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足底的黏液软骨样化生:一种具有特征性的假性肿瘤病变,类似于项韧带纤维软骨假瘤和马数字软垫。

Myxochondroid metaplasia of the plantar foot: a distinctive pseudoneoplastic lesion resembling nuchal fibrocartilaginous pseudotumor and the equine digital cushion.

机构信息

Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.

出版信息

Mod Pathol. 2013 Dec;26(12):1561-7. doi: 10.1038/modpathol.2013.116. Epub 2013 Jun 14.

DOI:10.1038/modpathol.2013.116
PMID:23765248
Abstract

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.

摘要

软组织软骨肿瘤并不常见,良性的软部软骨瘤远多于罕见的软组织软骨肉瘤。在过去的几年中,我们在会诊中观察到一种独特的、良性的足底软组织软骨样病变,与软部软骨瘤在许多方面不同。在此,我们报告我们对此独特病变的经验。对我们软组织会诊和机构外科病理档案中所有足部病例进行回顾性分析,确定了 9 例类似病例,这些病例大多以前被编码为“纤维连接组织伴软骨化生”。由于担心是肿瘤性病变,特别是软部软骨瘤或指部纤维-骨假性肿瘤,有 6 例病例提交会诊。这些患者为 4 名年轻男性(年龄 8-16 岁,平均 11.5 岁)和 5 名老年患者,包括 4 名女性和 1 名男性(年龄 34-78 岁,平均 56.4 岁)。所有病例均发生在足底皮下软组织,包括 4 例局限于趾部,表现为非特异性、不同程度疼痛的肿块。6 例中有 6 例可获得影像学研究,均未见骨受累证据。组织学上,病变的特征是在具有明显基质嗜碱性和软骨样外观的纤维粘液样背景中,部分界限清楚的、细胞数量不等的纤维母细胞增生。偶尔可见小灶性真性软骨化生伴陷窝形成。在 3 例病例中,用 S100 和 ERG 蛋白的免疫组化证实了软骨分化。瘤内囊性变很常见,周围结缔组织也有多种其他反应性改变。缺乏软部软骨瘤和/或指部纤维-骨假性肿瘤的典型形态特征。7 例患者(2-115 个月,中位数 38 个月)的临床随访显示所有患者均无疾病复发。我们已经确定了足部一种形态独特的病变,它似乎代表一种反应性、化生过程,可能继发于慢性机械性应激。足底粘液软骨化生的形态特征与颈项纤维软骨假瘤和马的数字垫相似,进一步提示其具有反应性/修复性病因。认识到该病变的独特特征应能使其与足部其他肿瘤性和假性(骨)软骨性病变轻易区分开来。

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Myxochondroid metaplasia of the plantar foot: a distinctive pseudoneoplastic lesion resembling nuchal fibrocartilaginous pseudotumor and the equine digital cushion.足底的黏液软骨样化生:一种具有特征性的假性肿瘤病变,类似于项韧带纤维软骨假瘤和马数字软垫。
Mod Pathol. 2013 Dec;26(12):1561-7. doi: 10.1038/modpathol.2013.116. Epub 2013 Jun 14.
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