Results 271 to 280 of about 4,455,205 (312)

SUBHYALOID HEMORRHAGE IN EVANS SYNDROME

RETINAL Cases & Brief Reports, 2023
Purpose: Evans syndrome is a rare disorder characterized by autoimmune hemolytic anemia and immune thrombocytopenia. We report the first case of ophthalmic involvement in a pediatric patient with Evans syndrome, in which painless vision loss was the presenting symptom.
Georges I. Guillaume, Bliss E. O'Bryhim, Surbhi Saini, Gregg T. Lueder   +3 more
openaire   +2 more sources

Evans Syndrome

Journal of Pediatric Hematology/Oncology, 1997
Our goal was to improve the management of Evans Syndrome, an uncommon and frequently refractory condition. We conducted a retrospective survey to assess the demography, presentation, clinical course, and treatment response of affected children.Information was analyzed from a detailed questionnaire completed by pediatric hematologists mainly in the U.S.
P, Mathew, G, Chen, W, Wang
openaire   +2 more sources

Familial autoimmunity and risk of developing immune thrombocytopenia and Evans syndrome

Pediatric Blood & Cancer
Immune thrombocytopenia (ITP) and Evans syndrome (ES) are manifestations of immune dysregulation. Genetic variants in immune‐related genes have been identified in patients with ITP and especially ES.
Michell M. Lozano Chinga, J. Bussel, M. Fluchel, Jacob Wilkes, Chong Zhang, Huong D. Meeks, J. Meznarich   +6 more
semanticscholar   +1 more source

Refractory autoimmune cytopenias in pediatric Evans syndrome with underlying systemic immune dysregulation

European Journal of Haematology, 2021
Evans syndrome is a rare but challenging disorder in children; and despite rapidly growing evidence for targetable systemic immune dysregulation driving these “idiopathic” autoimmune cytopenias, precision diagnosis and management remains sub‐optimal ...
Amanda B. Grimes, T. Kim, Susan E. Kirk, Jonathan M. Flanagan, Michele P. Lambert, R. Grace, J. Despotovic   +6 more
semanticscholar   +1 more source

Pediatric Evans syndrome is associated with a high frequency of potentially damaging variants in immune genes.

Blood, 2019
Evans syndrome (ES) is a rare severe autoimmune disorder characterized by the combination of autoimmune hemolytic anemia and immune thrombocytopenia. In most cases, the underlying cause is unknown.
J. Hadjadj, N. Aladjidi, H. Fernandes, G. Leverger, A. Magerus-Chatinet, F. Mazerolles, M. Stolzenberg, Sidonie Jacques, C. Picard, J. Rosain, C. Fourrage, S. Hanein, M. Zarhrate, M. Pasquet, Wadih Abou Chahla, V. Barlogis, Y. Bertrand, I. Pellier, Elodie Colomb Bottollier, F. Fouyssac, P. Blouin, C. Thomas, N. Cheikh, E. Doré, C. Pondarré, D. Plantaz, E. Jeziorski, F. Millot, N. Garcelon, S. Ducassou, Y. Pérel, T. Leblanc, B. Neven, A. Fischer, F. Rieux-Laucat   +34 more
semanticscholar   +1 more source

Laparoscopic Splenectomy for Evans Syndrome

Surgical Laparoscopy, Endoscopy & Percutaneous Techniques, 2003
Evans syndrome is a rare, chronic, sometimes fatal immunologic disorder defined as Coombs' positive hemolytic anemia and immune thrombocytopenia without an underlying etiology. This syndrome has a variable clinical course, and the benefit of splenectomy is unknown. This report reviews the clinical outcome of laparoscopic splenectomy for Evans syndrome.
Terive, Duperier, Joshua, Felsher, Fred, Brody   +2 more
openaire   +2 more sources

Pregnancy complicated by Evan’s syndrome

European Journal of Obstetrics & Gynecology and Reproductive Biology, 2001
Evan's syndrome was initially diagnosed in a 26-year-old pregnant patient. Following the introduction of high dose steroid therapy, the patient developed possible disseminated gonococcal infection which was followed by preterm labor and abruptio placentae.
Z, Selçuk Tuncer, Y, Büyükaşik, E, Demirtaş, R, Tuncer, P, Zarakolu   +4 more
openaire   +2 more sources

Familial Evans Syndrome

Journal of Pediatric Hematology/Oncology, 1999
This report describes the clinical course of three siblings, all of whom had Evans syndrome in childhood.The coexistence of autoimmune hemolytic anemia and thrombocytopenia, in the absence of a known underlying cause, led to the diagnosis of Evans syndrome in a 4-month-old girl and subsequently in her two brothers when they were 4 and 13 years old.The ...
A G, McLeod, M, Pai, R F, Carter, J, Squire, R D, Barr   +4 more
openaire   +2 more sources

Evans’ syndrome induced by atezolizumab plus bevacizumab combination therapy in advanced hepatocellular carcinoma

Clinical Journal of Gastroenterology, 2023
Masanori Fukushima, K. Tajima, R. Sasaki, Yasuhiko Nakao, Kosuke Takahashi, E. Ozawa, Satoshi Miuma, Takeharu Kato, Hisamitsu Miyaaki, K. Nakao   +9 more
semanticscholar   +1 more source

Evans Syndrome

Journal of Turgut Ozal Medical Center, 2013
Roxana Ghashghaei, Remus Popa, John Shen
openaire   +2 more sources