Among adults with S/C sickle cell disease, over 50% have splenomegaly and t
he remainder have asplenia secondary to repeated splenic infarctions during
childhood. Splenic infarction and/or sequestration can occur in adults wit
h S/C sickle cell disease. However, there have been few reports of acute sp
lenic complications in these patients. Published series have been very smal
l, and in many cases the infarction was secondary to severe hypoxia. The ca
se of a young, apparently healthy man who developed splenic infarction as t
he first manifestation of S/C sickle cell disease is reported. He had no hi
story of exposure to high altitudes.