A5041647539- Platelet Disorders and Treatments
- Bladder and Urothelial Cancer Treatments
- Urinary and Genital Oncology Studies
- Polyomavirus and related diseases
- Blood groups and transfusion
- Immunodeficiency and Autoimmune Disorders
- Colorectal Cancer Screening and Detection
- Urological Disorders and Treatments
- Antenna Design and Analysis
- Soft tissue tumors and treatment
- Pituitary Gland Disorders and Treatments
- Full-Duplex Wireless Communications
- Autoimmune Bullous Skin Diseases
- Neuroendocrine Tumor Research Advances
- T-cell and B-cell Immunology
- Melanoma and MAPK Pathways
- Parvovirus B19 Infection Studies
- Cancer Diagnosis and Treatment
- Multiple Myeloma Research and Treatments
- Prostate Cancer Diagnosis and Treatment
- Cancer Genomics and Diagnostics
- Plant Virus Research Studies
- Eosinophilic Disorders and Syndromes
- Immune Cell Function and Interaction
- Cutaneous Melanoma Detection and Management
Hôpital Cardiologique du Haut-Lévêque
2015-2019
Inserm
2019
Université de Bordeaux
2016-2019
Service de la Santé Publique
2018
Centre Hospitalier Universitaire de Bordeaux
2015-2018
Sorbonne Université
2016-2017
Pitié-Salpêtrière Hospital
2016-2017
Histologic and phenotypic analyses of splenectomy samples from 17 patients with common variable immunodeficiency (CVID) showed the following nonspecific, evocative, white-pulp lesions: hyperplasia (WPH) reactive follicles, giant follicles (GFs), marginal zone hyperplasia, periarteriolar T-zone (PATH) and/or granulomas, which enabled us to discern 2 groups: first (n=6) composed WPH without second (n=9) characterized by presence granulomas or WPH. All specimens were Epstein-Barr virus negative...
Immune thrombocytopenia (ITP) is an acquired antibody-mediated disease, for which splenectomy remains a curative treatment. We analyzed histology and phenotypes of ITP-splenectomy specimens from 41 adult patients, with different previous ITP-specific treatments, including B-cell–depleting rituximab (RTX) or not, in attempt to predict success failure on the basis day 56 postoperative platelet counts. RTX-naive ITP-spleen samples, compared those 20-patient control trauma cohort, contained...
Immune thrombocytopenia (ITP) is a rare autoimmune bleeding disorder characterized by increased peripheral immune-mediated platelet destruction and impaired bone-marrow megakaryopoiesis. ITP can be linked to other diseases, lymphoproliferative disorders or chronic infections, especially Helicobacter pylori, hepatitis C virus human immunodeficiency virus. Its association with solid tumours has rarely been reported, mostly lung breast cancers (Krauth et al, 2012), but not cardiac myxoma (CM)....