Pitfalls of thrombotic microangiopathies in children: two case reports and literature review

A Mocanu, RA Bogos, TI Lazaruc, AL Cianga, VV Lupu… - Diagnostics, 2023 - mdpi.com
Thrombotic microangiopathy can present itself in the form of several clinical entities,
representing a real challenge for diagnosis and treatment in pediatric practice. Our article …

The Rationale of Complement Blockade of the MCPggaac Haplotype following Atypical Hemolytic Uremic Syndrome of Three Southeastern European Countries with …

D Turudic, D Pokrajac, V Tasic, D Kasumovic… - International Journal of …, 2023 - mdpi.com
We present eight cases of the homozygous MCPggaac haplotype, which is considered to
increase the likelihood and severity of atypical hemolytic uremic syndrome (aHUS) …

Case report: Autoimmune hemolytic anemia caused by warm and cold autoantibodies with complement activation—etiological and therapeutic issues

D Turudic, S Dejanovic Bekic, L Mucavac… - Frontiers in …, 2023 - frontiersin.org
Introduction Research on mixed warm and cold autoantibodies in autoimmune hemolytic
anemia (AIHA) targeting erythrocytes [red blood cells (RBCs)] and platelets is scarcely …

Efficacy and Safety of Eculizumab in Enteroaggregative E. coli Associated Hemolytic Uremic Syndrome

R Acharya, WL Clapp, K Upadhyay - Pediatric Reports, 2024 - mdpi.com
Background. Hemolytic uremic syndrome (HUS) may present atypically without the full triad
of classical HUS. Eculizumab has been shown to be efficacious in complement-mediated …

[PDF][PDF] Pitfalls of Thrombotic Microangiopathies in Children: Two Case Reports and Literature Review. Diagnostics 2023, 13, 1228

A Mocanu, RA Bogos, TI Lazaruc, AL Cianga, VV Lupu… - 2023 - academia.edu
Thrombotic microangiopathy can present itself in the form of several clinical entities,
representing a real challenge for diagnosis and treatment in pediatric practice. Our article …