نتایج جستجو برای: castleman syndrome
تعداد نتایج: 622563 فیلتر نتایج به سال:
Abstract Introduction/Objective TAFRO syndrome (thrombocytopenia, anasarca, fever, reticulin fibrosis, and organomegaly) is a rare systemic inflammatory disorder. First reported in 2010, the majority of cases are from Japan, where it currently regarded as subtype HHV8-negative Multicentric Castleman Disease. Methods/Case Report We report case occurring 17-year old Puerto Rico. She originally pr...
Results Among 960 cases fulfilled the definition. 828 (86%) were diagnosed as having diseases of known causes. 190 (23%) were infectious diseases (acute focal bacterial nephritis 31, cat-scratch disease 23, urinary tract infection 20, osteomyelitis 9 and tuberculosis 8), 447 (54%) were rheumatic diseases (JIA 221, vasculitis syndrome 39, inflammatory bowel diseases 34, SLE 25, and MCTD 12), 67 ...
BACKGROUND Castleman's disease or angiofollicular lymphoid hyperplasia is a rare benign lymph node hyperplasia usually presenting as an asymptomatic mediastinal mass in children. The disease can present at any extra thoracic site with lymphoid tissue such as retroperitoneal, mesentery, axilla, and pelvis. Hepatic localization castleman disease is very rare in children. Herein, we reported a cas...
OBJECTIVES Programmed death-1 (PD-1) is physiologically expressed by germinal center (GC)-associated helper T cells. It has been proposed that an increase in PD-1+ cells outside GC could indicate pattern I angioimmunoblastic T-cell lymphoma (AITL). METHODS We studied the distribution of PD-1+ cells in reactive lymphadenopathies (LA), including HIV-associated and dermatopathic LA (n = 5, each)...
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