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Spinal Cord Compression in ThalassemiaReport of 12 Cases and Recommendations for Treatment
Surapol Issaragrisil, MD;
Anong Piankijagum, MD, PhD;
Prawase Wasi, MD, PhD
Arch Intern Med. 1981;141(8):1033-1036.
Abstract
Twelve patients with β0-thalassemia/hemoglobin E disease had spinal cord compression. Ten were male and two female, aged 17 to 40 years. The causes of spinal cord compression presumably were extramedullary hematopoietic masses. This was proved by surgery in two cases. In six cases, myelography demonstrated extradural blockade. In the others, the recurrent nature of the paraparesis and the prompt response to deep x-ray therapy were compatible with cord compression by extramedullary hematopoietic masses. Although spontaneous recovery and disappearance of the neurological signs after blood transfusions were observed, these were slow and uncertain. Deep x-ray therapy led to prompt response with more lasting benefit in all cases and is thus recommended as standard treatment for this complication.
(Arch Intern Med 1981;141:1033-1036)
Author Affiliations
From the Department of Medicine, Faculty of Medicine, Siriraj Hospital, Mahidol University, Bangkok, Thailand.
Footnotes
Accepted for publication June 3, 1980.
Reprint requests to Department of Medicine, Faculty of Medicine, Siriraj Hospital, Mahidol University, Bangkok 7, Thailand (Dr Wasi).
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