Guidelines for the diagnosis and management of hereditary spherocytosis – 2011 update

שנת פרסום ראשונה: 2004
שנת עדכון: נובמבר 2011
מפרסם: British Journal of Haematology

Guidelines on hereditary spherocytosis (HS) published in 2004 (Bolton-Maggs et al, 2004) are here replaced to reflect changes in current opinion on the surgical management, (particularly the indications for concomitant splenectomy
with cholecystectomy in children with mild HS, and concomitant cholecystectomy with splenectomy in those with asymptomatic gallstones). Further potential long term
hazards of splenectomy are now recognised. Advances have been made in our understanding of the biochemistry of the red cell membrane which underpins the choice of tests. Biochemical assays of membranes proteins and genetic analysis may be indicated (rarely) to diagnose atypical cases. The diagnostic value of the eosin-5-maleimide (EMA) binding test has been validated in a number of studies with
understanding of its limitations.

British Journal of Haematology, 156, 37–49,  doi:10.1111/j.1365-2141.2011.08921.x