Cortical bone invasion in non-transfusion-dependent thalassemia: tumefactive extramedullary hematopoiesis reviewed

dc.contributor.authorMasrouha, Karim Z.
dc.contributor.authorWazen, Joelle
dc.contributor.authorHaddad, Anthony G.
dc.contributor.authorSaadeh, Fadi
dc.contributor.authorTaher, Ali T.
dc.contributor.authorKhoury, Nabil El
dc.contributor.departmentSurgery
dc.contributor.departmentDiagnostic Radiology
dc.contributor.departmentInternal Medicine
dc.contributor.departmentDivision Of Orthopedic Surgery
dc.contributor.departmentDivision of Hematology Oncology
dc.contributor.facultyFaculty of Medicine (FM)
dc.contributor.institutionAmerican University of Beirut
dc.date.accessioned2025-01-24T12:12:43Z
dc.date.available2025-01-24T12:12:43Z
dc.date.issued2016
dc.description.abstractObjective of the study: To assess the prevalence of cortical bone invasion (CBI) with secondary extramedullary hematopoiesis (EMH) in patients with non-transfusion-dependent thalassemia (NTDT), to determine its predilection sites on thoracic and abdominal imaging, to determine whether there is an association between various clinical and hematological parameters, and to evaluate its various findings mainly on magnetic resonance imaging (MRI), in addition to computed tomography (CT) scans. Materials and methods: This is a retrospective cohort study of 57 patients with NTDT imaged by CT or MRI. Both clinical and laboratory data were gathered. An imaging scoring system was used to describe the appearance of CBI by MRI. Results: Twenty-seven patients (47.4 %) were found to have CBI and EMH with the most common location being the thoracic spine. Splenectomy and lower hemoglobin level were found to be independent risk factors for its development. Most lesions were homogenous (70 %), had predominant red marrow signal (67 %), and well-defined margins (89 %). Conclusion: CBI and secondary tumefactive EMH are common findings in patients with NTDT, with distinct imaging and clinical characteristics. An increased risk was seen in patients with splenectomy and lower hemoglobin. The imaging scoring system described is helpful in diagnosing and describing this entity, hence precluding unnecessary biopsies. © 2016, Italian Society of Medical Radiology.
dc.identifier.doihttps://doi.org/10.1007/s11547-016-0638-1
dc.identifier.eid2-s2.0-84964265107
dc.identifier.pmid27108419
dc.identifier.urihttp://hdl.handle.net/10938/32854
dc.language.isoen
dc.publisherSpringer-Verlag Italia s.r.l.
dc.relation.ispartofRadiologia Medica
dc.sourceScopus
dc.subjectCortical bone invasion
dc.subjectExtramedullary hematopoiesis
dc.subjectNon-transfusion-dependent thalassemia
dc.subjectSoft tissue lesion
dc.subjectAdolescent
dc.subjectAdult
dc.subjectChild
dc.subjectContrast media
dc.subjectCortical bone
dc.subjectFemale
dc.subjectHematopoiesis, extramedullary
dc.subjectHumans
dc.subjectIohexol
dc.subjectMagnetic resonance imaging
dc.subjectMale
dc.subjectMiddle aged
dc.subjectRetrospective studies
dc.subjectRisk factors
dc.subjectThalassemia
dc.subjectTomography, x-ray computed
dc.subjectContrast medium
dc.subjectComplication
dc.subjectDiagnostic imaging
dc.subjectHuman
dc.subjectNuclear magnetic resonance imaging
dc.subjectPathology
dc.subjectRetrospective study
dc.subjectRisk factor
dc.subjectX-ray computed tomography
dc.titleCortical bone invasion in non-transfusion-dependent thalassemia: tumefactive extramedullary hematopoiesis reviewed
dc.typeArticle

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