| Literature DB >> 24291332 |
Ozgul Ekmekci1, Hatice Karasoy2, Fikret Bademkiran2, Dilek Evyapan Akkus2, Nur Yuceyar2.
Abstract
We 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.Entities:
Keywords: Myotonic dystrophy; Neoplasm; Thymoma
Mesh:
Year: 2013 PMID: 24291332 DOI: 10.1016/j.nmd.2013.09.001
Source DB: PubMed Journal: Neuromuscul Disord ISSN: 0960-8966 Impact factor: 4.296