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伴沙粒体钙化的腱鞘炎:一种独特的与创伤相关的特发性钙化性腱鞘炎亚型,好发于中年女性的四肢末端-23 例报告。

Tenosynovitis With Psammomatous Calcifications: A Distinctive Trauma-Associated Subtype of Idiopathic Calcifying Tenosynovitis With a Predilection for the Distal extremities of Middle-Aged Women-A Report of 23 Cases.

机构信息

Department of Pathology.

Biomedical Center, Charles University, Faculty of Medicine in Pilsen.

出版信息

Am J Surg Pathol. 2019 Feb;43(2):261-267. doi: 10.1097/PAS.0000000000001182.

Abstract

The term "idiopathic calcifying tenosynovitis" (ICT) refers to a clinically and radiologically defined syndrome of pain and tendinous calcifications, most often involving the shoulder joint. A distinctive subset of ICT cases, termed "tenosynovitis with psammomatous calcifications" (TPC), occurs in the distal extremities and shows characteristic morphology, in particular psammomatous calcifications. As only 14 cases have been reported to date, TPC remains poorly recognized by both pathologists and clinicians. Twenty-three well-characterized cases of TPC along with all available radiologic and clinical information, including follow-up, were collected. Cases occurred in 21 females and 1 male (1 patient of unknown sex), aged 16 to 75 years (mean: 41), and almost exclusively involved the fingers and toes, except for one case in the elbow and one in the knee joint. The lesions ranged from 2 to 30 mm in size (mean: 10 mm). Pain was the most common presenting symptom (12/16 patients). A history of trauma or repetitive activity was present in 6 of 15 patients. None of the individuals was known to have disorders in calcium or phosphate metabolism. Radiographic studies showed a nonspecific, calcified mass. Typical morphologic features of TPC were invariably present, with degenerating tendinous tissue containing psammomatous calcifications, surrounded by a variably cellular, CD68/CD163/CD4-positive histiocyte-rich granulomatous host reaction. HUMARA assay in one case showed a polyclonal pattern. Clinical follow-up (19 patients; mean: 5.2 y; range: 1 to 14 y) showed no local recurrences. In this, the largest study of TPC to date, we confirm striking predilection of this distinctive pseudoneoplasm for the fingers and toes of young to middle-aged women. TPC should be rigorously distinguished from other forms of ICT, which typically involve large, proximal joints, and show simply dystrophic calcification involving tendinous tissues, and from tumoral calcinosis, which also involves large joints and often is associated with calcium and/or phosphate abnormalities. TPC appears to be related to trauma and/or repetitive activity and is cured with simple excision.

摘要

“特发性钙化性腱鞘炎”(idiopathic calcifying tenosynovitis,ICT)一词是指一种临床上和影像学上定义明确的疼痛和肌腱钙化综合征,最常涉及肩关节。ICT 的一个独特亚组,称为“伴有砂粒体样钙化的腱鞘炎”(tenosynovitis with psammomatous calcifications,TPC),发生在远端肢体,具有特征性形态,特别是砂粒体样钙化。由于迄今为止仅报道了 14 例病例,TPC 仍然被病理学家和临床医生所忽视。我们收集了 23 例特征明确的 TPC 病例以及所有可用的影像学和临床资料,包括随访。这些病例发生在 21 名女性和 1 名男性(1 名患者性别未知)中,年龄 16 至 75 岁(平均 41 岁),几乎仅累及手指和脚趾,除了 1 例发生在肘部和 1 例发生在膝关节。病变大小为 2 至 30mm(平均 10mm)。疼痛是最常见的首发症状(16 例患者中的 12 例)。15 例患者中有 6 例有创伤或反复活动史。没有一个人患有钙或磷酸盐代谢紊乱。影像学研究显示出一种非特异性的钙化肿块。TPC 的典型形态特征始终存在,包含退化的肌腱组织,含有砂粒体样钙化,被可变细胞、CD68/CD163/CD4 阳性的组织细胞丰富的肉芽肿性宿主反应所包围。一例 HUMARA 检测显示为多克隆模式。临床随访(19 例患者;平均 5.2 年;范围 1 至 14 年)显示无局部复发。在这项迄今为止对 TPC 最大的研究中,我们证实了这种独特假肿瘤对年轻至中年女性手指和脚趾的强烈偏好。TPC 应严格与其他形式的 ICT 区分开来,后者通常涉及大的近端关节,并且仅表现为涉及肌腱组织的退行性钙化,也应与肿瘤性钙化区分开来,后者也涉及大关节,并且常与钙和/或磷酸盐异常有关。TPC 似乎与创伤和/或反复活动有关,通过简单切除即可治愈。

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