Results 21 to 30 of about 508 (119)
Good’s Syndrome: Time to Move on From Reviewing the Past [PDF]
Frontiers in Immunology, 2022 For seven decades, the pathophysiology of Good’s syndrome (GS) has remained a mystery, with few attempts to solve it. Initially described as an association between hypogammaglobulinemia and thymoma, controversy exists whether this is a unique disease, or
Aunonna Kabir +4 more
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Significant decreased CXCR3+ phenotype Tfh1 cells in three Good’s syndrome patients [PDF]
Frontiers in ImmunologyBackgroundGood’s syndrome (GS) is a rare acquired immunodeficiency defined by the co-occurrence of thymoma and hypogammaglobulinemia. Follicular helper T (Tfh) cells, a specialized CD4+ T cell subset, play a critical role in supporting B-cell antibody ...
Yanxia Chen +5 more
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B cell deficiency in thymoma tissues of Good’s syndrome patients [PDF]
Discover OncologyObjectives Good’s syndrome (GS) is a rare secondary immunodeficiency which is characterized by hypogammaglobulinemia and thymoma. This study aims to investigate the expression and distribution of B cells in thymoma tissue, given that B cells had been ...
Junwu Zhang +4 more
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Relapsing cellulitis associated with Campylobacter coli bacteremia in a Good’s syndrome patient: a case report [PDF]
BMC Infectious Diseases, 2022 Background Good’s syndrome (GS) is characterized by immunodeficiency, and patients diagnosed with GS are susceptible to infection or even bacteremia, which is the most evident complication. Campylobacter coli (C.
Lei Jiang, Jia Gao, Pu Wang, Yuliang Liu
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Good's syndrome: Thymoma with hypogammaglobulinaemia. [PDF]
Indian J Med Res, 2020 Mathew A, Chengappa KG.
europepmc +3 more sources
Humoral Immunity in Bronchiectasis: Finding Good’s Syndrome [PDF]
Case Reports in Pulmonology, 2015 We present a case of a 37-year-old man with a past history of a surgically removed thymoma, who presented with recurrent pulmonary infections and bronchiectasis. On further testing, he was found to have low total immunoglobulin levels, a constellation of
C. Pu, S. Sukhal, S. Fakhran
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A Rare Complication of Thymoma: Pure White Cell Aplasia in Good’s Syndrome [PDF]
Case Reports in Hematology, 2019 Pure white cell aplasia (PWCA) is a rare manifestation of thymoma. It is characterized by agranulocytosis with absent myeloid precursors in the bone marrow and normal hematopoiesis for other cell lines.
Kim Uy +4 more
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Good Syndrome, Bad Problem [PDF]
Frontiers in Oncology, 2014 Good syndrome (GS), which is classically defined as the triad of thymoma, immunodeficiency, and hypogammaglobulinemia, was first characterized by Robert Alan Good, a pioneer in the field of immunodeficiency diseases, who recognized the crucial role that the thymus plays in the development of the immune system (1).
Martinez, Bianca, Browne, Sarah K.
openaire +3 more sources
Good’s syndrome with increasing γδ T-lymphocyte subpopulation: A case report [PDF]
Vojnosanitetski Pregled, 2015 Introduction. Good’s syndrome is a rare cause of adultonset immunodeficiency associated with thymoma. Good’s syndrome should be considered in patients older than 40 years with the history of frequent infections.
Tadić Dragana +3 more
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Good's Syndrome with Pneumocystis Jiroveci Lymphadenitis and Pure Red Cell Aplasia [PDF]
Journal of Microbiology and Infectious Diseases, 2016 Pneumocystis jiroveci lymphadenitis is a rare manifestation of extrapulmonary pneumocystosis. A case of recurrent infection with lymphadenitis caused by Pneumocystis jiroveci in a middle-aged patient is described.
Jintana - Srisompong, Torpong - Thongngarm, Popchai - Ngamskulrungroj, Ruchira - Ruangchira-urai, Adhiratha - Boonyasiri
doaj +1 more source