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肢端外生性和指(趾)内生性血管球瘤的临床和病理特征:一项回顾性对比研究。

Clinical and pathological characteristics of extradigital and digital glomus tumours: a retrospective comparative study.

机构信息

Department of Dermatology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea.

出版信息

J Eur Acad Dermatol Venereol. 2011 Dec;25(12):1392-7. doi: 10.1111/j.1468-3083.2011.03979.x. Epub 2011 Mar 4.

Abstract

BACKGROUND

Most glomus tumours are located in the digits, especially in subungual areas. Less is known, however, about the clinical characteristics of extradigital glomus tumours.

OBJECTIVES

The aim of this study was to characterize extradigital glomus tumours and compare their clinical, pathological and immunohistochemical characteristics with those of digital glomus tumours.

METHODS

We retrospectively reviewed the charts of 110 patients with digital and 42 patients with extradigital glomus tumours, treated at a single centre from 1991 to 2010. We also investigated the immunohistochemical expression of substance P and TRPV1 in the biopsy specimens from patients with digital (n = 5) and extradigital (n = 5) glomus tumours.

RESULTS

Compared with patients with digital glomus tumours, patients with extradigital tumours were significantly older (P = 0.009) and showed a significantly greater male predominance (P < 0.001), lower incidence rates of pain (P = 0.019), cold intolerance (P < 0.001) and a higher frequency of the glomangioma subtype (P < 0.001). Extradigital glomus tumours were located most frequently on the upper extremities (n = 25). The most common clinical presentations were solitary purplish papules (n = 10). Only 20% of extradigital glomus tumours were diagnosed correctly by the initial physician. Of 38 evaluable patients, 34 (89.5%) were successfully treated with simple excision without recurrence. Substance P and TRPV1 were expressed moderately to strongly in glomus cells, but there were no differences in their expression between patients with digital and extradigital glomus tumours.

CONCLUSION

Extradigital glomus tumours do not have specific clinical features such as pain, leading to frequent misdiagnosis. To prevent delay in diagnosis or misdiagnosis, it is important to increase awareness of these tumours.

摘要

背景

大多数血管球瘤位于手指,特别是甲下区域。然而,关于指外血管球瘤的临床特征知之甚少。

目的

本研究旨在描述指外血管球瘤的临床特征,并比较其与指部血管球瘤的临床、病理和免疫组化特征。

方法

我们回顾性分析了 1991 年至 2010 年在一家中心治疗的 110 例指部和 42 例指外血管球瘤患者的病历。我们还研究了 5 例指部和 5 例指外血管球瘤患者活检标本中 P 物质和 TRPV1 的免疫组化表达。

结果

与指部血管球瘤患者相比,指外血管球瘤患者年龄明显较大(P = 0.009),男性优势明显(P < 0.001),疼痛发生率较低(P = 0.019),冷不耐受(P < 0.001)和血管球瘤亚型发生率较高(P < 0.001)。指外血管球瘤最常发生在上肢(n = 25)。最常见的临床表现是单发紫色丘疹(n = 10)。只有 20%的指外血管球瘤被初始医生正确诊断。在 38 例可评估患者中,34 例(89.5%)患者经单纯切除后成功治疗,无复发。P 物质和 TRPV1 在血管球细胞中表达中等至强阳性,但在指部和指外血管球瘤患者中表达无差异。

结论

指外血管球瘤没有疼痛等特定的临床特征,导致频繁误诊。为了防止诊断延误或误诊,提高对这些肿瘤的认识非常重要。

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