| Literature DB >> 15754301 |
Fumiyuki Takahashi1, Koji Tsuta, Yoshihiro Matsuno, Kazuhisa Takahashi, Michie Toba, Koichi Sato, Toshimasa Uekusa, Hiroshi Izumi, Kazuhiro Nakamura, Sachiko Hirose, Yoshinosuke Fukuchi.
Abstract
Primary thymic adenocarcinoma, mucinous subtype, is extremely rare with only one case reported to date. We describe herein a case of thymic mucinous adenocarcinoma. A 59-year-old man was identified to have an anterior mediastinal tumor and was diagnosed as mucinous adenocarcinoma. Clinical and radiographic examinations disclosed no evidence of tumor elsewhere. The patient received radiotherapy, but the general condition deteriorated and died 11 months after tumor detection. Thoracic autopsy revealed an anterior mediastinal tumor measuring greater than 10 cm, uncapsulated, and white. The tumor had clear margins and was clearly isolated from the lung. Histologically, the tumor demonstrated papillary, acinar, and cribriform structure and produced abundant extracellular mucin. Immunohistochemically, most tumor cells were positive for cytokeratin 7, were partially positive for CD5, and were negative for TTF-1, Sp-A, CDX-2, MUC2, napsin A, and cytokeratin 20. Collectively, the diagnosis of the tumor was primary mucinous adenocarcinoma of the thymus. We propose that the mucinous subtype should be recognized as one of the histopathological entities of thymic adenocarcinoma.Entities:
Mesh:
Substances:
Year: 2005 PMID: 15754301 DOI: 10.1016/j.humpath.2004.11.008
Source DB: PubMed Journal: Hum Pathol ISSN: 0046-8177 Impact factor: 3.466