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皮肤脂肪瘤性神经纤维瘤:特征与发生率

Cutaneous lipomatous neurofibroma: characterization and frequency.

作者信息

Val-Bernal J Fernando, González-Vela M Carmen

机构信息

Department of Anatomical Pathology, Marqués de Valdecilla University Hospital, University of Cantabria, Santander, Spain.

出版信息

J Cutan Pathol. 2005 Apr;32(4):274-9. doi: 10.1111/j.0303-6987.2005.00311.x.

Abstract

BACKGROUND

There are numerous variants of cutaneous neurofibroma reflecting its manner of growth and histologic composition. Lipomatous neurofibroma is the latest described variant with only eight cases reported.

METHODS

A systematic study based on 320 consecutive specimens diagnosed of cutaneous neurofibroma was carried out. Conventional microscopy, immunohistochemistry, and statistical methods were used to determine the presence of fat cells, their amount, distribution, and frequency.

RESULTS

Intratumoral fat was observed in 22 (6.9%) neurofibromas. All these were dermal neurofibromas. Intraneoplastic fat was divided into two groups: focal and diffuse (regularly interspersed). Eighteen tumors (5.6%) presented adipocytes focally intermingled with the spindle cells. There were four (1.3%) neurofibromas showing spindle cell proliferation with regularly scattered adipocytes. Lipomatous neurofibroma was more frequent located on head and neck than non-lipomatous neurofibroma ( p = 0.04). Neurofibromas without mature adipocytes were more frequently immunoreactive for CD34 compared with tumors showing intratumoral fat ( p = 0.02).

CONCLUSIONS

We suggest that both metaplasia and aberrant adipose differentiation from multipotential cells may result in lipomatous neurofibroma. Focal presence of adipose cells may be attributable to metaplasia as the pathogenic mechanism. The fatty tissue being intrinsic to the tumor structure in its diffuse form, the lesion represents a distinctive tumor of the peripheral nerve sheath.

摘要

背景

皮肤神经纤维瘤有多种变体,反映了其生长方式和组织学组成。脂肪瘤样神经纤维瘤是最新描述的变体,仅报道了8例。

方法

对320例连续诊断为皮肤神经纤维瘤的标本进行了系统研究。采用传统显微镜检查、免疫组织化学和统计学方法来确定脂肪细胞的存在、数量、分布和频率。

结果

在22例(6.9%)神经纤维瘤中观察到瘤内脂肪。所有这些均为真皮神经纤维瘤。瘤内脂肪分为两组:局灶性和弥漫性(规则散在)。18例肿瘤(5.6%)呈现脂肪细胞与梭形细胞局灶性混合。有4例(1.3%)神经纤维瘤显示梭形细胞增生并伴有规则散在的脂肪细胞。脂肪瘤样神经纤维瘤比非脂肪瘤样神经纤维瘤更常见于头颈部(p = 0.04)。与显示瘤内脂肪的肿瘤相比,无成熟脂肪细胞的神经纤维瘤对CD34的免疫反应性更高(p = 0.02)。

结论

我们认为化生以及多能细胞的异常脂肪分化都可能导致脂肪瘤样神经纤维瘤。脂肪细胞的局灶性存在可能归因于化生作为致病机制。脂肪组织以弥漫形式存在于肿瘤结构中,该病变代表一种独特的周围神经鞘肿瘤。

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