乳房原发性滑膜肉瘤最初与隆突性皮肤纤维肉瘤相似:1例报告。

IF 1.7 Q4 ONCOLOGY
Ines Mkhinini, Hammadi Jawaher, Samar Knaz, Nour Rouis, Chayma Selmi, Amira Ounissi, Rania Boukadida, Yosra Fejji, Salwa Mejri, Ridha Fatnassi
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引用次数: 0

摘要

原发性乳腺滑膜肉瘤是一种极为罕见的恶性肿瘤,占乳腺肿瘤的不到1%。它的临床表现可以模仿其他梭形细胞肿瘤,包括皮肤纤维肉瘤隆突(DFSP),使诊断具有挑战性。我们报告一例60岁的绝经后妇女,在左乳房上外侧象限出现一个坚固的,可移动的10厘米肿块,影像学分类为乳房ımaging报告和数据系统4。由于CD34阳性,核心针活检最初提示为DFSP。单纯的乳房切除术显示高度细胞化,纺锤状细胞肿瘤排列在束状,形成典型的螺旋状模式。免疫组化显示CD34阴性,分裂1转导样增强子阳性,b细胞淋巴瘤2阳性,局灶上皮膜抗原阳性。分子分析证实SYT-SSX1融合,确立了单相滑膜肉瘤的诊断。手术切缘阴性,一年随访显示患者无疾病。本病例强调了免疫组织化学和分子检测对准确诊断和适当治疗的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Primary Synovial Sarcoma of the Breast Initially Mimicking Dermatofibrosarcoma Protuberans: A Case Report.

Primary synovial sarcoma of the breast is an extremely rare malignancy, representing less than 1% of breast tumors. Its clinical presentation can mimic other spindle cell neoplasms, including dermatofibrosarcoma protuberans (DFSP), making diagnosis challenging. We report the case of a 60-year-old postmenopausal woman presenting with a firm, mobile 10 cm mass in the upper outer quadrant of the left breast, classified on imaging as breast ımaging reporting and data System 4. A core needle biopsy initially suggested DFSP because of strong CD34 positivity. A simple mastectomy revealed a highly cellular, spindle-cell tumor arranged in fascicles, forming a characteristic whorled pattern. Immunohistochemistry showed CD34 negativity, transducin-like enhancer of split 1 positivity, B-cell lymphoma 2 positivity, and focal epithelial membrane antigen positivity. Molecular analysis confirmed SYT-SSX1 fusion, establishing the diagnosis of monophasic synovial sarcoma. Surgical margins were negative, and one-year follow-up showed that the patient remained disease-free. This case highlights the importance of immunohistochemistry and molecular testing for accurate diagnosis and appropriate management.

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