Mazur M T, Myers J L, Maddox W A
Am J Surg Pathol. 1987 Mar;11(3):210-7. doi: 10.1097/00000478-198703000-00006.
A cystic tumor composed of atypical glands in a cellular stroma arose in the pelvis of a 49-year-old man. Two years later an identical tumor was again excised from the pelvis. Morphologic, immunohistochemical and ultrastructural studies indicate that this neoplasm arose in the seminal vesicle, possibly from a seminal vesicle cyst. The tumor did not involve the prostate gland, and immunohistochemical stains for prostate-specific antigen and prostatic acid phosphatase were negative. Ultrastructural study showed that both the glandular and mesenchymal components of the tumor recapitulated features of normal seminal vesicle, further establishing origin from this site. This tumor resembles the rare cystadenoma of the seminal vesicle, yet the cytologic atypia suggests low grade malignant potential. Following the second excision, the patient has had a disease-free interval of 18 months. Long term follow-up and recognition of additional cases is necessary to define the biologic potential of this unusual tumor.
一名49岁男性盆腔内出现了一个由细胞性间质中的非典型腺体组成的囊性肿瘤。两年后,盆腔内再次切除了一个相同的肿瘤。形态学、免疫组织化学和超微结构研究表明,该肿瘤起源于精囊,可能源自精囊囊肿。肿瘤未累及前列腺,前列腺特异性抗原和前列腺酸性磷酸酶的免疫组织化学染色均为阴性。超微结构研究显示,肿瘤的腺性和间叶性成分均重现了正常精囊的特征,进一步证实了其起源于此部位。该肿瘤类似于罕见的精囊囊腺瘤,但细胞异型性提示具有低级别恶性潜能。第二次切除术后,患者已无病生存18个月。需要长期随访并识别更多病例,以明确这种不寻常肿瘤的生物学潜能。