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PubMed · 626559

Splenic sequestration with sickle cell-C disease.

F Geola·S C Kukreja·S G Schade
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Abstract

During an episode of pneumonia and multiple pulmonary thromboembolic events, an adult male patient with sickle cell-C hemoglobinopathy developed a severe anemia associated with rapidly increasing splenic size and diminished splenic uptake of technetium Tc 99m sulfur colloid, indicating diminished splenic function due to hypersequestration, a rare and noteworthy phenomenon in adult patients with sickle cell-C disease.

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Acute DiseaseAdultHemoglobin C DiseaseHumansHypersplenismLiverMalePneumonia, PneumococcalPulmonary EmbolismRadionuclide ImagingSpleenSplenomegalyCase ReportsJournal Article

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F Geola, S C Kukreja, S G Schade. 1978. Splenic sequestration with sickle cell-C disease.. https://pubmed.ncbi.nlm.nih.gov/626559/

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