| Literature DB >> 19830524 |
Ryuhei Kitai1, Masato Sasaki, Kazufumi Sato, Toshihiko Kubota, Hiroaki Takeuchi, Yoshiaki Imamura.
Abstract
Mucosa-associated lymphoid tissue (MALT) lymphoma of the thymus is a rare condition, often characterized by its occurrence in a context of autoimmunity. We reported a first case of thymic MALT lymphoma following bilateral orbital pseudotumor. A 48-year-old man presented with bilateral exophthalmos diagnosed as orbital pseudotumor. His symptoms were relieved by an oral corticosteroid. Eleven years later, a mediastinal tumor was incidentally discovered. A thymectomy was performed, and histological examination revealed that the mass was a MALT lymphoma. There was no recurrence with no further treatment.Entities:
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Year: 2009 PMID: 19830524 DOI: 10.1007/s11748-009-0439-8
Source DB: PubMed Journal: Gen Thorac Cardiovasc Surg ISSN: 1863-6705