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[苏戴克氏病]

[Sudeck disease].

作者信息

Enderle A, Gregl A

机构信息

Orthopädischen Universitätsklinik, Universitätsklinik Göttingen.

出版信息

Z Lymphol. 1990 Dec;14(2):68-75.

PMID:1708182
Abstract

In 1900, the Hamburg surgeon P.H.M. Sudeck was the first to describe the clinical and radiological symptomatology of the disorder to which he later lent his name. He devoted his scientific career to this disorder, "acute inflammatory atrophy" of bone and soft-tissue as he called it. He elaborated the histology of the disorder with his students and advocated the pathogenic peripheral humoral theory. In later years seven further attempts to explain the pathogenesis were published. The present paper notes that this disorder, which can be divided into three distinct stages, is diagnosed mainly on the basis of clinical factors, above all in the early stage, and that x-rays in the early stages are difficult to differentiate from those of immobilisation osteoporosis since both disorders can manifest as patchy rare fraction and fibrous osteolysis in subchondral bone and old growth plates. Moreover, the author also notes that 10% of all Sudeck cases are not preceded by trauma; these must be understood as spontaneous Sudeck or as Sudeck after distant disturbances. A few sources also refer to Sudeck's dystrophy in the presence of lymphatic congestion. Another, special form of Sudeck's atrophy, is the shoulder-hand syndrome which, however, cannot always be differentiated precisely from rheumatic disorders or dystrophic contractures.

摘要

1900年,汉堡外科医生P.H.M. 苏戴克首次描述了这种后来以他的名字命名的疾病的临床和放射学症状。他将自己的科学事业奉献给了这种疾病,即他所称的骨与软组织的“急性炎症性萎缩”。他与学生们详细阐述了该疾病的组织学,并倡导致病性外周体液理论。在随后的几年里,又发表了另外七种关于发病机制的解释。本文指出,这种可分为三个不同阶段的疾病主要根据临床因素进行诊断,尤其是在早期阶段,而且早期的X射线很难与固定性骨质疏松症的X射线区分开来,因为这两种疾病都可能表现为软骨下骨和陈旧生长板中的斑片状稀疏区和纤维性骨质溶解。此外,作者还指出,所有苏戴克病例中有10%在发病前没有受过创伤;这些病例必须被理解为自发性苏戴克病或远距离干扰后的苏戴克病。一些资料还提到了存在淋巴充血时的苏戴克营养不良症。苏戴克萎缩的另一种特殊形式是肩手综合征,然而,它并不总是能与风湿性疾病或营养不良性挛缩精确区分开来。

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