Splenic calcifications in heterozygote sickle cell patients
- PMID: 10024409
- DOI: 10.1007/s002619900473
Splenic calcifications in heterozygote sickle cell patients
Abstract
A small, fibrotic, and even calcified spleen is the hallmark of homozygote sickle cell disease in adults. Such a condition is very rare in sickle-thalassemia and, to our knowledge, not previously reported in a sickle cell trait. We report two heterozygote sickle cell siblings with splenic calcifications, one sickle cell trait and one sickle-beta+-thalassemia, without any history suggestive of splenic vasooclusive-infarctive crisis.
Comment in
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Sickle-beta-thalassemia and splenic calcification.Abdom Imaging. 2001 Sep-Oct;26(5):557. doi: 10.1007/s00261-001-0062-3. Abdom Imaging. 2001. PMID: 11503099 No abstract available.
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