| Literature DB >> 19797831 |
Atsushi Kitamura1, Yuichi Takiguchi, Naobumi Tochigi, Shun-ichi Watanabe, Seiichirou Sakao, Katsushi Kurosu, Nobuhiro Tanabe, Koichiro Tatsumi.
Abstract
Good syndrome, characterized by hypogammaglobulinemia and acquired immunodeficiency, is a rare condition associated with thymoma. A 67-year-old woman, who 4 months previously had a thymoma resected, presented with generalized hypogammaglobulinemia with a severely decreased B cell population as demonstrated by flow cytometry. She was diagnosed as having bacterial mediastinitis associated with Good syndrome. For the subsequent 6 years, she suffered from repeated serious bacterial infections. As this paraneoplastic syndrome is not resolved by tumor removal, careful management with intensive infection-control using antibiotics and intravenous immunoglobulins is required for the long term. Serum immunoglobulin levels should be evaluated for patients with thymoma and suspected vulnerability to infection.Entities:
Mesh:
Year: 2009 PMID: 19797831 DOI: 10.2169/internalmedicine.48.2375
Source DB: PubMed Journal: Intern Med ISSN: 0918-2918 Impact factor: 1.271