Warner Wayne A, Sookdeo Vandana Devika, Fortuné Maurice, Akhilesh Meenakshi, Rao Adidam Venkata Chalapathi, Mohammed Wayne, Ramkissoon Cassandra, Harnanan Dave, Pran Lemuel, Maharaj Ravi
Division of Oncology, Siteman Cancer Center, Washington University School of Medicine, St. Louis, MO 63110, USA; Department of Cell Biology and Physiology, Washington University School of Medicine, St. Louis, MO 63110, USA.
Department of Clinical Surgical Sciences, University of the West Indies, Eric Williams Medical Sciences Complex,Champ Fleurs, Trinidad and Tobago.
Int J Surg Case Rep. 2017;41:259-264. doi: 10.1016/j.ijscr.2017.09.021. Epub 2017 Oct 4.
Phyllodes tumors (PTs) of the breast are extremely rare accounting for less than 1% of all breast tumors globally. Case records at the Trinidad and Tobago Cancer Registry show that only 0.003% of the reported breast cancer cases between 1995 and 2009 were PTs.
We report a 45-year-old woman who presented with swelling of the left breast. Ultrasound, mammogram and computed tomography imaging confirmed the presence of a mass in the right upper inner quadrant of the left breast. A biopsy revealed features supportive of a benign phyllodes tumor. A wide local excision was performed with the removal of a 19×11×10cm mass. Histopathological analysis revealed features consistent with malignant phyllodes tumor. A complete mastectomy of the left breast was subsequently performed. Follow up over a 5-year period did not reveal any evidence of local recurrence or residual disease. To the best of our knowledge, this is the first case report of a malignant PT from the Caribbean and Latin America.
Phyllodes tumors are classified as benign, borderline, or malignant based on histologic features including presence of a clear margin, cellularity, stromal overgrowth, tumor necrosis and mitotic index. The clinical challenge is to assess the risk of local tumor and metastatic recurrence in the context of fluid classifications.
Our case management approach shows that for patients with malignant PT, a thorough preoperative workup regimen followed by appropriate surgical intervention can result in a desirable prognosis.
乳腺叶状肿瘤(PTs)极为罕见,在全球所有乳腺肿瘤中占比不到1%。特立尼达和多巴哥癌症登记处的病例记录显示,在1995年至2009年报告的乳腺癌病例中,只有0.003%是叶状肿瘤。
我们报告一名45岁女性,其左乳出现肿胀。超声、乳房X线摄影和计算机断层扫描成像证实左乳右上内象限有一肿块。活检显示有支持良性叶状肿瘤的特征。进行了广泛局部切除,切除了一个19×11×10cm的肿块。组织病理学分析显示与恶性叶状肿瘤一致的特征。随后对左乳进行了全乳切除术。5年的随访未发现任何局部复发或残留疾病的证据。据我们所知,这是加勒比和拉丁美洲首例恶性叶状肿瘤的病例报告。
叶状肿瘤根据组织学特征分为良性、交界性或恶性,这些特征包括切缘清晰、细胞密度、间质过度生长、肿瘤坏死和有丝分裂指数。临床挑战在于在不确定分类的情况下评估局部肿瘤和转移复发的风险。
我们的病例管理方法表明,对于恶性叶状肿瘤患者,术前进行全面的检查方案,随后进行适当的手术干预,可获得理想的预后。