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. © 2009 The Japanese Society of Internal Medicine.
CITATION STYLE
Kitamura, A., Takiguchi, Y., Tochigi, N., Watanabe, S. I., Sakao, S., Kurosu, K., … Tatsumi, K. (2009). Durable hypogammaglobulinemia associated with thymoma (Good syndrome). Internal Medicine, 48(19), 1749–1752. https://doi.org/10.2169/internalmedicine.48.2375
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