Department of Pathology, The University of Texas M.D. Anderson Cancer Center, Houston, TX, USA.
Department of Pathology, Stanford University, Stanford, CA, United States.
Pathology. 2018 Feb;50(2):205-213. doi: 10.1016/j.pathol.2017.12.001. Epub 2017 Dec 28.
There have been great strides in our understanding of the serous group of borderline and malignant pelvic epithelial neoplasms in the past decade. While most serous borderline tumours have a favourable prognosis, recurrences and progression to carcinoma occur, often following a protracted clinical course. Clinical and pathological risk factors tend to co-vary, but the presence and type of extraovarian disease is the most important predictor for progression. Progression usually takes the form of low-grade serous carcinoma, although transformation to high-grade carcinoma is occasionally seen. A serous borderline - low-grade serous carcinoma pathway analogous to neoplastic transformation pathways seen in other organ systems has been proposed, based on global gene expression profiling, shared mutations in KRAS or BRAF, and in most cases, the presence of serous borderline tumour in de novo low-grade serous carcinoma. This discussion focuses on the key prognostic factors that predispose to disease progression and/or transformation to carcinoma in serous borderline tumours.
在过去的十年中,我们对浆液性交界性和恶性盆腔上皮性肿瘤有了更深入的了解。虽然大多数浆液性交界性肿瘤预后良好,但仍会出现复发和进展为癌,且通常具有较长的临床过程。临床和病理危险因素往往相互关联,但卵巢外疾病的存在和类型是进展的最重要预测因素。进展通常表现为低级别浆液性癌,但偶尔也会出现高级别癌的转化。基于全球基因表达谱、KRAS 或 BRAF 中的共同突变,以及在大多数情况下,新出现的低级别浆液性癌中存在浆液性交界性肿瘤,提出了类似于其他器官系统中肿瘤发生途径的浆液性交界性-低级别浆液性癌途径。本讨论重点介绍了易导致浆液性交界性肿瘤疾病进展和/或向癌转化的关键预后因素。