Monica Bruno, Larosa Michelangelo, Facchini Francesco, Pozzoli Gianluigi, Franceschetti Ilaria, Piscioli Irene
1Division of Urology, Guastalla Hospital, Guastalla , RE, Italy.
World J Surg Oncol. 2008 Sep 23;6:101. doi: 10.1186/1477-7819-6-101.
The mixed epithelial stromal tumour is morphologically characterised by a mixture of solid and cystic areas consisting of a biphasic proliferation of glands admixed with solid areas of spindle cells with variable cellularity and growth patterns. In previous reports the seminal vesicle cystoadenoma was either considered a synonym of or misdiagnosed as mixed epithelial stromal tumour. The recent World Health Organisation Classification of Tumours considered the two lesions as two distinct neoplasms. This work is aimed to present the low-grade epithelial stromal tumour case and the review of the literature to the extent of establishing the true frequency of the neoplasm.
We describe a low-grade epithelial stromal tumour of the seminal vesicle in a 50-year-old man. Computed tomography showed a 9 x 4.5 cm pelvic mass in the side of the seminal vesicle displacing the prostate and the urinary bladder. Magnetic resonance was able to define tissue planes between the lesion and the adjacent structures and provided useful information for an accurate conservative laparotomic surgical approach. The histology revealed biphasic proliferation of benign glands admixed with stromal cellularity, with focal atypia. After 26 months after the excision the patient is still alive with no evidence of disease.
Cystoadenoma and mixed epithelial stromal tumour of seminal vesicle are two distinct pathological entities with different histological features and clinical outcome. Due to the unavailability of accurate prognostic parameters, the prediction of the potential biological evolution of mixed epithelial stromal tumour is still difficult. In our case magnetic resonance imaging was able to avoid an exploratory laparotomy and to establish an accurate conservative surgical treatment of the tumour.
混合性上皮间质瘤的形态学特征是实性和囊性区域混合存在,由腺体的双相增生与细胞密度和生长模式各异的梭形细胞实性区域组成。在以往的报道中,精囊腺囊腺瘤要么被视为混合性上皮间质瘤的同义词,要么被误诊为混合性上皮间质瘤。最近的世界卫生组织肿瘤分类将这两种病变视为两种不同的肿瘤。这项工作旨在呈现低级别上皮间质瘤病例并回顾文献,以确定该肿瘤的实际发病率。
我们描述了一名50岁男性的精囊低级别上皮间质瘤。计算机断层扫描显示精囊侧有一个9×4.5厘米的盆腔肿块,推移了前列腺和膀胱。磁共振成像能够明确病变与相邻结构之间的组织平面,并为精确的保守性剖腹手术方法提供有用信息。组织学显示良性腺体的双相增生与间质细胞混合,有局灶性异型性。切除术后26个月,患者仍然存活,无疾病证据。
精囊腺囊腺瘤和混合性上皮间质瘤是两种具有不同组织学特征和临床结局的不同病理实体。由于缺乏准确的预后参数,预测混合性上皮间质瘤的潜在生物学演变仍然困难。在我们的病例中,磁共振成像能够避免剖腹探查,并确立对该肿瘤的精确保守手术治疗。