Reikie Brian A, Yilmaz Asli, Medlicott Shaun, Trpkov Kiril
*Department of Medicine, University of Calgary †Department of Pathology and Laboratory Medicine, University of Calgary and Calgary Laboratory Services, Calgary, AB, Canada.
Adv Anat Pathol. 2015 Mar;22(2):113-20. doi: 10.1097/PAP.0000000000000057.
In contrast to the common tumors of the prostate, seminal vesicle demonstrates low potential for neoplastic proliferation. Of the rare primary seminal vesicle tumors, adenocarcinoma is the most common, but there are also rare seminal vesicle neoplasms which demonstrate epithelial and stromal components. These neoplasms have been described in the literature under various names, including "epithelial-stromal tumor," "cystic epithelial-stromal tumor," "cystadenoma," "cystomyoma," "mesenchymoma," "Müllerian adenosarcoma-like tumor," "phyllodes tumor," and "cystosarcoma phyllodes." The spectrum of reported mixed epithelial-stromal tumors (MEST) of seminal vesicle encompasses low, intermediate and high-grade tumors, but the precise distinction and nomenclature for these tumors remain unsettled. We propose a common nomenclature for these tumors, based on the review of published cases and 2 index cases from our practice, which represent the low-grade category. The first patient was 46 years old and presented with seminal vesicle neoplasm detected on routine rectal examination. The neoplasm measured 4 cm in greatest dimension, and completely replaced the left seminal vesicle. The tumor was circumscribed and consisted of multiple cysts separated by spindle-cell stroma. The second patient was a 60-year-old man, who had an incidental seminal vesicle neoplasm, which was discovered when he underwent a radical prostatectomy for a prostatic adenocarcinoma, (Gleason score 3+4, stage 3a). Both neoplasms contained hypercellular stroma, which was composed of uniform spindle cells, arranged in fascicles and interspersed between the glands. Both tumors lacked worrisome morphology, such as infiltrative borders, cell atypia, increased mitotic activity, hemorrhage, and necrosis. The stromal cells were reactive for estrogen and progesterone receptors, and desmin. The cysts and dilated glands were lined by epithelial cells, which were positive for cytokeratin 7 and were negative for prostate-specific antigen and prostate-specific acid phosphatase. The first patient underwent prostatectomy and was alive and without evidence of disease recurrence or progression after 11 years of follow-up. Similarly, the second patient had no evidence of disease recurrence or progression after 8 months of follow-up. We propose that term seminal vesicle "mixed epithelial-stromal tumor" be used to designate the tumors of the seminal vesicle containing epithelial and stromal components, with a distinction of grade based on the histologic features and the biological behavior. Histologic features to be evaluated for grade separation include stromal atypia, mitotic activity, nuclear pleomorphism, and tumor necrosis. Designations "low-grade MEST," "intermediate-grade MEST (uncertain malignant potential)," and "high-grade MEST" of seminal vesicle can be applied to these tumors to better characterize and study them in the future.
与前列腺常见肿瘤不同,精囊发生肿瘤性增殖的可能性较低。在罕见的原发性精囊肿瘤中,腺癌最为常见,但也有罕见的精囊肿瘤同时具有上皮和间质成分。这些肿瘤在文献中有各种名称,包括“上皮-间质肿瘤”“囊性上皮-间质肿瘤”“囊腺瘤”“囊肌瘤”“间叶瘤”“苗勒管腺肉瘤样肿瘤”“叶状肿瘤”和“叶状囊肉瘤”。报道的精囊混合上皮-间质肿瘤(MEST)谱系包括低级别、中级别和高级别肿瘤,但这些肿瘤的确切区分和命名仍未确定。基于对已发表病例以及我们实践中的2例索引病例(代表低级别类别)的回顾,我们提出了这些肿瘤的通用命名法。首例患者为46岁男性,因常规直肠检查发现精囊肿瘤。肿瘤最大径为4 cm,完全取代了左侧精囊。肿瘤边界清晰,由多个被梭形细胞间质分隔的囊肿组成。第二例患者为60岁男性,在因前列腺腺癌(Gleason评分3+4,3a期)接受根治性前列腺切除术时偶然发现精囊肿瘤。这两个肿瘤均含有细胞丰富的间质,由均匀的梭形细胞组成,呈束状排列并散布于腺体之间。两个肿瘤均无浸润性边界、细胞异型性、有丝分裂活性增加、出血和坏死等令人担忧的形态学表现。间质细胞雌激素受体、孕激素受体和结蛋白呈阳性。囊肿和扩张的腺体衬覆上皮细胞,细胞角蛋白7呈阳性,前列腺特异性抗原和前列腺特异性酸性磷酸酶呈阴性。首例患者接受了前列腺切除术,随访11年后存活,无疾病复发或进展的证据。同样,第二例患者随访8个月后也无疾病复发或进展的证据。我们建议使用术语“精囊混合上皮-间质肿瘤”来命名含有上皮和间质成分的精囊肿瘤,并根据组织学特征和生物学行为区分级别。用于分级的组织学特征包括间质异型性、有丝分裂活性、核多形性和肿瘤坏死。精囊的“低级别MEST”“中级别MEST(恶性潜能不确定)”和“高级别MEST”等命名可应用于这些肿瘤,以便未来更好地对其进行特征描述和研究。