Results 21 to 30 of about 56,879 (225)
Concurrent severe pulmonary tuberculosis with Evans syndrome: a case report with literature review
BMC Infectious Diseases, 2022 Background Tuberculosis is a bacterial infection involving multiple organs and systems. Its hematological presentation mainly includes anemia and leukocytosis.
Xiao-hong Pan +7 more
doaj +1 more source
Hepatology, EarlyView., 2022 Natural history of liver disease in a large international cohort of children with Alagille syndrome: Results from the GALA study. Abstract Background and Aims Alagille syndrome (ALGS) is a multisystem disorder, characterized by cholestasis. Existing outcome data are largely derived from tertiary centers, and real‐world data are lacking.
Shannon M. Vandriel +93 more
wiley +1 more source
BJS (British Journal of Surgery), EarlyView., 2020 Recommendations for clinical and molecular identification of LS, surgical and endoscopic management of LS‐associated colorectal cancer and preventive measures for cancer were produced. The emphasis was on surgical and gastroenterological aspects of the cancer spectrum.
T. T. Seppälä +18 more
wiley +1 more source
SARS-COV-2 infection in a patient with Evans syndrome: A silent enemy or an ally? [PDF]
Vojnosanitetski Pregled, 2020 Introduction. During the current outbreak of Coronavirus disease 2019 (COVID-19), the way to manage patients with autoimmune diseases remains elusive due to limited data available. Case report.
Pantić Nikola +5 more
doaj +1 more source
Evans syndrome in adults: an observational multicenter study [PDF]
Blood Advances, 2021 Abstract Evans syndrome (ES) is a rare condition, defined as the presence of 2 autoimmune cytopenias, most frequently autoimmune hemolytic anemia and immune thrombocytopenia (ITP) and rarely autoimmune neutropenia. ES can be classified as primary or secondary to various conditions, including lymphoproliferative disorders, other systemic ...
Bruno Fattizzo +20 more
openaire +8 more sources
Boletín Médico Del Hospital Infantil de México (English Edition), 2017 Evans syndrome is characterized by the reduction of at least two blood cell lineages in the absence of other diagnoses; it was previously described as the simultaneous or sequential development of autoimmune hemolytic anemia and immune thrombocytopenia with unknown etiology. An incidence of 37% and mortality rate of 10% were reported for Evans syndrome.
Olivia Alejandra, Flores-Montes +3 more
openaire +2 more sources
Indian Journal of Endocrinology and Metabolism, 2013 Evans syndrome is a rare combination of autoimmune hemolytic anemia and immune thrombocytopenia. Their association with autoimmune thyroid diseases has been reported by few authors; however, a sequential development of the Evans syndrome in cases of ...
Kalyan Koti +3 more
doaj +1 more source
Evans syndrome during pembrolizumab therapy for upper urinary tract cancer
IJU Case Reports, 2023 Introduction Immune checkpoint inhibitors are available for the treatment of advanced urothelial carcinoma; however, serious adverse events occasionally occur.
Shota Kakita +8 more
doaj +1 more source
Chronic Lymphocytic Leukaemia Presenting with Pancytopenia: A Rare Haematological Coincidence [PDF]
Journal of Clinical and Diagnostic Research, 2021 Chronic Lymphocytic Leukaemia (CLL) is commonly associated with autoimmune cytopenias but CLL presenting with pancytopenia is a rare occurrence. Here, we present a case of 56-year-old male patient, who presented with pallor, mild hepatosplenomegaly ...
Iffat Jamal +4 more
doaj +1 more source
Haploinsufficiency in PTPN2 leads to early-onset systemic autoimmunity from Evans syndrome to lupus [PDF]
Journal of Experimental MedicineFrédéric Rieux-Laucat +2 more
exaly +2 more sources