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免疫功能低下个体中佩吉特病的非典型表现。病例报告。

An atypical presentation of Paget's disease in an immunocompromised individual. A case report.

作者信息

Sanders W, Bertolo S, Wunder J S, Kandel R, White L, Cialdella L, Ferracini R

机构信息

Musculoskeletal Oncology Unit, Mount Sinai Hospital, University of Toronto, Toronto, Canada.

出版信息

Chir Organi Mov. 1999 Oct-Dec;84(4):375-9.

Abstract

Paget's disease of bone is a localized disorder of bony resorption. The mechanism underlying the development of the disease remains controversial. There is substantial evidence suggesting a genetic basis for Paget's disease in some patients. A viral etiology of Paget's disease has been advocated. A further hypothesis implicating an immunological mechanism for this disease is based on growing evidence reviewed in the text. The presented case showed clinical and X-ray features typical of a very aggressive form of Paget's disease. We hypothesize that the extreme local aggressiveness of this case was secondary to the patient's concomitant immunosuppression due to an extended therapy following renal transplant.

摘要

骨佩吉特病是一种局限性骨吸收障碍疾病。该疾病发生发展的潜在机制仍存在争议。有大量证据表明部分患者的佩吉特病存在遗传基础。有人主张佩吉特病由病毒引起。基于文中回顾的越来越多的证据,另一种涉及该疾病免疫机制的假说也被提出。所呈现的病例显示出非常侵袭性的佩吉特病典型的临床和X线特征。我们推测该病例的极端局部侵袭性是肾移植后长期治疗导致患者并发免疫抑制的继发结果。

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