Abstract |
In reviewing the radiographs of 102 patients with known sickle cell anemia, a 7% incidence (seven patients) of severe long-bone sclerosis was found. Of the affected patients 50% had homozygous sickle cell (SS) disease and 50% had sickle cell- hemoglobin C (SC) or S- thalassemia disease. No distinguishing radiographic features were found between these two groups. Those patients with SS disease and long-bone sclerosis were younger, had lower hemoglobin levels, and many more hospital admissions than those with SC or S- thalassemia disease and long-bone sclerosis. A review of the medical charts of these osteosclerotic patients with SS disease showed a probable positive correlation between infarctive episodes and hospital admissions in these patients. Therefore, patients with SS disease and severe long-bone sclerosis are seen much more frequently by the radiologist than those with SC or S- thalassemia and long-bone changes. These observations help negate any impression that severe long-bone sclerosis occurs frequently in and has a predilection for patients with homozygous SS disease.
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Authors | S Weinberg |
Journal | Radiology
(Radiology)
Vol. 145
Issue 1
Pg. 41-3
(Oct 1982)
ISSN: 0033-8419 [Print] United States |
PMID | 7122892
(Publication Type: Journal Article)
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Topics |
- Adolescent
- Adult
- Aged
- Anemia, Sickle Cell
(complications, diagnosis, diagnostic imaging)
- Female
- Femur
(diagnostic imaging)
- Fibula
(diagnostic imaging)
- Humans
- Humerus
(diagnostic imaging)
- Male
- Middle Aged
- Osteosclerosis
(diagnostic imaging)
- Radiography
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