Peverelli Giorgia, Grassi Paolo
Medical Oncology Department, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan - Italy.
Tumori. 2017 Nov 15;103(Suppl. 1):e56-e59. doi: 10.5301/tj.5000651.
Pure small cell neuroendocrine carcinoma of the prostate is a rare entity characterized by a poor prognosis due to early metastatic spread as well as resistance to treatment. Considering its increasing occurrence, clinicians should be aware of its aggressive behavior, the relevance of an early diagnosis, and proper management.
A 71-year-old man treated with brachytherapy for localized low-risk prostate cancer developed widespread disease 7 years later with a prostate-specific antigen-negative neuroendocrine small cell phenotype. He was also diagnosed with syndrome of inappropriate antidiuretic hormone secretion (SIADH) soon after starting chemotherapy.
A substantial radiologic and clinical response to chemotherapy was observed and the paraneoplastic SIADH was successfully treated with oral vaptan therapy.
Secondary small cell prostate carcinoma is an underestimated entity with high sensitivity to chemotherapy, although a standard treatment has not yet been defined. Moreover, oral vaptans demonstrated prompt efficacy and simple management in correcting SIADH-related hyponatremia.
前列腺纯小细胞神经内分泌癌是一种罕见的疾病,其特征是由于早期转移扩散以及对治疗的抵抗而导致预后不良。鉴于其发病率不断上升,临床医生应了解其侵袭性、早期诊断的相关性以及适当的管理方法。
一名71岁男性因局限性低风险前列腺癌接受近距离放射治疗,7年后出现广泛病变,具有前列腺特异性抗原阴性的神经内分泌小细胞表型。他在开始化疗后不久还被诊断出患有抗利尿激素分泌不当综合征(SIADH)。
观察到化疗有显著的放射学和临床反应,副肿瘤性SIADH通过口服血管加压素受体拮抗剂治疗成功治愈。
继发性小细胞前列腺癌是一种被低估的疾病,对化疗高度敏感,尽管尚未确定标准治疗方法。此外,口服血管加压素受体拮抗剂在纠正SIADH相关低钠血症方面显示出迅速的疗效和简单的管理方法。