原发性多形性乳腺肉瘤--病例报告。

Q4 Dentistry
Daniel Markov, Petar Uchikov, Pavel Timonov, Galabin Markov, Elena Poryazova
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引用次数: 0

摘要

原发性乳腺肉瘤是非常罕见的组织学异质性非上皮性恶性肿瘤。原发性未分化多形性肉瘤是一种罕见的乳腺恶性间质肿瘤。其特点是细胞明显不典型和多形性。文献中常描述一些病程凶险、预后不良的孤立病例。我们报告了一例罕见病例,患者是一名 62 岁女性,左侧乳房长有一个 18 厘米的实体瘤,发病已有 6 个月,最近一个月肿瘤生长迅速。体格检查和乳房 X 光检查显示左侧腋窝无肿大淋巴结。患者接受了全乳房切除术。由于缺乏特异性免疫组化标记,未分化多形性肉瘤的诊断具有挑战性。只有在排除其他类型的软组织肉瘤后才能做出诊断。本报告讨论了所进行的组织病理学和免疫组化研究。我们的病例由于临床表现不典型(无痛、自发性出血)和肿瘤体积较大而与其他诊断相同的病例有所区别。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Primary pleomorphic breast sarcoma - a case report.

Primary mammary sarcomas are very rare, histologically heterogeneous non-epithelial malignant neoplasms. Primary undifferentiated pleomorphic sarcoma is a rare malignant mesenchymal tumor in the breast. It is characterized by marked cellular atypism and pleomorphism. Isolated cases with an aggressive course and poor prognosis have been commonly described in the literature. We present a rare case of a 62-year-old woman with an 18-cm solid tumor of the left breast, 6 months old, which grew rapidly during the last month. Physical examination and mammography revealed no enlarged lymph nodes in the left axilla. A total mastectomy was performed. The diagnosis of undifferentiated pleomorphic sarcoma is challenging due to the lack of specific immunohistochemical markers. It can only be made after excluding other types of soft tissue sarcomas. This report discusses the histopathological and immunohistochemical studies that were conducted. Our case is distinguished from others with the same diagnosis by the atypical clinical presentation, which is painless, and the spontaneous bleeding, as well as the large size of the tumor.

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来源期刊
Folia medica
Folia medica Medicine-Medicine (all)
CiteScore
1.00
自引率
0.00%
发文量
121
审稿时长
5 weeks
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