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Histopathology of tenosynovium in trigger fingers

机译:触发手指中腱鞘的组织病理学

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Stenosing flexor tenosynovitis, trigger finger, is a common clinical disorder causing painful locking or contracture of the involved digits, and most instances are idiopathic. This problem is generally caused by a size mismatch between the swollen flexor tendon and the thickened first annular pulley. Although hypertrophic pulleys have been histologically and ultrasonographically detected, little is known about the histopathology of the tenosynovium covering the tendons of trigger fingers. We identified chondrocytoid cells that produced hyaluronic acid in 23 (61%) fingers and hypocellular collagen matrix in 32 (84%) fingers around the tenosynovium among 38 specimens of tenosynovium from patients with trigger fingers. These chondrocytoid cells expressed the synovial B cell marker CD44, but not the chondrocyte marker S-100 protein. The incidence of these findings was much higher than that of conventional findings of synovitis, such as inflammatory infiltrate (37%), increased vascularity (37%), hyperplasia of synovial lining cells (21%), or fibrin exudation (5%). We discovered the following distinctive histopathological features of trigger finger: hyaluronic acid-producing chondrocytoid cells originated from fibroblastic synovial B cells, and a hypocellular collagen matrix surrounding the tenosynovium. Thus, an edematous extracellular matrix with active hyaluronic acid synthesis might increase pressure under the pulley and contribute to the progression of stenosis.
机译:狭窄性屈肌腱鞘炎(触发手指)是一种常见的临床疾病,会引起相关指的疼痛锁定或挛缩,大多数情况是特发性的。这个问题通常是由于屈肌腱和增厚的第一环形皮带轮之间的尺寸不匹配引起的。尽管肥大性滑轮在组织学和超声检查中已被发现,但关于腱鞘覆盖扳机指腱的组织病理学知之甚少。我们在38例腱鞘炎患者样本中,在腱鞘周围发现了23个(61%)手指中的透明质酸软骨细胞和32个手指(84%)中的透明质酸胶原基质。这些软骨细胞表达滑膜B细胞标记CD44,但不表达软骨细胞标记S-100蛋白。这些发现的发生率比滑膜炎的常规发现要高得多,例如炎性浸润(37%),血管增加(37%),滑膜衬里细胞增生(21%)或纤维蛋白渗出(5%)。我们发现了扳机指的以下独特组织病理学特征:透明质酸产生的软骨细胞起源于成纤维滑膜B细胞,以及腱鞘周围的低细胞胶原基质。因此,具有活跃的透明质酸合成功能的水肿细胞外基质可能会增加滑轮下的压力并有助于狭窄的发展。

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