Title of article
Spinal cord compression secondary to extramedullary hematopoiesis: a rareness in a young adult with thalassemia major
Author/Authors
Fareed, Shehab Oncology and Hematology Department - National Center for Cancer Care and Research (NCCCR) - Hamad Medical Corporation (HMC), Doha, Qatar , Soliman, Ashraf Alexandria University Children’s Hospital, Elchatby, Alexandria, Egypt , De Sanctis, Vincenzo Pediatric and Adolescent Outpatient Clinic - Quisisana Hospital, Ferrara, Italy , Kohla, Samah Department of Lab Med and Pathology - National Center for Cancer Care and Research (NCCCR) - Hamad Medical Corporation (HMC), Doha, Qatar , Soliman, Dina Department of Lab Med and Pathology - National Center for Cancer Care and Research (NCCCR) - Hamad Medical Corporation (HMC), Doha, Qatar , Khirfan, Diala Oncology and Hematology Department - National Center for Cancer Care and Research (NCCCR) - Hamad Medical Corporation (HMC), Doha, Qatar , Tambuerello, Adriana Polyclinic University Hospital, Palermo, Italy , Talaat, Mohamed Radiology Department - Hamad Medical Corporation (HMC), Doha, Qatar , Nashwan, Abdulqadir Oncology and Hematology Department - National Center for Cancer Care and Research (NCCCR) - Hamad Medical Corporation (HMC), Doha, Qatar , Caparrotti, Palmira Oncology and Hematology Department - National Center for Cancer Care and Research (NCCCR) - Hamad Medical Corporation (HMC), Doha, Qatar , Yassin, Mohamed A. Oncology and Hematology Department - National Center for Cancer Care and Research (NCCCR) - Hamad Medical Corporation (HMC), Doha, Qatar
Pages
6
From page
237
To page
242
Abstract
We report a case of a thalassemia major male patient with back pain associated to severe weakness in lower extremities resulting in the ability to ambulate only with assistance. An urgent magnetic resonance imaging (MRI) of thoracic and lumbosacral spine was requested. A posterior intraspinal extradural mass lesion compressing the spinal cord at the level of thoracic T5-8 was present, suggesting an extramedul-lary hematopoietic centre, compressing the spinal cord. The patient was treated with blood transfusion, dexamethasone, morphine and paracetamol, followed by radiotherapy in 10 fractions to the spine (daily fraction of 2Gy from T3 to T9, total dose 20 Gy). His pain and neurologic examination quickly improved. A new MRI of the spine, one week after radiotherapy, showed an improvement of the extramedullary he-matopoietic mass compression. In conclusion, EMH should be considered in every patient with ineffective erythropoiesis and spinal cord symptoms. MRI is the most effective method of demonstrating EMH. The rapid recognition and treatment can dramatically alleviate symptoms. There is still considerable controversy regarding indications, benefits, and risks of each of modality of treatment due to the infrequency of this disorder. (www.actabiomedica.it)
Keywords
extramedullary hematopoiesis , spinal cord compression , thalassemia major , radiotherapy
Journal title
Acta bio-medica : Atenei Parmensis
Serial Year
2017
Record number
2624010
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