Taube E T, Denkert C, Pietzner K, Dietel M, Sehouli J, Darb-Esfahani S
Institute of Pathology, Charité University Hospital, Charitéplatz 1, 10117, Berlin, Germany,
Virchows Arch. 2015 Mar;466(3):333-42. doi: 10.1007/s00428-014-1710-7. Epub 2014 Dec 19.
Neuroendocrine differentiation in high-grade serous ovarian carcinomas has only rarely been described. However, in our consultancy experience, we have been pointed at a case of neuroendocrine relapse in a patient with high-grade serous ovarian carcinoma where retrospectively, a minor neuroendocrine component in the primary tumor could be detected. Hypothesizing that immunohistochemical evidence of neuroendocrine differentiation might be more frequent in ovarian carcinoma than suspected by morphology, we immunophenotyped the tissue microarrays (TMAs) of a cohort of 178 high-grade serous carcinomas for chromogranin and synaptophysin expression. Synaptophysin expression was found in 12 (6.7 %) out of 172 patients, and chromogranin A expression was seen in 36 (20.7 %) out of 174 patients. Kaplan-Meier analysis revealed that carcinomas with synaptophysin expression of >20 % of positive cells (n = 4) had a significantly shorter survival time than those with 0-20 % of positive cells (p < 0.0001). Synaptophysin expression remained a significant prognostic factor in multivariate analysis (HR = 10.82, 95 % confidence interval 3.10-37.71, p < 0.0001), independently of age, FIGO stage, and residual tumor after surgery. A trend toward shorter survival was seen in patients with tumors that expressed chromogranin, irrespective of the amount of positive cells (p = 0.173). A neuroendocrine differentiation is important to keep in mind when a neuroendocrine tumor of unknown primary is detected in regional or temporal connection with an ovarian carcinoma. A minor neuroendocrine component in ovarian high-grade serous carcinomas might imply a dismal prognosis.
高级别浆液性卵巢癌中的神经内分泌分化很少被描述。然而,根据我们的咨询经验,我们遇到了一例高级别浆液性卵巢癌患者发生神经内分泌复发的病例,回顾性分析发现原发肿瘤中存在少量神经内分泌成分。鉴于推测神经内分泌分化的免疫组化证据在卵巢癌中可能比形态学所怀疑的更为常见,我们对178例高级别浆液性癌患者的组织微阵列(TMA)进行了嗜铬粒蛋白和突触素表达的免疫表型分析。172例患者中有12例(6.7%)检测到突触素表达,174例患者中有36例(20.7%)检测到嗜铬粒蛋白A表达。Kaplan-Meier分析显示,突触素阳性细胞表达>20%的癌(n = 4)的生存时间明显短于阳性细胞表达为0 - 20%的癌(p < 0.0001)。在多变量分析中,突触素表达仍然是一个显著的预后因素(HR = 10.82,95%置信区间3.10 - 37.71,p < 0.0001),独立于年龄、国际妇产科联盟(FIGO)分期和手术后残留肿瘤。无论阳性细胞数量多少,在表达嗜铬粒蛋白的肿瘤患者中观察到生存时间缩短趋势(p = 0.173)。当在区域或时间上与卵巢癌相关联检测到原发灶不明的神经内分泌肿瘤时,必须牢记神经内分泌分化情况。卵巢高级别浆液性癌中的少量神经内分泌成分可能意味着预后不良。