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Published on: March 14, 2017
The many faces of sickle cell disease in children: complications in the appendicular skeleton
Marcela De La Hoz Polo1, Victoria E Hudson2, John Adu3
1Everlight Radiology, London, UK.
Insights
Sickle cell disease (SCD) causes bone problems in children, including infections and bone death. This review helps radiologists identify these appendicular skeletal complications using imaging.
Area of Science:
- Pediatric Radiology
- Hematology
- Orthopedics
Background:
- Sickle cell disease (SCD) is an inherited red blood cell disorder.
- Musculoskeletal complications are a major source of morbidity in children with SCD.
- Common complications include osteomyelitis, osteoporosis, and osteonecrosis.
Purpose of the Study:
- To familiarize pediatric radiologists with appendicular skeletal complications of SCD.
- To describe the characteristic imaging appearances of these complications.
Main Methods:
- Review of relevant literature and imaging findings in pediatric SCD patients.
- Focus on appendicular skeletal manifestations.
Main Results:
- Detailed description of imaging features for osteomyelitis, osteoporosis, and osteonecrosis in SCD.
- Highlighting key diagnostic indicators for radiologists.
Conclusions:
- Accurate imaging interpretation is crucial for managing SCD-related bone complications in children.
- Radiologists play a vital role in the early diagnosis and management of these conditions.
Abstract:
Sickle cell disease (SCD) is a hereditary red cell disorder with clinical manifestations secondary to sickling or crescent-shaped distortion of the red blood cells. Musculoskeletal complications of SCD are often the main causes for acute and chronic morbidities in children with manifestations including osteomyelitis, osteoporosis and osteonecrosis. This article aims to familiarise the paediatric radiologist with appendicular skeletal complications of SCD in the paediatric population and their imaging appearance.
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