Umanah Ivy N, Okpongette Akpan S
Departments of Pathology and.
Rare Tumors. 2009 Dec 28;1(2):e50. doi: 10.4081/rt.2009.e50.
We report the case of a 21-year-old Nigerian woman who presented to us with features of intracystic papillary carcinoma, a rare form of breast cancer usually seen in postmenopausal women in their sixth to eighth decades of life. To the best of our knowledge, there has been only one other case report of this lesion occurring in women in their second decade of life.Physical examination showed a well-defined mass, 54 mm in diameter, in the upper proximal quadrant of the right breast close to the areola, histologically composed of monotypic epithelial cells disposed in solid, cystic, and papillary patterns. A diagnosis of intracystic papillary carcinoma was made because of the presence of intracystic arborization of the fibrovascular stroma, a monotonous cell population, the presence of mitoses, and the lack of myoepithelial cells determined by immunohistochemistry using calponin and p63 stains. Estrogen receptor status was positive while progesterone status and HER-2-neu receptor status were negative.The patient has survived for 12 months without any sign of recurrence after the last surgical resection of the tumor.
我们报告了一例21岁尼日利亚女性的病例,她表现出囊内乳头状癌的特征,这是一种罕见的乳腺癌形式,通常见于60至80岁的绝经后女性。据我们所知,仅有另一例关于该病变发生在20岁女性中的病例报告。体格检查发现右乳房靠近乳晕的上象限有一个边界清晰的肿块,直径54毫米,组织学上由呈实性、囊性和乳头状排列的单型上皮细胞组成。由于纤维血管间质存在囊内分支、细胞群体单一、有丝分裂存在以及使用钙调蛋白和p63染色通过免疫组织化学确定缺乏肌上皮细胞,故诊断为囊内乳头状癌。雌激素受体状态为阳性,而孕激素状态和HER-2-neu受体状态为阴性。该患者在最后一次肿瘤手术切除后已存活12个月,无任何复发迹象。