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[A case of asplenia in a sickle cell homozygote SS patient]
K P N'Zi1, K N'Dri, D N Ouattara
1Service de radiologie, C.H.U. de Treichville, Abidjan, Côte d'Ivoire.
Bulletin De La Societe De Pathologie Exotique (1990)
|June 27, 1998
Abstract:
One case of total splenic atrophy is reported in a patient with SS homozygous sickle-cell disease presenting no related malformation, thus recalling the IVEMARK syndrome. An abdominal echography and computed tomography are indispensable in order to confirm the absence of the anatomic spleen; this makes for a better follow-up of sickle-cell disease.