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一名患有青少年强直性脊柱炎、特发性血小板减少性紫癜和α地中海贫血的患者出现骨软骨瘤。

Osteochondroma in a patient with juvenile ankylosing spondylitis associated with idiopathic thrombocytopenic purpura and alpha thalassemia.

作者信息

Tsai C Y, Yu C L, Tsai Y Y, Wu T H, Tsai S T

机构信息

Section of Allergy, Immunology & Rheumatology, Veterans General Hospital-Taipei, Taiwan, ROC.

出版信息

Scand J Rheumatol. 1996;25(1):61-2. doi: 10.3109/03009749609082671.

Abstract

An unusual combination of osteochondroma, ankylosing spondylitis, thalassemia alpha, and thrombocytopenia was found in a young man who had once been an amphetamine addict. The association of these settings might have been coincidental but it cannot be excluded that the preexisting inflammatory processes or tissue destruction in the latter 3 diseases might have rendered the patient prone to the development of osteochondroma.

摘要

在一名曾是苯丙胺成瘾者的年轻男性中,发现了骨软骨瘤、强直性脊柱炎、α地中海贫血和血小板减少症的不寻常组合。这些情况的关联可能是巧合,但不能排除后三种疾病中预先存在的炎症过程或组织破坏可能使患者易于发生骨软骨瘤。

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