Cargando…
Prevalence of Splenomegaly and Splenic Complications in Adults with Sickle Cell Disease and Its Relation to Fetal Hemoglobin
Background: Spleen has been found to be the earliest organ involved in sickle cell disease (SCD) patients with variable manifestations in different geographical regions. It usually undergoes autosplenectomy by adolescence but in countries like India, the course of the disease and splenic manifestati...
Autores principales: | Lakhani, Jitendra D, Gill, Rooppreet, Mehta, Deep, Lakhani, Sucheta J |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Tehran University of Medical Sciences, Hematology-Oncology and Stem Cell Transplantation Research Center
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9985811/ https://www.ncbi.nlm.nih.gov/pubmed/36883109 http://dx.doi.org/10.18502/ijhoscr.v16i4.10877 |
Ejemplares similares
-
Sickle Cell Disease and Fetal Hemoglobin
por: Rivera, Alicia
Publicado: (2018) -
Laparoscopic splenectomy in an elderly patient with splenic limphoma and splenomegaly
por: Antonelli, G, et al.
Publicado: (2010) -
Fetal hemoglobin and hemolysis markers in sickle cell anemia()
por: Colella, Marina Pereira, et al.
Publicado: (2015) -
Fever, anemia, and splenomegaly: A rare presentation of splenic angiosarcoma
por: Shukla, Mridula, et al.
Publicado: (2011) -
Palliative splenic irradiation for symptomatic splenomegaly in non-Hodgkin lymphoma
por: Oliveira, Liliana Castro, et al.
Publicado: (2018)