Thursday, February 28, 2019

Splenic sequestration crisis

It's gonna be awesome: added Category:Spleen (anatomy) using HotCat


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'''Splenic sequestration crisis''' (SSC) is a life-threatening illness common in pediatric patients with homozygous [[sickle cell disease]] and [[beta thalassemia]]. Up to 30% of these children may develop SSC with a mortality rate of up to 15%. This crisis occurs when splenic [[vessel occlusion|vaso-occlusion]] causes a large percentage of total [[blood volume]] to become trapped within the [[spleen]]. Clinical signs include severe, rapid drop in [[hemoglobin]] leading to [[hypovolemic shock]] and death. Pediatric patients with sickle cell disease and beta thalassemia experience multiple [[splenic infarct]]s, resulting in splenic [[fibrosis]] and [[scarring]]. Over time, this leads to a small, auto infarcted spleen typically by the time patients reach adulthood. Splenic sequestration crisis can only occur in functioning spleens which may be why this crisis is rarely seen in adults. However, late adolescent or adult patients in this group who maintain splenic function may develop splenic sequestration crisis. <ref name="Chapman Azevedo 2018 p. ">, [[Tertiary source]]}}</ref>

==Reference==




[[Category:Spleen (anatomy)]]


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