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首页> 外文期刊>Modern Pathology >Myxochondroid metaplasia of the plantar foot: a distinctive pseudoneoplastic lesion resembling nuchal fibrocartilaginous pseudotumor and the equine digital cushion
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Myxochondroid metaplasia of the plantar foot: a distinctive pseudoneoplastic lesion resembling nuchal fibrocartilaginous pseudotumor and the equine digital cushion

机译:足底脚的线粒体化生:一种独特的假瘤性病变,类似于颈部纤维oc关节假瘤和马指垫

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Cartilaginous tumors of soft tissue are uncommon, with benign chondromas of soft parts greatly outnumbering rare soft-tissue chondrosarcomas. Over the past several years, we have seen in consultation a distinctive, benign-appearing chondroid soft-tissue lesion of the plantar foot that differs in a number of respects from chondroma of soft parts. Herein we report our experience with this distinctive lesion. A retrospective review of all cases from the foot in our soft-tissue consultation and institutional surgical pathology archives identified 9 similar cases, most often previously coded as ‘fibroconnective tissue with chondroid metaplasia’. Six cases were submitted in consultation due to concern for a neoplastic process, in particular chondroma of soft parts or fibro-osseous pseudotumor of the digits. The patients were 4 young males (age range 8–16 years, mean 11.5 years) and 5 older patients, including 4 women and 1 man (age range 34–78 years, mean 56.4 years). All cases occurred in the subcutaneous plantar soft tissues of the feet, including four cases confined to the toes, and presented as non-specific, variably painful masses. Radiographic studies, available in six cases, did not show any evidence of bone involvement. Histologically, the lesions were characterized by a partially circumscribed, variably cellular proliferation of bland fibroblastic cells in a fibromyxoid background in areas showing distinct stromal basophilia and a chondroid appearance. Small foci of true cartilaginous metaplasia with lacuna formation were occasionally seen. Cartilaginous differentiation was confirmed in three cases with immunohistochemistry for S100 and ERG proteins. Intralesional cystic change was common, as were a variety of other reactive-appearing changes in the surrounding connective tissue. Characteristic morphological features of chondroma of soft parts and/or fibro-osseous pseudotumor of the digits were absent. Clinical follow-up (7 patients, 2–115 months, median 38 months) showed all patients to be without recurrent disease. We have identified a morphologically distinctive lesion of the foot that appears to represent a reactive, metaplastic process, presumably secondary to chronic mechanical stress. The morphological features of myxochondroid metaplasia of the plantar foot are reminiscent of those of nuchal fibrocartilaginous pseudotumor and the equine digital cushion, further suggesting a reactive/reparative etiology. Awareness of the unique features of this lesion should allow its ready distinction from other neoplastic and pseudoneoplastic (osteo) cartilaginous lesions of the feet.
机译:软组织的软骨肿瘤并不常见,软组织的良性软骨瘤大大超过罕见的软组织软骨肉瘤。在过去的几年中,我们在会诊中发现了一种独特的,良性的足底软骨样软组织病变,该病变在很多方面与软性部分软骨瘤有所不同。在这里,我们报告我们对这种独特病变的经验。在我们的软组织咨询和机构手术病理学档案中,对足部所有病例进行了回顾性研究,发现9例相似的病例,以前通常被编码为“软骨样化生的纤维结缔组织”。由于担心肿瘤形成过程,特别是手指软组织软骨瘤或手指纤维性骨假瘤,提出了六例咨询。患者为4名男性青年(年龄8-16岁,平均11.5岁)和5名老年患者,其中4名女性和1名男性(年龄34-78岁,平均56.4岁)。所有病例均发生在脚的皮下足底软组织中,其中四例局限于脚趾,并表现为非特异性的可变疼痛性肿块。在六例病例中进行的放射学研究未显示任何骨受累的证据。从组织学的角度来看,病变的特征是在纤维粘胶样背景下,在区域内表现出明显的间质嗜碱性和软骨样变的区域中,温和的成纤维细胞发生了部分限制的可变细胞增殖。偶尔见到真正的软骨化生伴腔形成的小灶。在三例S100和ERG蛋白免疫组织化学检查中证实了软骨分化。肠内囊变是常见的,周围结缔组织中还有许多其他反应性变化。缺乏手指软组织软骨瘤和/或手指骨性假瘤的形态学特征。临床随访(7例,2–115个月,中位38个月)显示所有患者均未复发。我们已经确定了足部形态上独特的病变,似乎代表了反应性的,化生过程,大概是继发于慢性机械应力的。足底线粒体化生的形态特征使人想起了颈纤维oc关节假瘤和马指垫,进一步提示了反应性/修复性病因。意识到该病变的独特特征,应使其与足部其他赘生性和假赘生性(骨)软骨性病变区分开来。

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