dc.identifier.issn0960-8966
dc.identifier.issn1873-2364
dc.identifier.issue1en_US
dc.identifier.pmid24291332en_US
dc.identifier.scopusqualityQ1en_US
dc.identifier.startpage40en_US
dc.identifier.urihttps://doi.org/10.1016/j.nmd.2013.09.001
dc.identifier.urihttps://hdl.handle.net/11454/48698
dc.identifier.volume24en_US
dc.identifier.wosWOS:000331415100007en_US
dc.identifier.wosqualityQ2en_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.indekslendigikaynakScopusen_US
dc.indekslendigikaynakPubMeden_US
dc.language.isoenen_US
dc.publisherPergamon-Elsevier Science Ltden_US
dc.relation.ispartofNeuromuscular Disordersen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectMyotonic dystrophyen_US
dc.subjectThymomaen_US
dc.subjectNeoplasmen_US
dc.titleMyasthenia gravis and thymoma coexisting with myotonic dystrophy type 1en_US
dc.typeArticleen_US

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