Results 131 to 140 of about 21,508 (259)

Catastrophic Antiphospholipid Syndrome in a Young Female Complicated by Systemic Lupus Erythematosus and Left Atrial Myxoma: A Rare Case Report

open access: yesClinical Case Reports, Volume 14, Issue 6, June 2026.
ABSTRACT Catastrophic antiphospholipid syndrome (CAPS) is a fulminant and rare variant of antiphospholipid syndrome characterized by rapidly progressive multiorgan thrombosis and a high mortality rate. Its diagnosis is often challenging due to overlapping clinical features with sepsis, thromboembolic disorders, and systemic autoimmune diseases.
Nazmin Ahmed   +4 more
wiley   +1 more source

A case of cephalosporin-induced autoimmune hemolytic anemia

open access: yes, 2006
Drug-induced autoimmune hemolytic anemia is a quite rare state in childhood. Currently, most of the reported cases of drug-induced hemolytic anemia are those caused by the second and third generation cephalosporins. In this paper, an infant who developed
Polat, Aziz   +5 more
core  

Tolosa-Hunt syndrome in a patient with autoimmune hemolytic anemia.

open access: yes, 2010
Tolosa-Hunt syndrome is a steroid responsive painful opthalmoplegia due to a nonspecific inflammation of the cavernous sinus. Autoimmune hemolytic anemia is caused by antibodies directed against unmodified autologous red cells.
Andrea Elefante   +9 more
core   +1 more source

Pancytopenia With Hypocellular Bone Marrow Revealing Extrahepatic Portal Venous Obstruction and Cavernous Transformation in a Child: A Case Report of a Diagnostic Challenge

open access: yesClinical Case Reports, Volume 14, Issue 6, June 2026.
ABSTRACT Extrahepatic portal venous obstruction (EHPVO) is a leading cause of prehepatic portal hypertension in children, particularly in developing countries. While upper gastrointestinal bleeding is the most common presentation, EHPVO may rarely manifest predominantly with hematological abnormalities due to hypersplenism, posing a diagnostic ...
Swekchha Adhikari   +6 more
wiley   +1 more source

Autoimmune hemolytic anemia with negative Coombs test [PDF]

open access: yes, 2017
Introduction: autoimmune hemolytic anemia is a type of low-grade acquired hemolytic anemia, produced by antibodies against the patient's own erythrocytes leading to their destruction.   Case report: a 12 year-old female patient arrived in the emergency
Juan Manuel Acosta Piloto   +1 more
core  

EHA Guidelines on management of chronic lymphocytic leukemia and Richter transformation

open access: yesHemaSphere, Volume 10, Issue 6, June 2026.
Abstract Previous editions of the European guidelines for the management of chronic lymphocytic leukemia (CLL) were developed by experts in CLL under the auspices of the European Society for Medical Oncology (ESMO). These previous editions have served as a reference text for many physicians caring for patients with CLL.
Barbara Eichhorst   +13 more
wiley   +1 more source

Maternal and Neonatal Outcomes of Immune Thrombocytopenia in Pregnancy: A Five‐Year Single‐Center Cross‐Sectional Study

open access: yesHealth Science Reports, Volume 9, Issue 6, June 2026.
ABSTRACT Objectives Immune thrombocytopenia (ITP) during pregnancy presents unique management challenges. This study represents the first analysis of ITP outcomes during pregnancy in Qatar, aiming to assess maternal and neonatal outcomes at a tertiary care center.
Sara Elkorashi   +10 more
wiley   +1 more source

Opinion: Presumable Reason of Interrelationship between Autoimmune Hemolytic Anemia and Cancer Arising

open access: yes, 2015
The mechanism of malignant transformation in autoimmune hemolytic anemia can be based on the inclusion of immunocompetent cells in different cellular cooperations.
Gogichadze, G.K.; Tbilisi State Medical University
core  

Reappraisal of the etiology of extracorpuscular non-autoimmune acquired hemolytic anemia in 2657 hospitalized patients with non-neoplastic disease

open access: yes, 2014
[[abstract]]INTRODUCTION: Unlike autoimmune hemolytic anemia (AIHA), literature on the etiological study of non-autoimmune hemolytic anemia (non-AIHA) is scarce. The incidence and prevalence of non-AIHA in different geographic regions are largely unknown
Victor C Kok;郭集慶;Chien-Kuan Lee;Jorng-Tzong Horng;洪炯宗;Che-Chen Lin;Fung-Chang Sung
core  

Luspatercept in Transfusion‐Dependent Thalassemia With Red Blood Cell Antibodies: A Case Series

open access: yeseJHaem, Volume 7, Issue 3, June 2026.
ABSTRACT Red blood cell (RBC) antibodies complicate transfusion support in transfusion‐dependent thalassemia (TDT), and data on luspatercept in this setting remain limited. We retrospectively reviewed seven adults with TDT and RBC antibodies treated with luspatercept at Srinagarind Hospital from January 2025 to January 2026.
Nattiya Teawtrakul
wiley   +1 more source

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