Suppr超能文献

乳腺隆突性皮肤纤维肉瘤

Dermatofibrosarcoma protuberans of the breast.

作者信息

Lin Jong-Yueh, Sheen-Chen Shyr-Ming, Hsu Wayne, Huang Chao-Cheng, Ko Sheung-Fat, Eng Hock-Liew

机构信息

Department of Surgery, Chang Gung Memorial Hospital, Kaohsiung Medical Center College of Medicine, Chang Gung University, Niao-Sung Hsiang, Kaohsiung Hsien, Taiwan.

出版信息

Tumori. 2008 Nov-Dec;94(6):861-3. doi: 10.1177/030089160809400616.

Abstract

BACKGROUND

Dermatofibrosarcoma protuberans is an uncommon, locally aggressive but rarely metastasizing tumor of the deep dermis and subcutaneous tissue. It may occur at almost any site but is most common in the trunk and extremities. Dermatofibrosarcoma protuberans of the breast has been rarely reported.

CASE PRESENTATION

A 49-year-old woman without a significant medical history presented with a right breast mass that had been present for more than 10 years. Recently, progressive enlargement of the mass was noted. Physical examination showed a firm, well-defined, non-tender, mobile, erythematous 2 x 2 cm mass in the upper outer part of the right breast. Breast sonography showed a 2.3 x 1 cm slightly heteroechoic nodule with uneven anterior contours located in the dermal layer, highly suggestive of a dermal lesion. Wide excision of the mass was performed. Microscopically, the hypercellular tumor was composed of relatively monomorphic spindle cells forming a storiform pattern around the sweat glands of the deep dermis and the subcutaneous fat vacuoles. The tumor cells showed strong immunoreactivity for CD34. The final histological diagnosis was dermatofibrosarcoma protuberans.

CONCLUSIONS

Dermatofibrosarcoma protuberans of the breast, though uncommon, does exist. With the awareness of this entity can a prompt diagnosis be made and the disease be properly managed.

摘要

背景

隆突性皮肤纤维肉瘤是一种罕见的、局部侵袭性但很少发生转移的真皮深层和皮下组织肿瘤。它几乎可发生于任何部位,但最常见于躯干和四肢。乳腺隆突性皮肤纤维肉瘤鲜有报道。

病例介绍

一名49岁无重大病史的女性,右乳肿物已存在10余年。近期发现肿物逐渐增大。体格检查显示右乳外上象限有一个质地硬、边界清晰、无压痛、可活动的2×2 cm红斑性肿物。乳腺超声显示位于真皮层的一个2.3×1 cm稍具异质性回声的结节,前缘轮廓不平整,高度提示为真皮病变。对肿物进行了广泛切除。显微镜下,细胞丰富的肿瘤由相对单一形态的梭形细胞组成,围绕真皮深层的汗腺和皮下脂肪空泡形成席纹状结构。肿瘤细胞对CD34呈强免疫反应性。最终组织学诊断为隆突性皮肤纤维肉瘤。

结论

乳腺隆突性皮肤纤维肉瘤虽不常见,但确实存在。认识到这一实体才能做出及时诊断并对疾病进行妥善处理。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验