Correlation between maxillofacial radiographic features and systemic severity as sickle cell disease severity predictor
- 7 June 2011
- journal article
- Published by Springer Nature in Clinical Oral Investigations
- Vol. 16 (3) , 827-833
Abstract
This study was conducted to investigate the relationship among radiographic features observed on panoramic radiographs of sickle cell disease patients and analyze their relationship with history of systemic severity of the disease. Panoramic radiographs of 71 subjects with sickle cell disease were evaluated for the presence of the following radiographic bony alterations: radiopaque areas, increased spacing of bony trabeculae, horizontal arrangement of bony trabeculae and corticalization of mandibular canal. History of clinical systemic severity was assessed through direct questioning about the frequency of vaso-occlusive crisis, history of stroke, clinical jaundice, femur head necrosis, and leg ulceration. Chi-square or Fisher’s exact test were applied in order to analyze possible associations between radiographic features and history of complications, with p < 0.05 significance level. Increased spacing of bony trabeculae was statistically associated with absence of corticalization of mandibular canal (p < 0.01) and horizontal arrangement of bony trabeculae (p = 0.04). Statistically significant associations were demonstrated between history of clinical jaundice and presence of increased spacing of bony trabeculae (p = 0.02) and between history of stroke and presence of horizontal arrangement of bony trabeculae (p = 0.04). Based on the results of the current study, maxillofacial radiographic features may be associated with clinical parameters of systemic complications in sickle cell disease patients. The relationship between radiographic features and history of complications associated with clinical severity of sickle cell disease has not been demonstrated in the literature. Acknowledgment of such possible association may help establish prognosis and influence clinical treatment of systemic and oral complications.Keywords
This publication has 40 references indexed in Scilit:
- Vasculopathy in sickle cell disease: Biology, pathophysiology, genetics, translational medicine, and new research directionsAmerican Journal of Hematology, 2009
- Magnetic resonance imaging evaluation of mandibular condyle bone marrow and temporomandibular joint disc signal intensity in anaemia patientsDentomaxillofacial Radiology, 2009
- Multifocal Joint Osteonecrosis in Sickle Cell DiseaseThe Open Orthopaedics Journal, 2009
- Dental considerations in the management of children suffering from sickle cell disease: A case reportJournal of Indian Society of Pedodontics and Preventive Dentistry, 2007
- The hematological etiology of osteoporosisMedical Hypotheses, 2006
- Mandibular lesions of vasoocclusive origin in sickle cell hemoglobinopathyOdontology, 2004
- The dental management of children with sickle cell disease and β‐thalassaemia: a reviewInternational Journal of Paediatric Dentistry, 1996
- Diagnosis of acute bone/bone marrow infarction of the mandible in sickle hemoglobinopathyOral Surgery Oral Medicine Oral Pathology Oral Radiology and Endodontology, 1996
- Sickle cell disease: a diagnostic dilemmaInternational Endodontic Journal, 1995
- Avascular necrosis of temporomandibular joint in sickle cell diseaseClinical Rheumatology, 1989