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系统性特发性纤维化和系统性韦格纳-克里斯蒂安病。

Systemic idiopathic fibrosis and systemic Weber-Christian disease.

作者信息

Mitchinson M J

出版信息

J Clin Pathol. 1965 Sep;18(5):645-9. doi: 10.1136/jcp.18.5.645.

Abstract

Idiopathic retroperitoneal fibrosis is represented as one of the manifestations of a widespread disease, systemic idiopathic fibrosis. Some evidence is presented which suggests its origin as an inflammatory disease of adipose tissue. Although relatively rare, the idiopathic diseases of adipose tissue and its blood vessels are worthy of closer study.

摘要

特发性腹膜后纤维化是一种广泛存在的疾病——系统性特发性纤维化的表现之一。本文提供了一些证据,表明其起源为脂肪组织的炎症性疾病。尽管相对罕见,但脂肪组织及其血管的特发性疾病值得深入研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d21c/473033/b4a0be96d743/jclinpath00358-0069-a.jpg

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