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Asian Cardiovasc Thorac Ann ; 25(2): 146-149, 2017 Feb.
Article in English | MEDLINE | ID: mdl-28068785

ABSTRACT

Good's syndrome or thymoma-associated immunodeficiency is a rare clinical entity that is often presumed to be common variable immunodeficiency, due to lack of awareness and recognition of this syndrome. This syndrome more often goes unrecognized if a thymoma is not detected. An appropriate immunological work-up that aids timely diagnosis and adequate therapy with antimicrobials and intravenous immunoglobulins are mandatory to prevent the long-term complications and mortality associated with this syndrome. We present the clinical and immunological profile of a young man with Good's syndrome that was initially presumed to be common variable immunodeficiency.


Subject(s)
Agammaglobulinemia/diagnosis , Common Variable Immunodeficiency/diagnosis , Thymoma/diagnosis , Thymus Neoplasms/diagnosis , Agammaglobulinemia/immunology , Agammaglobulinemia/therapy , Anti-Infective Agents/therapeutic use , Common Variable Immunodeficiency/immunology , Diagnostic Errors , Humans , Immunoglobulins, Intravenous/therapeutic use , Magnetic Resonance Imaging , Male , Middle Aged , Predictive Value of Tests , Syndrome , Thymectomy , Thymoma/complications , Thymoma/immunology , Thymoma/surgery , Thymus Neoplasms/complications , Thymus Neoplasms/immunology , Thymus Neoplasms/surgery , Tomography, X-Ray Computed , Treatment Outcome
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