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肩周炎的病理学。一种类似掌腱膜挛缩症的疾病。

The pathology of frozen shoulder. A Dupuytren-like disease.

作者信息

Bunker T D, Anthony P P

机构信息

Princess Elizabeth Orthopaedic Hospital, Exeter, England.

出版信息

J Bone Joint Surg Br. 1995 Sep;77(5):677-83.

PMID:7559688
Abstract

Of 935 consecutive patients referred with shoulder pain, 50 fitted the criteria for primary frozen shoulder. Twelve patients who failed to improve after conservative treatment and manipulation had excision of the coracohumeral ligament and the rotator interval of the capsule. The specimens were examined histologically, using special stains for collagen. Immunocytochemistry was performed with monoclonal antibodies against leucocyte common antigen (LCA, CD45) and a macrophage/synovial antigen (PGMI, CD68) to assess the inflammatory component, and vimentin and smooth-muscle actin to evaluate fibroblasts and myofibroblasts. Our histological and immunocytochemical findings show that the pathological process is active fibroblastic proliferation, accompanied by some transformation to a smooth muscle phenotype (myofibroblasts). The fibroblasts lay down collagen which appears as a thick nodular band or fleshy mass. These appearances are very similar to those in Dupuytren's disease of the hand, with no inflammation and no synovial involvement. The contracture acts as a check-rein against external rotation, causing loss of both active and passive movement.

摘要

在935例因肩部疼痛前来就诊的连续患者中,50例符合原发性冻结肩的标准。12例经保守治疗和手法治疗后未见改善的患者接受了喙肱韧带和关节囊旋转间隙切除术。对标本进行组织学检查,使用胶原蛋白特殊染色。采用抗白细胞共同抗原(LCA,CD45)和巨噬细胞/滑膜抗原(PGMI,CD68)的单克隆抗体进行免疫细胞化学检测以评估炎症成分,并用波形蛋白和平滑肌肌动蛋白评估成纤维细胞和肌成纤维细胞。我们的组织学和免疫细胞化学研究结果表明,病理过程为活跃的成纤维细胞增殖,并伴有向平滑肌表型(肌成纤维细胞)的一些转化。成纤维细胞分泌胶原蛋白,形成厚的结节状带或肉质团块。这些表现与手部掌腱膜挛缩症非常相似,无炎症且无滑膜受累。挛缩起到限制外旋的作用,导致主动和被动活动均丧失。

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