Martorana Eugenio, Micali Salvatore, Pirola Giacomo Maria, Reggiani Bonetti Luca, Clò Vera, Ghaith Ahmed, Bianchi Giampaolo
Department of Urology, University of Modena, Modena - Italy.
Department of Pathology, University of Modena, Modena - Italy.
Urologia. 2016 Sep 26;83(3):163-167. doi: 10.5301/uro.5000174. Epub 2016 May 6.
Ductal adenocarcinoma is a rare subtype of prostate cancer with a worse prognosis.Histologically, it is characterized by the presence of tall, pseudostratified columnar epithelium with abundant cytoplasm organized in a papillary or cribriform-papillary pattern. Several clinical differences distinguish this subtype of prostate cancer by the conventional acinar adenocarcinoma: exophytic growth into the prostatic urethra, different clinical presentation, different sites of metastasis and more aggressiveness. The rarity of this tumour forced to base our knowledge on small case series or on individual case reports, and does not help to establish appropriate guidelines. Therefore, the diagnosis of this tumour masks clinical implications that are still not well-understood.We report the case of a 69-year-old Caucasian man with a diagnosis of pure prostate ductal adenocarcinoma that early developed multiple metastases after radical prostatectomy. The patient started hormonal therapy with a fast biochemical and radiologic (positron emission tomography-computed tomography, PET-CT) hormonal escape. Therefore, we took the decision to perform chemotherapy with Taxotere along with prednisolone with a relative stability of prostate-specific antigen (PSA) level, but a new PET-CT scan showed a further progression of the disease. Finally, the patient underwent therapy with Abiraterone acetate that did not stop the cancer progression.No therapeutic options available showed a good control of disease progression. PSA proved to be a poor marker while, on the contrary, PET-CT scan has proved to be particularly useful in the management of the disease progression. More efforts are required to add new knowledge about this tumour and assess what is known until now.
导管腺癌是前列腺癌的一种罕见亚型,预后较差。在组织学上,其特征是存在高柱状、假复层柱状上皮,细胞质丰富,呈乳头状或筛状乳头状模式排列。这种前列腺癌亚型与传统的腺泡腺癌在临床上有几个不同之处:向前列腺尿道外生性生长、临床表现不同、转移部位不同以及侵袭性更强。这种肿瘤的罕见性使得我们只能基于小病例系列或个别病例报告来了解相关知识,无助于制定合适的指南。因此,这种肿瘤的诊断掩盖了一些尚未被充分理解的临床意义。我们报告了一例69岁的白种男性患者,诊断为纯前列腺导管腺癌,在根治性前列腺切除术后早期发生了多处转移。患者开始接受激素治疗,但很快出现生化和影像学(正电子发射断层扫描-计算机断层扫描,PET-CT)激素抵抗。因此,我们决定使用多西他赛联合泼尼松龙进行化疗,前列腺特异性抗原(PSA)水平相对稳定,但新的PET-CT扫描显示疾病进一步进展。最后,患者接受了醋酸阿比特龙治疗,但未能阻止癌症进展。现有的治疗方案均未能有效控制疾病进展。PSA被证明是一个较差的标志物,相反,PET-CT扫描在疾病进展管理中已被证明特别有用。需要做出更多努力来增加关于这种肿瘤的新知识,并评估目前已知的情况。