Splenic structural and functional abnormalities in individuals with NR5A1/SF-1 variants [PDF]
Purpose: Steroidogenic factor 1 (SF-1), encoded by NR5A1, is essential for spleen development and function. NR5A1 variants have been linked to abnormal spleen development.
Khadidja Fouatih +18 more
doaj +3 more sources
Autosplenectomy in a Patient With Autoimmune Polyglandular Syndrome Type 2 (APS-2) [PDF]
Autoimmune glandular syndrome type 2 is a complex genetic condition where a triad of endocrinopathies is involved, namely, Addison’s disease, type 1 diabetes, and/or autoimmune thyroid disorder.
Luqman S. Fauzi +3 more
doaj +3 more sources
Impaired IgM Memory B Cell Function Is Common in Coeliac Disease but Conjugate Pneumococcal Vaccination Induces Robust Protective Immunity [PDF]
Coeliac disease (CD) is associated with hyposplenism, an acquired impairment of spleen function associated with reduced IgM memory B cells and increased susceptibility to serious pneumococcal infection.
Olivia G. Moscatelli +11 more
doaj +4 more sources
Hyposplenism and Gastrointestinal Diseases: Significance and Mechanisms [PDF]
<b><i>Background:</i></b> Functional hyposplenism is a recognized complication of several gastroenterological disorders, including coeliac and inflammatory bowel diseases, and is believed to contribute to the increased infection risk seen in these disorders.
Abhinav Mathur +3 more
openaire +5 more sources
Hyposplenism as a cause of pneumococcal meningoencephalitis in an adult patient with coeliac disease
Introduction: Coeliac disease can be associated with hyposplenism and splenic atrophy, which may increase the patient’s risk for fatal infections caused by Streptococcus pneumoniae or Pneumococcus.
Paolo Caraceni +5 more
doaj +2 more sources
Epidemiology and Characterization of Immunological Disorders in Children Diagnosed With Pneumococcal Invasive Disease. [PDF]
Aim A substantial proportion of children hospitalized with invasive pneumococcal infection are subjected to immune evaluations, to detect immunological disorders (ID). The literature lacks thorough analysis of the necessity and effectiveness of these evaluations for previously healthy children with such infections.
Shahar C +3 more
europepmc +2 more sources
Dextrocardia in Heterotaxy Syndrome (Polysplenia Variant) in a 36-Year-Old Ethiopian Woman: A Case Report and Literature Review. [PDF]
Background Heterotaxy syndrome—polysplenia variant (left isomerism) with dextrocardia is a rare constellation of laterality defects characterized by left‐isomerism, multiple splenic nodules, and associated vascular and visceral anomalies. This report describes an adult Ethiopian woman who presented with nonspecific abdominal pain and was found to have ...
Tukeni KN +5 more
europepmc +2 more sources
Hyposplenism in systemic lupus erythematosus: biological and radiological characteristics and its association with increased risk of infection [PDF]
Objective This study aimed to evaluate the prevalence of hyposplenism in patients with systemic lupus erythematosus (SLE) and its association with an increased risk of infection.Methods This single-centre study included patients with SLE who underwent a ...
Zahir Amoura +13 more
doaj +2 more sources
Underrecognised Functional Hyposplenism Associated With Chronic Graft‐Versus‐Host Disease: A Case Report [PDF]
eJHaem, Volume 6, Issue 2, April 2025.
Kaori Uchino +17 more
doaj +3 more sources
Protein S Enhances the Phagocytosis of Phosphatidylserine-Exposing Erythrocytes: Implications in Sickle Cell Disease. [PDF]
ABSTRACT The major anticoagulant Protein S (PROS1) also contributes to the phagocytosis of apoptotic cells by bridging exposed phosphatidylserine (PtdSer) to the MerTK receptor on macrophages (efferocytosis). Whether PROS1 is involved in the splenic clearance of PtdSer‐positive senescent and altered erythrocytes such as erythrocyte ghosts (eryghosts ...
Auditeau C +26 more
europepmc +2 more sources

