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佩吉特病的溶骨型。鉴别诊断与发病机制。

Osteolytic form of Paget's disease. Differential diagnosis and pathogenesis.

作者信息

Anderson J T, Dehner L P

出版信息

J Bone Joint Surg Am. 1976 Oct;58(7):994-1000.

PMID:977632
Abstract

Of fourteen patients with Paget's disease for whom adequate roentgenograms and pathological material were available, six had lesions showing significant or predominant osteolysis. Based on a study of these six patients and a review of the literature, the following mechanisms were identified as causes of the so-called osteolytic type of the disease: (1) an "early" destructive Paget's lesion; (2) "advanced" Paget's disease with secondary degenerative changes; (3) "seeding" of an independent osteolytic lesion, particularly tumor in pre-existing Paget's disease; (4) sarcomatous transformation; and (5) immobilization after fracture. An osteolytic lesion in a patient without other bone disease may be due to Paget's disease, while an associated lytic lesion may be the result of a variety of conditions. Accurate pathological diagnosis is essential.

摘要

在14例有足够X线片和病理材料的佩吉特病患者中,6例有显示明显或主要骨质溶解的病变。基于对这6例患者的研究及文献回顾,以下机制被确定为所谓溶骨型该疾病的病因:(1)“早期”破坏性佩吉特病变;(2)伴有继发性退行性改变的“晚期”佩吉特病;(3)独立溶骨病变的“播散”,特别是在已有佩吉特病基础上的肿瘤;(4)肉瘤变;(5)骨折后制动。无其他骨病患者的溶骨病变可能归因于佩吉特病,而相关的溶骨性病变可能是多种情况的结果。准确的病理诊断至关重要。

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