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细胞性数字纤维瘤:一种独特的CD34阳性病变,可能酷似隆突性皮肤纤维肉瘤。

Cellular digital fibromas: distinctive CD34-positive lesions that may mimic dermatofibrosarcoma protuberans.

作者信息

McNiff Jennifer M, Subtil Antonio, Cowper Shawn E, Lazova Rossitza, Glusac Earl J

机构信息

Departments of Dermatology and Pathology, Yale University School of Medicine, New Haven, CT, USA.

出版信息

J Cutan Pathol. 2005 Jul;32(6):413-8. doi: 10.1111/j.0303-6987.2005.00358.x.

Abstract

BACKGROUND

Digital fibromas are common benign acral tumors typically reported as angiofibromas (AFs) or acquired digital fibrokeratomas (ADFs). Cellular variants are not well recognized.

METHODS

We collected 14 acral fibrocytic lesions showing a spindle cell morphology from our files, and evaluated CD34, Factor XIIIa, epithelial membrane antigen (EMA), and S100 protein staining of these lesions. We compared the histologic and immunohistochemical features of these cellular fibromas with five digital AFs, five ADFs, and five digital dermatofibromas.

RESULTS

The 14 cellular digital fibromas showed intersecting fascicles of thin delicate bland spindle cells in the superficial reticular dermis with a fibrotic-to-slight myxoid stroma. The spindle cells in all cases stained strongly for CD34, and only scattered stromal cells stained for Factor XIIIa. Five tested cases were negative for EMA and S100 protein. The digital AFs, fibrokeratomas, and dermatofibromas stained predominately for Factor XIIIa, with no or minimal staining for CD34.

CONCLUSIONS

These findings suggest that a subset of digital fibromas is characterized by a dense cellular proliferation of CD34-positive spindle cells. Awareness of this variant of digital fibroma and its staining pattern is critical in preventing misdiagnosis as dermatofibrosarcoma protuberans, particularly in superficial biopsies.

摘要

背景

指部纤维瘤是常见的良性肢端肿瘤,通常被报道为血管纤维瘤(AFs)或获得性指部纤维角化瘤(ADFs)。细胞变异型尚未得到充分认识。

方法

我们从存档病例中收集了14例显示梭形细胞形态的肢端纤维细胞性病变,并评估了这些病变的CD34、凝血因子XIIIa、上皮膜抗原(EMA)和S100蛋白染色情况。我们将这些细胞性纤维瘤的组织学和免疫组化特征与5例指部AFs、5例ADFs和5例指部皮肤纤维瘤进行了比较。

结果

14例细胞性指部纤维瘤在浅表网状真皮层显示出纤细、温和的梭形细胞相互交织的束状结构,伴有纤维化至轻度黏液样基质。所有病例中的梭形细胞CD34染色均呈强阳性,只有散在的基质细胞凝血因子XIIIa染色阳性。5例检测病例EMA和S100蛋白染色均为阴性。指部AFs、纤维角化瘤和皮肤纤维瘤主要为凝血因子XIIIa染色阳性,CD34染色无或极少。

结论

这些发现表明,一部分指部纤维瘤的特征是CD34阳性梭形细胞的密集细胞增殖。认识到这种指部纤维瘤变异型及其染色模式对于防止误诊为隆突性皮肤纤维肉瘤至关重要,尤其是在浅表活检中。

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